US20100042168A1 - Electronic system for influencing cellular functions in a warm-blooded mammalian subject - Google Patents

Electronic system for influencing cellular functions in a warm-blooded mammalian subject Download PDF

Info

Publication number
US20100042168A1
US20100042168A1 US12/450,450 US45045008A US2010042168A1 US 20100042168 A1 US20100042168 A1 US 20100042168A1 US 45045008 A US45045008 A US 45045008A US 2010042168 A1 US2010042168 A1 US 2010042168A1
Authority
US
United States
Prior art keywords
frequencies
amplitude
amplitude modulation
frequency
control information
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/450,450
Inventor
Boris Pasche
Alexandre Barbault
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
THERABIONIC LLC
Original Assignee
Boris Pasche
Alexandre Barbault
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Boris Pasche, Alexandre Barbault filed Critical Boris Pasche
Publication of US20100042168A1 publication Critical patent/US20100042168A1/en
Assigned to THERABIONIC, LLC reassignment THERABIONIC, LLC ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BARBAULT, ALEXANDRE, MR., PASCHE, BORIS, MR.
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/40Applying electric fields by inductive or capacitive coupling ; Applying radio-frequency signals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/02Radiation therapy using microwaves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/02Radiation therapy using microwaves
    • A61N5/022Apparatus adapted for a specific treatment

Definitions

  • This invention relates to an electronic system for influencing cellular functions in a warm-blooded mammalian subject. More particularly, the invention concerns research findings related to how earlier electronic systems may be modified and programmed to achieve both improved and additional therapeutic effects.
  • the direct or indirect influence on cancerous cell growth may involve but is not necessarily limited to any of prophylactic avoidance of cancerous cell formation, influencing of cell functions such as for example influencing leukocyte cell functions which can lead to inhibition of cancerous cell growth or proliferation thereof, and/or killing of cancerous cells harboured by a warm-blooded mammalian subject.
  • Electromagnetic energy generating devices and use of electromagnetic energies for treating living mammalian subjects harbouring cancerous cells described in the literature include: U.S. Pat. No. 5,908,441 issued Jun. 1, 1999 to Bare; James E. and the references cited therein and so-called “NovoCure technology” involving in vivo implantation of electrodes to either side of tumorous growths.
  • This literature does not contemplate very low energy emissions of electromagnetic energy involving amplitude-modulated high frequency carrier signals as required in terms of the present invention.
  • U.S. Pat. No. 5,690,692 issued on Nov. 25, 1997 entitled “Bio-Active Frequency Generator and Method” describes a programmable control which instructs a frequency synthesizer to enable generation of an electrical current at a specific precise frequency signal or at a series of specific precise frequencies signals having a square wave form to within an accuracy of 0.001 Hz.
  • This Patent contemplates amplifying the voltage of the generated signals and applying the signals to a subject at the specific precise frequency or sequentially at the series of specific precise frequencies by means of electrodes held by or otherwise connected to the subject (which may be a mammal or a food).
  • this Patent does not contemplate very low energy emissions involving amplitude-modulated high frequency carrier signals as required in terms of the present invention.
  • an electronic system which is activatable by electrical power.
  • the system is employed to influence cellular functions or malfunctions in a warm-blooded mammalian subject.
  • the system comprises one or more controllable low energy electromagnetic energy generator circuits for generating one or more high frequency radio frequency RF carrier signals.
  • One or more microprocessors or integrated circuits comprising or communicating with the one or more generator circuits are provided which are also for receiving control information from a source of programmed control information.
  • the one or more generator circuits include one or more amplitude modulation control signal generators for controlling amplitude modulated variations of the one or more high frequency carrier signals.
  • the one or more generator circuits furthermore include one or more programmable amplitude modulation frequency control signal generators for controlling the frequency at which the amplitude modulations are generated.
  • the one or more amplitude modulation frequency control generators are, in terms of an important improvement of the present invention, adapted to accurately control the frequency of the amplitude modulations to within an accuracy of at least 1000 ppm relative to one or more determined or predetermined reference amplitude modulation frequencies selected from within a range of 0.01 Hz to 150 kHz.
  • the system furthermore comprises a connection or coupling position for connection or coupling to or being connected or coupled to an electrically conductive applicator for applying to the warm-blooded mammalian subject the one or more amplitude-modulated low energy emissions at said accurately controlled modulation frequencies.
  • the term, “accurately controlled” means that the modulated low energy electromagnetic emissions should be modulated to within a resolution of at most about 1 Hz of intended higher frequencies (greater than about 1000 Hz) determined or predetermined modulation frequencies. For example, if one of the one or more determined or predetermined modulation frequencies to be applied to the warm-blooded mammalian subject is about 2000 Hz, the accurate control should lead to such modulated low energy emission being generated at a frequency of between about 1999 and about 2001 Hz.
  • the accurate control should lead to a resolution of about 0.5, more preferably about 0.1, yet more preferably about 0.01 and indeed most preferably about 0.001 Hz of the intended determined or predetermined modulation frequency.
  • the specific absorption rate should be and is most preferably substantially less than 1.6 milliW/g weight of living tissue.
  • the system includes a microprocessor (which may more recently be replaced by an integrated circuit) into which control information is loaded from an application storage device.
  • the microprocessor (or now alternatively integrated circuit) then controls the function of the system to produce the desired therapeutic emissions.
  • an impedance transformer connected intermediate the emitter of low energy electromagnetic emissions and a probe (here more broadly described as an electrically conductive applicator) for applying the emissions to the patient.
  • the impedance transformer substantially matches the impedance of the patient seen from the emitter circuit with the impedance of the output of the emitter circuit.
  • FIG. 1 shows an exemplary casing structure for the electronic circuit shown in FIG. 2 , an applicator 13 (exemplified as a probe suitable for being placed in the mouth of a patient) and an interface 16 (which may be replaced by a receiver) for receiving information from a source of information 52 such as may be comprised in an information storage device, e.g. of the nature described and illustrated in FIGS. 12 to 17 of EP 0 592 851 B1.
  • a source of information 52 such as may be comprised in an information storage device, e.g. of the nature described and illustrated in FIGS. 12 to 17 of EP 0 592 851 B1.
  • FIG. 2 is a block diagram of exemplary circuitry which may be comprised in the exemplary casing structure of FIG. 1 .
  • This FIG. 2 differs essentially from FIG. 2 of EP 0 592 851 B1 by comprising a highly accurate modulation frequency generator 31 (named a Digital Direct Synthesizer or DDS), which enables accurate control of modulatable oscillator represented by dotted line block 106 .
  • DDS Digital Direct Synthesizer
  • FIG. 3 of EP 0 592 851 B1 is a detailed schematic of a modulation signal generator 31, replaced by a DDS modulation frequency generator 31 comprised in the circuit of present FIG. 2 ;
  • FIG. 4 of EP 0 592 851 B1 is a detailed schematic of a modulation signal buffer and carrier oscillator circuit which may be employed in the circuit of the present FIG. 2 ;
  • FIG. 5 of EP 0 592 851 B1 is a detailed schematic example of an amplitude modulation (AM) and power generator 34 and output filter 39 which could be comprised in the circuit of the present FIG. 2 ;
  • AM amplitude modulation
  • FIG. 6 of EP 0 592 851 B1 is a detailed schematic example of an impedance transformer 14 which may be comprised in the circuit of the present FIG. 2 ;
  • FIG. 7 of EP 0 592 851 B1 is a detailed schematic example of an emission sensor 53 which may be comprised in the circuit of the present FIG. 2 ;
  • FIG. 8 of EP 0 592 851 B1 is a detailed schematic example of an output power sensor circuit 54 which may be employed in the circuit of the present FIG. 2 .
  • FIG. 9 of EP 0 592 851 B1 is a detailed schematic example of a display module or information output 17 which may be included in the circuit of the present FIG. 2 .
  • FIG. 10 of EP 0 592 851 B1 is a detailed schematic example of a power supply control circuit including battery charger 57 which may be comprised in the circuit of the present FIG. 2 .
  • FIGS. 11a-d of EP 0 592 851 B1 are exemplary flow charts of the method of operation of the system of FIGS. 1 and 2 .
  • FIG. 1 presented is a modulated low energy electromagnetic emission application system 11 , in accordance with the present invention.
  • a modulated low energy electromagnetic emission application system 11 As described in prior U.S. Pat. Nos. 4,649,935 and 4,765,322, such a system has proven to be useful in the practice of Low Energy Emission Therapy (LEET, a trademark of Symtonic S.A. or a successor of this Company), which involves application of emissions of low energy radio frequency (RF) electromagnetic waves to a warm-blooded mammalian subject.
  • LEET Low Energy Emission Therapy
  • RF radio frequency
  • the application has proven to be an effective mode of treating a warm-blooded mammalian subject suffering from central nervous system (CNS) disorders such as, for example, generalized anxiety disorders, panic disorders, sleep disorders including insomnia, psychiatric disorders such as depression, obsessive compulsive disorders, disorders resulting from substance abuse, sociopathy, post traumatic stress disorders or other disorders of the central nervous system and combinations thereof.
  • CNS central nervous system
  • the system includes an electrically conductive applicator 12 , 13 for applying one or more electromagnetic emissions to the warm-blooded mammalian subject.
  • One form of applicator may consist of an electrically conductive probe or mouthpiece 13 which is inserted into the mouth of a subject undergoing treatment. Probe 13 is connected to an electromagnetic energy emitter (see also FIG. 2 ), through coaxial cable 12 and impedance matching transformer 14 .
  • An example of a coupling found to be effective involving indirect physical contact with the skin of a patient is an insulated applicator to be placed over or within an ear of the patient.
  • the emissions thus passed to the patient may be either by capacitive or radiated means or by a combination of both.
  • Electronic system 11 also includes a connector or coupler for connection to a programmable device such as a computer or an interface or receiver 16 which is adapted to receive an application storage device 52 such as, for example, magnetic media, semiconductor media, optical media or mechanically encoded media, or programmed emissions programmed with control information employed to control the operation of system 11 so that the desired type of low energy emission therapy is applied to the patient.
  • a programmable device such as a computer or an interface or receiver 16 which is adapted to receive an application storage device 52 such as, for example, magnetic media, semiconductor media, optical media or mechanically encoded media, or programmed emissions programmed with control information employed to control the operation of system 11 so that the desired type of low energy emission therapy is applied to the patient.
  • Application storage device 52 can be provided with a microprocessor which, when applied to interface 16 , operates to control the function of system 11 to apply the desired low energy emission therapy.
  • application storage device 52 can be provided with a microprocessor which is used in combination with microprocessor 21 within system 11 .
  • the microprocessor within device 52 could assist in the interfacing of storage device 52 with system 11 , or could provide security checking functions.
  • System 11 may also include a display 17 which can display various indications of the operation of system 11 .
  • system 11 may include on and off power buttons 18 and 19 , optionally replaced by user interface 21 A (refer to FIG. 2 ).
  • FIG. 2 presented is a block diagram of exemplary electronic circuitry of system 11 , in accordance with the present invention.
  • a data processor such as for example, microprocessor or integrated circuit 21 , operates as the controller for electronic system 11 , and is connected to control the various components of the system 11 , for example, through address bus 22 , data bus 23 and input/output lines 25 .
  • the block diagram of FIG. 2 is modified as compared to FIG. 2 of EP 0 592 851 B1 by including what is known as a digital direct synthesizer (DDS) 31 which operates as a accurate and stable modulation frequency generator within the system 11 .
  • DDS digital direct synthesizer
  • An exemplary DDS device is available from Analog Devices of Norwood, Mass. 02062-9106, USA, Part No AD9835.
  • the device is a numerically controlled oscillator and modulation capabilities are provided for phase modulation and frequency modulation.
  • dotted line block 102 entitled “PROCESSOR WITH DAC”, the functionality of the DDS may also be combined with microprocessor 21 with digital to analogue converter (DAC).
  • DAC digital to analogue converter
  • Microprocessor 21 preferably includes internal storage for the operation of a coded control program, and temporary data.
  • microprocessor 21 may include input/output ports and internal timers.
  • Microprocessor 21 may be a microcontroller, for example microcontrollers 8048 or 8051 available from Intel Corporation of Santa Clara, Calif. 95054-1549, USA.
  • microprocessor 21 The timing for microprocessor 21 is provided by system clock oscillator 26 A which may be run at any clock frequency suitable for the particular type of microprocessor used.
  • An exemplary clock frequency is about 8.0 MHz.
  • Oscillator 26 A may be replaced by reference frequency oscillator 26 which secures the stability of the accurate modulation frequency.
  • RF (radio frequency) oscillator 32 may also be employed for this purpose.
  • a combination of oscillators is represented by dotted line block 104 , entitled “OSCILLATOR”.
  • microprocessor 21 functions to control controllable electromagnetic energy generator circuit 29 to produce a desired form of modulated low energy electromagnetic emission for application to a subject through applicator or probe 13 .
  • Dotted line block 29 entitled CONTROLLABLE GENERATOR, includes DDS modulation frequency generator 31 and carrier signal oscillator 32 .
  • Microprocessor 21 operates to activate or deactivate controllable generator circuit 29 through oscillator disable line 33 , as described in greater detail in EP 0 592 851 B1.
  • Controllable generator circuit 29 also includes an AM modulator and power generator 34 which operates to amplitude modulate a carrier signal produced by carrier oscillator 32 on carrier signal line 36 , with a modulation signal produced by modulation signal generator circuit 31 on modulation signal line 37 .
  • the combination of the functionality of the DDS modulation frequency generator 31 , with processor 21 with DAC, represented by dotted line block 102 enables output lines 33 and 37 to be combined to produce a single signal. The combination furthermore enables arbitrary or periodic wave forms of any shape to be generated, as similarly described in EP 0 592 851 B1.
  • AM modulator and power generator 34 produces an amplitude modulated carrier signal on modulated carrier signal line 38 , which is then applied to emitter output filter circuit 39 .
  • the filter circuit 39 is connected to probe or applicator 13 via power emission sensor 54 , coaxial cable 12 and impedance transformer 14 .
  • Microprocessor 21 controls DDS modulation signal generator circuit 31 of controllable generator circuit 29 via interface lines 25 .
  • microprocessor 21 may select a desired waveform stored in a modulation waveform storage device 43 and also controls a waveform address generator 41 to produce on waveform address bus 42 a sequence of addresses which are applied to modulation signal storage device 43 in order to retrieve the selected modulation signal.
  • the desired modulation signal is retrieved from modulation signal storage device 43 and applied to modulation signal bus 44 in digital form.
  • Modulation signal bus 44 is applied to wave form generator and DAC 46 which converts the digital modulation signal into analogue form.
  • This analogue modulation signal is then applied to a selective filter 47 which, under control of microprocessor 21 , filters the analogue modulation signal by use of a variable filter network including resistor 48 and capacitors 49 and 51 in order to smooth the wave form produced by DAC 46 on modulation signal line 20 .
  • a further embodiment possibility is a combination of PROCESSOR WITH DAC dotted line block 102 with OSCILLATOR dotted line block 104 or with a combination of oscillators 26 and 26 A.
  • the hardware solution described in EP 0 592 851 B1 can be realized internally in the processor 102 with multiple outputs 33 and 37 or a single output combining these signals.
  • the particular modulation control information employed by microprocessor 21 to control the operation of controllable generator circuit 29 is stored in application storage device 52 .
  • the application storage device is conveniently a computer comprising or being for receiving the information.
  • application storage devices illustrated and described in EP 0 592 851 B1, with reference to FIGS. 12, 13, 14 and 15, may be selected.
  • Interface 16 is configured as appropriate for the particular application storage device 52 in use. Interface 16 translates the control information stored in application storage device 52 into a usable form for storage within the memory of microprocessor 21 to enable microprocessor 21 to control controllable generator circuit 29 to produce the desired modulated low energy emission.
  • Interface 16 may directly read the information stored on application storage device 52 , or it may read the information through use of various known communication links. For example, radio frequency, microwave, laser, telephone, internet or optical based communications links may be employed to transfer information between interface or receiver 16 and application storage device or computer 52 .
  • the system 11 may comprise a user identification device, included in block 21 a in FIG. 2 . Conveniently, such a device communicates with the one or more data processors or integrated circuits 21 via interface 16 , as shown.
  • the user identification device may be of any type, a finger print reader being an example. Such a reader is for example available from Lenovo, 70563 Stuttgart, Germany, Part No. 73P4774.
  • control information stored in application storage device or computer 52 specifies various controllable parameters of the modulated low energy RF electromagnetic emission to be applied to a subject through applicator or probe 13 .
  • controllable parameters include, for example, but are not necessarily limited to, the frequency and amplitude of the carrier, the amplitudes and frequencies and wave forms of the modulation of the carrier, the duration of the emission, the power level of the emission, the duty cycle of the emission (i.e., the ratio of on time to off time of pulsed emissions applied during a treatment), the sequence of application of different modulation frequencies for a particular application, and the total number of treatments and duration of each treatment prescribed for a particular subject, and combinations thereof.
  • the carrier signal and modulation signal may be selected to drive the applicator or probe 13 with an amplitude modulated signal in which the carrier signal includes spectral frequency components below about 1 GHz, and preferably between about 1 MHz and about 900 MHz, and in which the modulation signal comprises spectral frequency components between about 0.01 Hz and 150 KHz.
  • the one or more modulation frequencies may be simultaneously emitted or sequenced to form the modulation signal.
  • an electromagnetic emission sensor 53 may be provided to detect the presence of electromagnetic emissions at the frequency of the carrier oscillator 32 .
  • Emission sensor 53 provides microprocessor 21 with an indication of whether or not electromagnetic emissions at the desired frequency are present.
  • Microprocessor 21 then takes appropriate action, for example, by displaying an error message on display 17 , disabling controllable generator circuit 29 , or the like.
  • a power sensor 54 is preferably included which detects the amount of power applied to the subject through applicator or probe 13 compared to the amount of power returned or reflected from the subject. This ratio is indicative of the proper use of the system during a therapeutic session. Power sensor 54 applies to microprocessor 21 , through power sensor line 56 , an indication of the amount of power applied to patient through applicator or probe 13 relative to the amount of power reflected from the patient.
  • the indication provided on power sense line 56 may be digitalized and employed by microprocessor 21 , for example, to detect and control a level of applied power, and to record on application storage device 52 information related to the actual treatments applied to and received by the patient. Such information may then be used by a physician or other clinician to assess patient treatment compliance and effect.
  • treatment information may include, for example: the number of treatments applied for a given time period; the actual time and date of each treatment; the number of attempted treatments; the treatment compliance (i.e., whether the applicator or probe was in place or not during the treatment session); and the cumulative dose of a particular modulation frequency.
  • the level of power applied is preferably controlled to cause the specific absorption rate (SAR) of energy absorbed by the patient to be from about 1 microWatt per kilogram of tissue to about 50 Watts per kilogram of tissue.
  • the power level is controlled to cause an SAR of from about 100 microWatts per kilogram of tissue to about 10 Watts per kilogram of tissue.
  • the power level is controlled to cause an SAR of from about 1 milliWatt per kilogram of tissue to about 100 milliWatts per kilogram of tissue.
  • SARs may be in any tissue of the patient, but are preferably in the tissue of the central nervous system or the diseased tissue.
  • System 11 may also include powering circuitry including battery and charger circuit 57 and battery voltage change detector 58 .
  • the RF carrier oscillator 32 produces a RF carrier frequency of about 27 MHz.
  • Other embodiments of the invention contemplate RF carrier frequencies of about 48 MHz, about 433 MHz or about 900 MHz.
  • the RF carrier frequency produced by carrier oscillator 32 has spectral frequency components less than about 1 GHz and preferably between about 1 MHz and about 916 MHz.
  • the carrier frequency produced by carrier oscillator 32 may be variable and controllable by microprocessor 21 by use of stored or transmitted control information.
  • Carrier oscillator 32 produces on carrier signal line 36 a carrier signal which is then modulated by the modulation signal carried on signal line 37 .
  • Oscillator disable line 33 enables microprocessor 21 to disable the signal from oscillator 32 by applying an appropriate disable signal to oscillator disable line 33 .
  • the output of the AM modulator and power generator 34 appears on signal line 38 .
  • This modulated signal is applied through emitter output filter 39 which substantially reduces or eliminates the carrier harmonics resulting from side effects of the modulator and power generator circuit 34 .
  • the output of the AM modulator and power generator 34 and emitter output filter 39 may be designed to possess a 50 Ohm output impedance to match a 50 Ohm impedance of coaxial cable 12 .
  • Impedance transformer 14 serves to match this complex impedance with the 50 Ohm impedance of coaxial cable 12 and therefore the output impedance of the AM modulator 34 and output filter 39 . This promotes power transmission, and minimizes reflections.
  • a contact probe with coupling to the mucosa of the mouth has been optimized for a contact probe with coupling to the mucosa of the mouth.
  • a conductive, isolated probe has been used at a frequency around 433 MHz coupling to the outer ear channel. Due to the different probe design in such a frequency band and with this coupling method, the values of matching elements (79 and 81 described in EP 0592 851 B1) would be different or could even be omitted.
  • Applicator or probe 13 may then be regarded as a capacitive coupler or as an antenna matched to the capacitive load.
  • microprocessor 21 may operate to analyse the signal appearing on power sense line 56 to determine and control the amount of power applied to the patient, and to assess patient treatment compliance, and possibly to record indicia of the patient treatment compliance on application storage device 52 for later analysis and assessment by a physician or other clinician.
  • Exemplary of treatments performed on patients have included brain, bladder, colorectal, kidney, mesothelium, neuroendocrine, liver, lung, breast, ovary, pancreas, prostate and thyroid tumour types.
  • the treatments involved applying an about 27.12 MHz RF signal, amplitude modulated at specifically defined frequencies ranging from about 0.2 to about 23,000 Hz at very high precision and stability. Further Examples of treatment modes (at specific accurately controlled AM frequencies) for specified types of tumours are described in detail below.
  • a phase I study was conducted consisting of three daily 40 min treatments. From March 2004 to September 2006, 24 patients with advanced solid tumors were enrolled. The median age was 57.0 ⁇ 12.2 years. 16 patients were female. As of January 2007, 5 patients are still on therapy, 13 patients died of tumor progression, 2 patients are lost to follow-up and one patient withdrew consent. The most common tumor types were breast (7), ovary (5) and pancreas (3). 22 patients had received prior systemic therapy and 16 had documented tumor progression prior to study entry.
  • patients with progressive disease at study entry one had a partial response for >14.4 weeks associated with >50% decrease in CEA, CA 125 and CA 15-3 (previously untreated metastatic breast cancer); one patient had stable disease for 34.6 weeks (add info); one patient had a 50% decrease in CA 19-9 for 12.4 weeks (recurrent pancreatic cancer).
  • Phase I data suggest that low levels of electromagnetic fields amplitude-modulated at specific frequencies administered intrabucally with the device of Example A are a safe and potentially effective treatment for advanced cancer.
  • the device emits a 27.12 MHz RF signal, amplitude-modulated with cancer-specific frequencies ranging from 0.2 to 23,000 Hz with high precision.
  • the device is connected to a spoon-like coupler placed in the patient's mouth during treatment. Patients with advanced hepatocellular carcinoma HCC and limited therapeutic options were offered treatment with a combination of HCC-specific frequencies.
  • the electronic device of the present invention comprising means for the accurate control over the frequencies and stability of amplitude modulations of a high frequency carrier signal, provides a safe and promising novel treatment modality for the treatment of patients suffering from various types of advanced forms of cancer.
  • Exemplary of above accurately controlled amplitude modulated frequencies controlling the frequency of amplitude modulations of a high frequency carrier signal are set forth below along with the type of cancer or tumour harboured by a subject to be treated.
  • the above Examples reflect AM frequencies determined by a bio-feedback procedure involving very substantial observations and measurements of physiological responses (at certain well defined AM frequencies) by subjects exposed to low energy electromagnetic emission excitation. In general, it is recommended that all of the listed frequencies be applied in the treatment of subjects suffering from the indicated form of cancer. However, a limited number of the listed frequencies also lead to beneficial effects.
  • the electronic system of the present invention may be adapted to screen a subject for physiological responses over a broad range of frequencies to determine the presence or absence tumour cells and, if positive, then to note at which defined frequencies physiological responses are elicited.
  • These frequencies will in general match with the defined frequencies listed in one or other of the Examples above or such further examples as may be developed and hence the nature of the tumour will be known.
  • the electronic system of the invention is therefore a valuable diagnostic tool for diagnosing the presence or absence and identities of types of tumour cell growths or cancers. Furthermore, the electronic system of the invention is of value for predicting whether a patient will benefit from the application of a given series of modulation frequencies. The system therefore possesses a capability of predicting responses to treatment, thereby enhancing the possibility to select optimal modes of treatment.
  • the sequence of well defined frequencies are preferably applied sequentially for determined periods of time, e.g. 3 seconds for each frequency, but several frequencies may also be applied simultaneously. This means that a cycle of application involving 180 frequencies would take nearly 10 minutes time. Advantageous effects may however also arise from applying individual well defined frequencies for differing time periods, e.g. some for 3 seconds, some for 6 seconds, etc. . . . .
  • Therapeutic dosages to be applied to a subject suffering from the presence of tumour cell growth or cancer are determined by the time of application of the low energy electromagnetic emissions to the subject and will depend on the nature of the cancer and the overall condition of the subject. In general, however, greatest experience has been gained in treating terminally ill subjects expected to survive no longer than about three months and who have agreed to discontinue alternative forms of cancer treatments such as chemo-therapy or radioactive treatment. In these severe cases, lengthy times of treatment are recommended, e.g. 3 times 1 hour daily treatment.
  • alternative forms of application i.e. other than by means of a mouth probe, continuous application is possible and is likely to enhance compliance and the efficacy of the treatment.

Abstract

An electronic system activatable by electrical power is described. The system is useful for influencing cellular functions or malfunctions in a warm-blooded mammalian subject. The system includes one or more controllable low energy HF (High Frequency) carrier signal generator circuits, one or more data processors for receiving control information, one or more amplitude modulation control generators and one or more amplitude modulation frequency control generators. The amplitude modulation frequency control generators are adapted to accurately control the frequency of the amplitude modulations to within an accuracy of at least 1000 ppm, most preferably to within about 1 ppm, relative to one or more determined or predetermined reference amplitude modulation frequencies.

Description

    FIELD OF THE INVENTION
  • This invention relates to an electronic system for influencing cellular functions in a warm-blooded mammalian subject. More particularly, the invention concerns research findings related to how earlier electronic systems may be modified and programmed to achieve both improved and additional therapeutic effects.
  • BACKGROUND OF THE INVENTION
  • Reference is made to European Patent EP 0 592 851 B1 and corresponding Patents and Patent Applications and to the various publications referred to therein. Since the time of the priority Application filed in the USA on 25 Sep. 1992 (U.S. Ser. No 951,563 now U.S. Pat. No. 5,441,528), a number of further publications related to effects of very low energy electromagnetic fields on patients suffering from insomnia and/or anxiety disorders have taken place:
    • Koziol J A, Erman M, Pasche B, Hajdukovic R, Mitler MM (1993) Assessing a changepoint in a sequence of repeated measurements with application to a low-energy emission therapy sleep study. J Applied Statistics 20: 393-400
    • Amato D, Pasche B (1993) An evaluation of the safety of low energy emission therapy. Compr Ther 19: 242-247
    • Higgs L, Reite M, Barbault A, Lebet J P, Rossel C, Amato D, Dafni U, Pasche B (1994) Subjective and Objective Relaxation Effects of Low Energy Emission Therapy. Stress Medicine 10: 5-13
    • Reite M, Higgs L, Lebet J P, Barbault A, Rossel C, Kuster N, Dafni U, Amato D, Pasche B (1994) Sleep Inducing Effect of Low Energy Emission Therapy. Bioelectromagnetics 15: 67-75
    • Lebet J P, Barbault A, Rossel C, Tomic Z, Reite M, Higgs L, Dafni U, Amato D, Pasche B (1996) Electroencephalographic changes following low energy emission therapy. Ann Biomed Eng 24: 424-429
    • Pasche B, Erman M, Hayduk R, Mitler M, Reite M, Higgs L, Dafni U, Amato D, Rossel C, Kuster N, Barbault A, Lebet J-P (1996) Effects of Low Energy Emission Therapy in chronic psychophysiological insomnia. Sleep 19: 327-336
    • Kelly T L, Kripke D F, Hayduk R, Ryman D, Pasche B, Barbault A (1997) Bright light and LEET effects on circadian rhythms, sleep and cognitive performance. Stress Medicine 13: 251-258
    • Pasche B, Barbault A (2003) Low-Energy Emission Therapy: Current Status and Future Directions. In Bioelectromagnetic Medicine, Rosch P J, Markov M S (eds) pp 321-327. Marcel Dekker, Inc.: New York, N.Y.
  • The above publications are related to an earlier device, system and use thereof described in said EP 0 592 851 B1. The improved electronic system and programmed control thereof in accordance with the present invention, however, has been determined to find therapeutic application not only for influencing cellular functions (or malfunctions) leading to central nervous system (CNS) disorders, but more particularly for influencing other cellular functions (or malfunctions) including directly or indirectly influencing cancerous cell growth or proliferation thereof in warm-blooded mammalian subjects. The direct or indirect influence on cancerous cell growth may involve but is not necessarily limited to any of prophylactic avoidance of cancerous cell formation, influencing of cell functions such as for example influencing leukocyte cell functions which can lead to inhibition of cancerous cell growth or proliferation thereof, and/or killing of cancerous cells harboured by a warm-blooded mammalian subject.
  • Electromagnetic energy generating devices and use of electromagnetic energies for treating living mammalian subjects harbouring cancerous cells described in the literature include: U.S. Pat. No. 5,908,441 issued Jun. 1, 1999 to Bare; James E. and the references cited therein and so-called “NovoCure technology” involving in vivo implantation of electrodes to either side of tumorous growths. This literature however does not contemplate very low energy emissions of electromagnetic energy involving amplitude-modulated high frequency carrier signals as required in terms of the present invention.
  • U.S. Pat. No. 5,690,692 issued on Nov. 25, 1997 entitled “Bio-Active Frequency Generator and Method” describes a programmable control which instructs a frequency synthesizer to enable generation of an electrical current at a specific precise frequency signal or at a series of specific precise frequencies signals having a square wave form to within an accuracy of 0.001 Hz. This Patent contemplates amplifying the voltage of the generated signals and applying the signals to a subject at the specific precise frequency or sequentially at the series of specific precise frequencies by means of electrodes held by or otherwise connected to the subject (which may be a mammal or a food). Once again, this Patent does not contemplate very low energy emissions involving amplitude-modulated high frequency carrier signals as required in terms of the present invention.
  • SUMMARY OF THE INVENTION
  • In one aspect of the invention, an electronic system is provided which is activatable by electrical power. The system is employed to influence cellular functions or malfunctions in a warm-blooded mammalian subject. The system comprises one or more controllable low energy electromagnetic energy generator circuits for generating one or more high frequency radio frequency RF carrier signals. One or more microprocessors or integrated circuits comprising or communicating with the one or more generator circuits are provided which are also for receiving control information from a source of programmed control information. The one or more generator circuits include one or more amplitude modulation control signal generators for controlling amplitude modulated variations of the one or more high frequency carrier signals. The one or more generator circuits furthermore include one or more programmable amplitude modulation frequency control signal generators for controlling the frequency at which the amplitude modulations are generated. The one or more amplitude modulation frequency control generators are, in terms of an important improvement of the present invention, adapted to accurately control the frequency of the amplitude modulations to within an accuracy of at least 1000 ppm relative to one or more determined or predetermined reference amplitude modulation frequencies selected from within a range of 0.01 Hz to 150 kHz. The system furthermore comprises a connection or coupling position for connection or coupling to or being connected or coupled to an electrically conductive applicator for applying to the warm-blooded mammalian subject the one or more amplitude-modulated low energy emissions at said accurately controlled modulation frequencies.
  • As used herein, the term, “accurately controlled” means that the modulated low energy electromagnetic emissions should be modulated to within a resolution of at most about 1 Hz of intended higher frequencies (greater than about 1000 Hz) determined or predetermined modulation frequencies. For example, if one of the one or more determined or predetermined modulation frequencies to be applied to the warm-blooded mammalian subject is about 2000 Hz, the accurate control should lead to such modulated low energy emission being generated at a frequency of between about 1999 and about 2001 Hz. However, and in terms of what has been determined from experiences in treating human subjects harbouring cancerous cells with the aim of arresting proliferation or killing of such cells, it is preferable that the accurate control should lead to a resolution of about 0.5, more preferably about 0.1, yet more preferably about 0.01 and indeed most preferably about 0.001 Hz of the intended determined or predetermined modulation frequency.
  • Of importance is the requirement for emissions to be at a very low and safe energy level and result in low levels of absorption, the reason believed to be that physiological exchanges or flow of electrical impulses within warm-blooded animals (which are to be affected by application of the emissions of the present invention) are similarly at very low energy levels. In any event, in the region (at or near to the position of contact or close-by induction of the electrically conductive applicator with a subject receiving treatment), the specific absorption rate (SAR) should be and is most preferably substantially less than 1.6 milliW/g weight of living tissue.
  • Furthermore of importance to achieve the intended biological therapeutic effect is that the stability of the emissions be maintained during emission, and that such stability should preferably be of the order of 10−5, more preferably 10−6, and most preferably 10−7, stability being determined as the relative deviation of frequency divided by the desired frequency, e.g. 0.01 Hz (deviation)/1,000 Hz (desired freq.)=10−5.
  • As already described in said EP 0 592 851 B1, the system includes a microprocessor (which may more recently be replaced by an integrated circuit) into which control information is loaded from an application storage device. The microprocessor (or now alternatively integrated circuit) then controls the function of the system to produce the desired therapeutic emissions. Also described is the provision in the system of an impedance transformer connected intermediate the emitter of low energy electromagnetic emissions and a probe (here more broadly described as an electrically conductive applicator) for applying the emissions to the patient. The impedance transformer substantially matches the impedance of the patient seen from the emitter circuit with the impedance of the output of the emitter circuit.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 shows an exemplary casing structure for the electronic circuit shown in FIG. 2, an applicator 13 (exemplified as a probe suitable for being placed in the mouth of a patient) and an interface 16 (which may be replaced by a receiver) for receiving information from a source of information 52 such as may be comprised in an information storage device, e.g. of the nature described and illustrated in FIGS. 12 to 17 of EP 0 592 851 B1.
  • FIG. 2 is a block diagram of exemplary circuitry which may be comprised in the exemplary casing structure of FIG. 1. This FIG. 2 differs essentially from FIG. 2 of EP 0 592 851 B1 by comprising a highly accurate modulation frequency generator 31 (named a Digital Direct Synthesizer or DDS), which enables accurate control of modulatable oscillator represented by dotted line block 106.
  • Reference is made to the various Figures of EP 0 592 851 B1 and the detailed description thereof, a number of which are exemplary of components which may be comprised in the circuit of FIG. 2.
  • Thus, FIG. 3 of EP 0 592 851 B1 is a detailed schematic of a modulation signal generator 31, replaced by a DDS modulation frequency generator 31 comprised in the circuit of present FIG. 2;
  • FIG. 4 of EP 0 592 851 B1 is a detailed schematic of a modulation signal buffer and carrier oscillator circuit which may be employed in the circuit of the present FIG. 2;
  • FIG. 5 of EP 0 592 851 B1 is a detailed schematic example of an amplitude modulation (AM) and power generator 34 and output filter 39 which could be comprised in the circuit of the present FIG. 2;
  • FIG. 6 of EP 0 592 851 B1 is a detailed schematic example of an impedance transformer 14 which may be comprised in the circuit of the present FIG. 2;
  • FIG. 7 of EP 0 592 851 B1 is a detailed schematic example of an emission sensor 53 which may be comprised in the circuit of the present FIG. 2;
  • FIG. 8 of EP 0 592 851 B1 is a detailed schematic example of an output power sensor circuit 54 which may be employed in the circuit of the present FIG. 2.
  • FIG. 9 of EP 0 592 851 B1 is a detailed schematic example of a display module or information output 17 which may be included in the circuit of the present FIG. 2.
  • FIG. 10 of EP 0 592 851 B1 is a detailed schematic example of a power supply control circuit including battery charger 57 which may be comprised in the circuit of the present FIG. 2.
  • FIGS. 11a-d of EP 0 592 851 B1 are exemplary flow charts of the method of operation of the system of FIGS. 1 and 2.
  • DETAILED DESCRIPTION
  • Referring to FIG. 1, presented is a modulated low energy electromagnetic emission application system 11, in accordance with the present invention. As described in prior U.S. Pat. Nos. 4,649,935 and 4,765,322, such a system has proven to be useful in the practice of Low Energy Emission Therapy (LEET, a trademark of Symtonic S.A. or a successor of this Company), which involves application of emissions of low energy radio frequency (RF) electromagnetic waves to a warm-blooded mammalian subject. The application has proven to be an effective mode of treating a warm-blooded mammalian subject suffering from central nervous system (CNS) disorders such as, for example, generalized anxiety disorders, panic disorders, sleep disorders including insomnia, psychiatric disorders such as depression, obsessive compulsive disorders, disorders resulting from substance abuse, sociopathy, post traumatic stress disorders or other disorders of the central nervous system and combinations thereof.
  • The system includes an electrically conductive applicator 12, 13 for applying one or more electromagnetic emissions to the warm-blooded mammalian subject. One form of applicator may consist of an electrically conductive probe or mouthpiece 13 which is inserted into the mouth of a subject undergoing treatment. Probe 13 is connected to an electromagnetic energy emitter (see also FIG. 2), through coaxial cable 12 and impedance matching transformer 14.
  • It has previously been considered that an efficient connection of an electrically conductive applicator to a subject could only be achieved by means of a probe which is adapted to be applied to any mucosa of the subject, such as by being located within oral, nasal, optical, urethral, anal, and/or vaginal cavities or surfaces. It has however now been determined that in fact satisfactory application of emissions to a patient can be achieved by simpler physical contact of the electrically conductive applicator with the skin of the patient. Emissions to the patient may, for example be achieved by a conductive, inductive, capacitive or radiated coupling to the patient. An example of a coupling found to be effective involving indirect physical contact with the skin of a patient, is an insulated applicator to be placed over or within an ear of the patient. The emissions thus passed to the patient may be either by capacitive or radiated means or by a combination of both. An important advantage of a device which does not need to be placed in the mouth of a patient is that the patient is able to speak clearly during a time of treatment and can receive treatment during activities of daily living. The treatment is accordingly more user-friendly, can be administered for longer periods of time and can lead to enhanced patient compliance.
  • Electronic system 11 also includes a connector or coupler for connection to a programmable device such as a computer or an interface or receiver 16 which is adapted to receive an application storage device 52 such as, for example, magnetic media, semiconductor media, optical media or mechanically encoded media, or programmed emissions programmed with control information employed to control the operation of system 11 so that the desired type of low energy emission therapy is applied to the patient.
  • Application storage device 52 can be provided with a microprocessor which, when applied to interface 16, operates to control the function of system 11 to apply the desired low energy emission therapy. Alternatively, application storage device 52 can be provided with a microprocessor which is used in combination with microprocessor 21 within system 11. In such case, the microprocessor within device 52 could assist in the interfacing of storage device 52 with system 11, or could provide security checking functions.
  • System 11 may also include a display 17 which can display various indications of the operation of system 11. In addition, system 11 may include on and off power buttons 18 and 19, optionally replaced by user interface 21A (refer to FIG. 2).
  • Referring to FIG. 2, presented is a block diagram of exemplary electronic circuitry of system 11, in accordance with the present invention. A data processor, such as for example, microprocessor or integrated circuit 21, operates as the controller for electronic system 11, and is connected to control the various components of the system 11, for example, through address bus 22, data bus 23 and input/output lines 25. The block diagram of FIG. 2 is modified as compared to FIG. 2 of EP 0 592 851 B1 by including what is known as a digital direct synthesizer (DDS) 31 which operates as a accurate and stable modulation frequency generator within the system 11. An exemplary DDS device is available from Analog Devices of Norwood, Mass. 02062-9106, USA, Part No AD9835. The device is a numerically controlled oscillator and modulation capabilities are provided for phase modulation and frequency modulation. As represented by dotted line block 102, entitled “PROCESSOR WITH DAC”, the functionality of the DDS may also be combined with microprocessor 21 with digital to analogue converter (DAC).
  • Microprocessor 21 preferably includes internal storage for the operation of a coded control program, and temporary data. In addition, microprocessor 21 may include input/output ports and internal timers. Microprocessor 21 may be a microcontroller, for example microcontrollers 8048 or 8051 available from Intel Corporation of Santa Clara, Calif. 95054-1549, USA.
  • The timing for microprocessor 21 is provided by system clock oscillator 26A which may be run at any clock frequency suitable for the particular type of microprocessor used. An exemplary clock frequency is about 8.0 MHz. Oscillator 26A may be replaced by reference frequency oscillator 26 which secures the stability of the accurate modulation frequency. RF (radio frequency) oscillator 32 may also be employed for this purpose. A combination of oscillators is represented by dotted line block 104, entitled “OSCILLATOR”.
  • An exemplary operating program for microprocessor 21 is presented in flow chart form with reference to FIGS. 11a-d of EP 0 592 851 B1. In general, microprocessor 21 functions to control controllable electromagnetic energy generator circuit 29 to produce a desired form of modulated low energy electromagnetic emission for application to a subject through applicator or probe 13.
  • Dotted line block 29, entitled CONTROLLABLE GENERATOR, includes DDS modulation frequency generator 31 and carrier signal oscillator 32. Microprocessor 21 operates to activate or deactivate controllable generator circuit 29 through oscillator disable line 33, as described in greater detail in EP 0 592 851 B1. Controllable generator circuit 29 also includes an AM modulator and power generator 34 which operates to amplitude modulate a carrier signal produced by carrier oscillator 32 on carrier signal line 36, with a modulation signal produced by modulation signal generator circuit 31 on modulation signal line 37. The combination of the functionality of the DDS modulation frequency generator 31, with processor 21 with DAC, represented by dotted line block 102, enables output lines 33 and 37 to be combined to produce a single signal. The combination furthermore enables arbitrary or periodic wave forms of any shape to be generated, as similarly described in EP 0 592 851 B1.
  • AM modulator and power generator 34 produces an amplitude modulated carrier signal on modulated carrier signal line 38, which is then applied to emitter output filter circuit 39. The filter circuit 39 is connected to probe or applicator 13 via power emission sensor 54, coaxial cable 12 and impedance transformer 14.
  • Microprocessor 21 controls DDS modulation signal generator circuit 31 of controllable generator circuit 29 via interface lines 25.
  • As is illustrated and described in EU 0 592 851 B1, microprocessor 21 may select a desired waveform stored in a modulation waveform storage device 43 and also controls a waveform address generator 41 to produce on waveform address bus 42 a sequence of addresses which are applied to modulation signal storage device 43 in order to retrieve the selected modulation signal. In the embodiment described in EP 0 592 851 B1, the desired modulation signal is retrieved from modulation signal storage device 43 and applied to modulation signal bus 44 in digital form. Modulation signal bus 44 is applied to wave form generator and DAC 46 which converts the digital modulation signal into analogue form. This analogue modulation signal is then applied to a selective filter 47 which, under control of microprocessor 21, filters the analogue modulation signal by use of a variable filter network including resistor 48 and capacitors 49 and 51 in order to smooth the wave form produced by DAC 46 on modulation signal line 20.
  • A further embodiment possibility is a combination of PROCESSOR WITH DAC dotted line block 102 with OSCILLATOR dotted line block 104 or with a combination of oscillators 26 and 26A. With such a combination, the hardware solution described in EP 0 592 851 B1 can be realized internally in the processor 102 with multiple outputs 33 and 37 or a single output combining these signals.
  • The above embodiment from EP 0 592 851 B1 is in part replaced by the functionality of the DDS modulation frequency modulator 31. However, if it is determined that emissions of different wave forms is desirable, it would be desirable to include the modulation signal storage device 43 and wave form generator 46 described in EP 0 592 851 B1. Various modulation signal wave forms may then be stored in modulation signal storage device 43. Wave forms that have been successfully employed include square wave forms or sinusoidal wave forms. Other possible modulation signal wave forms include rectified sinusoidal, triangular, or other wave forms and combinations of all of the above.
  • The particular modulation control information employed by microprocessor 21 to control the operation of controllable generator circuit 29, is stored in application storage device 52. The application storage device is conveniently a computer comprising or being for receiving the information. Alternatively, application storage devices illustrated and described in EP 0 592 851 B1, with reference to FIGS. 12, 13, 14 and 15, may be selected.
  • Interface 16 is configured as appropriate for the particular application storage device 52 in use. Interface 16 translates the control information stored in application storage device 52 into a usable form for storage within the memory of microprocessor 21 to enable microprocessor 21 to control controllable generator circuit 29 to produce the desired modulated low energy emission.
  • Interface 16 may directly read the information stored on application storage device 52, or it may read the information through use of various known communication links. For example, radio frequency, microwave, laser, telephone, internet or optical based communications links may be employed to transfer information between interface or receiver 16 and application storage device or computer 52.
  • The system 11 may comprise a user identification device, included in block 21 a in FIG. 2. Conveniently, such a device communicates with the one or more data processors or integrated circuits 21 via interface 16, as shown. The user identification device may be of any type, a finger print reader being an example. Such a reader is for example available from Lenovo, 70563 Stuttgart, Germany, Part No. 73P4774.
  • The control information stored in application storage device or computer 52 specifies various controllable parameters of the modulated low energy RF electromagnetic emission to be applied to a subject through applicator or probe 13. Such controllable parameters include, for example, but are not necessarily limited to, the frequency and amplitude of the carrier, the amplitudes and frequencies and wave forms of the modulation of the carrier, the duration of the emission, the power level of the emission, the duty cycle of the emission (i.e., the ratio of on time to off time of pulsed emissions applied during a treatment), the sequence of application of different modulation frequencies for a particular application, and the total number of treatments and duration of each treatment prescribed for a particular subject, and combinations thereof.
  • For example, the carrier signal and modulation signal may be selected to drive the applicator or probe 13 with an amplitude modulated signal in which the carrier signal includes spectral frequency components below about 1 GHz, and preferably between about 1 MHz and about 900 MHz, and in which the modulation signal comprises spectral frequency components between about 0.01 Hz and 150 KHz. The one or more modulation frequencies may be simultaneously emitted or sequenced to form the modulation signal.
  • As an additional feature, an electromagnetic emission sensor 53 may be provided to detect the presence of electromagnetic emissions at the frequency of the carrier oscillator 32. Emission sensor 53 provides microprocessor 21 with an indication of whether or not electromagnetic emissions at the desired frequency are present. Microprocessor 21 then takes appropriate action, for example, by displaying an error message on display 17, disabling controllable generator circuit 29, or the like.
  • A power sensor 54 is preferably included which detects the amount of power applied to the subject through applicator or probe 13 compared to the amount of power returned or reflected from the subject. This ratio is indicative of the proper use of the system during a therapeutic session. Power sensor 54 applies to microprocessor 21, through power sensor line 56, an indication of the amount of power applied to patient through applicator or probe 13 relative to the amount of power reflected from the patient.
  • The indication provided on power sense line 56 may be digitalized and employed by microprocessor 21, for example, to detect and control a level of applied power, and to record on application storage device 52 information related to the actual treatments applied to and received by the patient. Such information may then be used by a physician or other clinician to assess patient treatment compliance and effect. Such treatment information may include, for example: the number of treatments applied for a given time period; the actual time and date of each treatment; the number of attempted treatments; the treatment compliance (i.e., whether the applicator or probe was in place or not during the treatment session); and the cumulative dose of a particular modulation frequency.
  • The level of power applied is preferably controlled to cause the specific absorption rate (SAR) of energy absorbed by the patient to be from about 1 microWatt per kilogram of tissue to about 50 Watts per kilogram of tissue. Preferably, the power level is controlled to cause an SAR of from about 100 microWatts per kilogram of tissue to about 10 Watts per kilogram of tissue. Most preferably, the power level is controlled to cause an SAR of from about 1 milliWatt per kilogram of tissue to about 100 milliWatts per kilogram of tissue. These SARs may be in any tissue of the patient, but are preferably in the tissue of the central nervous system or the diseased tissue.
  • System 11 may also include powering circuitry including battery and charger circuit 57 and battery voltage change detector 58.
  • The RF carrier oscillator 32 produces a RF carrier frequency of about 27 MHz. Other embodiments of the invention contemplate RF carrier frequencies of about 48 MHz, about 433 MHz or about 900 MHz. In general, the RF carrier frequency produced by carrier oscillator 32 has spectral frequency components less than about 1 GHz and preferably between about 1 MHz and about 916 MHz. Although the described embodiment contemplates that once set, the carrier oscillator frequency remains substantially constant, the carrier frequency produced by carrier oscillator 32 may be variable and controllable by microprocessor 21 by use of stored or transmitted control information.
  • Carrier oscillator 32 produces on carrier signal line 36 a carrier signal which is then modulated by the modulation signal carried on signal line 37.
  • Oscillator disable line 33 enables microprocessor 21 to disable the signal from oscillator 32 by applying an appropriate disable signal to oscillator disable line 33.
  • The output of the AM modulator and power generator 34 appears on signal line 38. This modulated signal is applied through emitter output filter 39 which substantially reduces or eliminates the carrier harmonics resulting from side effects of the modulator and power generator circuit 34.
  • The output of the AM modulator and power generator 34 and emitter output filter 39 may be designed to possess a 50 Ohm output impedance to match a 50 Ohm impedance of coaxial cable 12.
  • It has been determined through impedance measurements that when a probe 13 is applied within the mouth of a subject, the probe/subject combination exhibits a complex impedance of the order of about 150+j200 Ohms. Impedance transformer 14 serves to match this complex impedance with the 50 Ohm impedance of coaxial cable 12 and therefore the output impedance of the AM modulator 34 and output filter 39. This promotes power transmission, and minimizes reflections.
  • The arrangement described above has been optimized for a contact probe with coupling to the mucosa of the mouth. In a further example, a conductive, isolated probe has been used at a frequency around 433 MHz coupling to the outer ear channel. Due to the different probe design in such a frequency band and with this coupling method, the values of matching elements (79 and 81 described in EP 0592 851 B1) would be different or could even be omitted. Applicator or probe 13 may then be regarded as a capacitive coupler or as an antenna matched to the capacitive load.
  • As described in EP 0 592 851 B1, with reference to the flow charts of FIGS. 11a-d, microprocessor 21 may operate to analyse the signal appearing on power sense line 56 to determine and control the amount of power applied to the patient, and to assess patient treatment compliance, and possibly to record indicia of the patient treatment compliance on application storage device 52 for later analysis and assessment by a physician or other clinician.
  • Exemplary of treatments performed on patients have included brain, bladder, colorectal, kidney, mesothelium, neuroendocrine, liver, lung, breast, ovary, pancreas, prostate and thyroid tumour types. The treatments involved applying an about 27.12 MHz RF signal, amplitude modulated at specifically defined frequencies ranging from about 0.2 to about 23,000 Hz at very high precision and stability. Further Examples of treatment modes (at specific accurately controlled AM frequencies) for specified types of tumours are described in detail below.
  • The following are synopses of abstracts for future publications related to uses of electronic devices of the present invention:
  • A Example A A Phase I Study of Therapeutic Amplitude-Modulated Electromagnetic Fields (THERABIONIC) in Advanced Tumors
  • Boris Pasche 1, Alexandre Barbault 1, Brad Bottger 2, Fin Bomholt 3, Niels Kuster 4. 1 Cabinet Médical de l'Avenue de la Gare 6, CH-1003-Lausanne, Switzerland.2 Danbury Hospital, Danbury, Conn.-06810.3 SPEAG, Zurich, CH-8004-Zurich, Switzerland4 IT'IS Foundation, Swiss Federal Institute of Technology, Zurich, Switzerland.
  • Background: In vitro studies suggest that low levels of amplitude-modulated electromagnetic fields may modify cell growth. Specific frequencies have been identified specific frequencies that may block cancer cell growth. A portable and programmable device capable of delivering low levels of amplitude-modulated electromagnetic fields has been developed. The device emits a 27.12 MHz radiofrequency signal, amplitude-modulated at cancer-specific frequencies ranging from 0.2 to 23,000 Hz with high precision. The device is connected to a spoon-like coupler, which is placed in the patient's mouth during treatment.
  • Methods: A phase I study was conducted consisting of three daily 40 min treatments. From March 2004 to September 2006, 24 patients with advanced solid tumors were enrolled. The median age was 57.0±12.2 years. 16 patients were female. As of January 2007, 5 patients are still on therapy, 13 patients died of tumor progression, 2 patients are lost to follow-up and one patient withdrew consent. The most common tumor types were breast (7), ovary (5) and pancreas (3). 22 patients had received prior systemic therapy and 16 had documented tumor progression prior to study entry.
  • Results: The median duration of therapy was 15.7±19.9 weeks (range: 0.4-72.0 weeks). There were no NCI grade 2, 3 or 4 toxicities. Three patients experienced grade 1 fatigue during and immediately after treatment. 12 patients reported severe pain prior to study entry. Two of them reported significant pain relief with the treatment. Objective response could be assessed in 13 patients, 6 of whom also had elevated tumor markers. 6 additional patients could only be assessed by tumor markers. Among patients with progressive disease at study entry, one had a partial response for >14.4 weeks associated with >50% decrease in CEA, CA 125 and CA 15-3 (previously untreated metastatic breast cancer); one patient had stable disease for 34.6 weeks (add info); one patient had a 50% decrease in CA 19-9 for 12.4 weeks (recurrent pancreatic cancer). Among patients with stable disease at enrollment, four patients maintained stable disease for 17.0, >19.4, 30.4 and >63.4 weeks.
  • Conclusions: The treatment is a safe and promising novel treatment modality for advanced cancer. A phase II study and molecular studies are ongoing to confirm those results.
  • Example B A Phase II Study of Therapeutic Amplitude-Modulated Electromagnetic Fields (THERABIONIC) in the Treatment of Advanced Hepatocellular Carcinoma (HCC)
  • Frederico P Costa 1, Andre Cosme de Oliveira 1, Roberto Meirelles Jr 1, Rodrigo Surjan 1, Tatiana Zanesco 1, Maria Cristina Chammas 1, Alexandre Barbault 2, Boris Pasche 2. 1 Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil. 2Cabinet Médical Avenue de la Gare 6, CH-1003-Lausanne, Switzerland
  • Background: Phase I data suggest that low levels of electromagnetic fields amplitude-modulated at specific frequencies administered intrabucally with the device of Example A are a safe and potentially effective treatment for advanced cancer. The device emits a 27.12 MHz RF signal, amplitude-modulated with cancer-specific frequencies ranging from 0.2 to 23,000 Hz with high precision. The device is connected to a spoon-like coupler placed in the patient's mouth during treatment. Patients with advanced hepatocellular carcinoma HCC and limited therapeutic options were offered treatment with a combination of HCC-specific frequencies.
  • Methods: From October 2005 to October 2006, 38 patients with advanced HCC were recruited in a phase II study. The patients received three daily 40 min treatments until disease progression or death. The median age was 64.0±14.2 years. 32 patients were male and 29 patients had documented progression of disease (POD) prior to study entry.
  • Results: As of January 2007, 12 patients are still on therapy, 20 patients died of tumor progression, 2 patients are lost to follow-up and 3 patients withdrew consent. 27 patients are eligible for response. The overall objective response rate as defined by partial response (PR) or stable disease (SD) in patients with documented POD at study entry was 31.6%: 3 PR and 9 SD. The median survival was 20.7 weeks with a median duration of therapy of 17.5 weeks. 13 patients have received therapy for more than six months. The median duration of response is 12.9 weeks. 12 patients reported pain at study entry: 8 of them (66%) experienced decreased pain during treatment. There were no NCI grade 2/3/4 toxicities. One patient developed grade 1 mucositis and grade 1 fatigue.
  • Patient characteristics (n = 38)
    Cirrhosis 36
    Portal vein thrombosis 9
    Elevated AFP 25
    Extra-hepatic metastases 12
    Previous intrahepatic/systemic therapy 30
    Previous hepatic resection/RFA or 8
    ethanol
    CLIP 0/1: 12 >2: 22
    Okuda I: 14 II/III: 20
    Child-Pugh A: 15 B: 19
    MELD Median: 10
  • Conclusion: In patients with advanced HCC the treatment is a safe and effective novel therapeutic option, which has antitumor effect and provides pain relief in the majority of patients.
  • Thus, it is seen that the electronic device of the present invention, comprising means for the accurate control over the frequencies and stability of amplitude modulations of a high frequency carrier signal, provides a safe and promising novel treatment modality for the treatment of patients suffering from various types of advanced forms of cancer.
  • Exemplary of above accurately controlled amplitude modulated frequencies controlling the frequency of amplitude modulations of a high frequency carrier signal are set forth below along with the type of cancer or tumour harboured by a subject to be treated.
  • Example 1 AM Frequencies Employed for Treatment of Breast Cancer (188 Frequencies so Far Included)
  •   78.76 Hz
     181.821 Hz
     414.817 Hz
     440.933 Hz
     628.431 Hz
     721.313 Hz
     813.205 Hz
     818.342 Hz
     891.901 Hz
     929.095 Hz
      929.1 Hz
       1021 Hz
    1372.207 Hz
    1372.934 Hz
    1588.721 Hz
    1670.699 Hz
    1821.729 Hz
    1836.219 Hz
    2193.937 Hz
    2221.323 Hz
    2278.312 Hz
    2357.832 Hz
    2381.443 Hz
    2417.323 Hz
    2431.334 Hz
    2450.332 Hz
    2551.313 Hz
    2556.221 Hz
    2598.853 Hz
    2621.322 Hz
    2740.191 Hz
    2851.347 Hz
    2885.322 Hz
    2919.273 Hz
    3074.333 Hz
    3115.188 Hz
    3249.529 Hz
    3405.182 Hz
    3432.274 Hz
    3434.693 Hz
    3594.231 Hz
    3647.619 Hz
    3742.957 Hz
    3753.382 Hz
    3830.732 Hz
    3855.823 Hz
    3916.321 Hz
    3935.218 Hz
    3975.383 Hz
    3993.437 Hz
    4153.192 Hz
    4194.968 Hz
    4241.321 Hz
    4243.393 Hz
    4253.432 Hz
    4314.444 Hz
    4318.222 Hz
    4375.962 Hz
    4393.419 Hz
    4417.243 Hz
    4481.463 Hz
    4482.223 Hz
    4495.138 Hz
    4549.808 Hz
    4558.306 Hz
    4779.451 Hz
    4838.674 Hz
    4871.513 Hz
    4895.296 Hz
    4962.213 Hz
    4969.224 Hz
    4979.321 Hz
    5027.231 Hz
    5059.792 Hz
    5118.094 Hz
    5176.287 Hz
    5365.222 Hz
    5376.392 Hz
    5426.323 Hz
    5431.542 Hz
    5521.621 Hz
    5739.422 Hz
    5745.218 Hz
    5821.975 Hz
    6037.432 Hz
    6044.333 Hz
    6086.256 Hz
    6208.932 Hz
    6212.808 Hz
    6231.031 Hz
    6280.321 Hz
    6329.391 Hz
    6476.896 Hz
    6497.319 Hz
    6504.983 Hz
    6651.276 Hz
    6757.901 Hz
    6758.321 Hz
    6855.286 Hz
    6858.121 Hz
    6898.489 Hz
    7092.219 Hz
    7120.218 Hz
    7127.311 Hz
    7156.489 Hz
    7208.821 Hz
    7282.169 Hz
    7376.329 Hz
    7488.742 Hz
    7541.319 Hz
    7577.421 Hz
    7621.085 Hz
    7627.207 Hz
    7650.939 Hz
    7691.212 Hz
    7842.184 Hz
    7849.231 Hz
    7915.423 Hz
    7932.482 Hz
    7949.196 Hz
    7967.311 Hz
    8021.229 Hz
    8070.181 Hz
    8114.032 Hz
    8149.922 Hz
     8194.19 Hz
    8245.801 Hz
    8328.322 Hz
    8330.534 Hz
    8355.987 Hz
    8408.121 Hz
    8431.184 Hz
    8452.119 Hz
    8548.324 Hz
    8749.383 Hz
    8782.421 Hz
    8784.424 Hz
     8923.1 Hz
    8923.361 Hz
    8935.752 Hz
     8936.1 Hz
    9012.282 Hz
    9012.896 Hz
    9060.323 Hz
    9072.409 Hz
    9131.419 Hz
    9199.232 Hz
    9245.927 Hz
    9270.322 Hz
    9279.193 Hz
    9393.946 Hz
    10227.242 Hz 
    10340.509 Hz 
    10363.313 Hz 
    10449.323 Hz 
    10456.383 Hz 
    10468.231 Hz 
    10470.456 Hz 
    10472.291 Hz 
    10689.339 Hz 
    10832.222 Hz 
    11525.121 Hz 
    11541.915 Hz 
    11812.328 Hz 
    11812.419 Hz 
    11840.323 Hz 
    11925.089 Hz 
    12123.281 Hz 
    12267.281 Hz 
    12294.283 Hz 
    12611.288 Hz 
    12629.222 Hz 
    12633.372 Hz 
    12648.221 Hz 
    13315.335 Hz 
    13331.358 Hz 
    13735.241 Hz 
    13826.325 Hz 
    13853.232 Hz 
    13990.123 Hz 
    14122.942 Hz 
    14162.332 Hz 
    14519.232 Hz 
    14543.128 Hz 
    15651.323 Hz 
    17352.085 Hz 
    18785.463 Hz 
    30182.932 Hz 
  • Example 2 AM Frequencies Employed for Treatment of Liver Cancer (162 Frequencies so Far Included)
  •  423.321 Hz
     427.062 Hz
     470.181 Hz
     560.32 Hz
     642.932 Hz
     668.209 Hz
     677.972 Hz
     811.924 Hz
     842.311 Hz
     843.22 Hz
    1250.504 Hz
    1755.402 Hz
    1873.477 Hz
    1924.702 Hz
    1975.196 Hz
    2017.962 Hz
    2083.419 Hz
    2190.731 Hz
    2221.323 Hz
    2324.393 Hz
    2353.478 Hz
    2362.309 Hz
    2419.309 Hz
    2425.222 Hz
    2430.219 Hz
    2431.094 Hz
    2471.328 Hz
    2478.331 Hz
    2743.995 Hz
    2744.211 Hz
    2831.951 Hz
    2843.283 Hz
    2859.891 Hz
    2873.542 Hz
    2886.232 Hz
    3042.012 Hz
    3078.983 Hz
    3086.443 Hz
    3127.232 Hz
    3160.942 Hz
    3206.315 Hz
    3267.433 Hz
    3269.321 Hz
    3457.291 Hz
    3505.229 Hz
    3516.296 Hz
    3531.296 Hz
    3546.323 Hz
    3572.106 Hz
    3576.189 Hz
    3669.513 Hz
    3923.221 Hz
    4013.932 Hz
    4071.121 Hz
    4079.951 Hz
    4222.821 Hz
    4238.402 Hz
    4256.321 Hz
    4289.296 Hz
    4312.947 Hz
    4435.219 Hz
    4471.188 Hz
    4483.889 Hz
    4486.384 Hz
    4629.941 Hz
    4732.211 Hz
    4876.218 Hz
    5086.281 Hz
    5124.084 Hz
    5133.121 Hz
    5247.142 Hz
    5270.834 Hz
    5340.497 Hz
    5520.218 Hz
    5882.292 Hz
    5926.512 Hz
    6037.311 Hz
    6180.334 Hz
    6329.195 Hz
    6350.333 Hz
    6361.321 Hz
    6364.928 Hz
    6383.321 Hz
    6461.175 Hz
    6733.331 Hz
    6758.232 Hz
    6779.482 Hz
    6856.222 Hz
    6877.183 Hz
    6980.525 Hz
    7019.235 Hz
    7043.209 Hz
    7130.323 Hz
    7144.142 Hz
    7210.223 Hz
     7291.21 Hz
     7510.92 Hz
    7529.233 Hz
    7549.212 Hz
    7650.028 Hz
    7680.518 Hz
    7692.522 Hz
    7829.231 Hz
    7862.209 Hz
    7947.392 Hz
    7979.308 Hz
    8028.339 Hz
    8055.942 Hz
    8072.134 Hz
    8141.174 Hz
    8336.383 Hz
    8432.181 Hz
    8452.119 Hz
    8460.944 Hz
    8475.221 Hz
    8492.193 Hz
    8542.311 Hz
    8818.104 Hz
    8852.329 Hz
    8853.444 Hz
    8858.179 Hz
    8939.212 Hz
    9332.397 Hz
    9381.221 Hz
    9740.219 Hz
    9768.331 Hz
    9797.294 Hz
    10317.499 Hz 
    10443.311 Hz 
    10456.383 Hz 
    10579.425 Hz 
    10863.209 Hz 
    10866.382 Hz 
    11067.418 Hz 
    11149.935 Hz 
    11163.895 Hz 
    11802.821 Hz 
    11953.424 Hz 
    12223.329 Hz 
    12265.295 Hz 
    12267.233 Hz 
    12623.191 Hz 
    12685.231 Hz 
    12721.423 Hz 
    12785.342 Hz 
    14085.222 Hz 
    14333.209 Hz 
    14537.331 Hz 
    14542.432 Hz 
    14655.03 Hz
    14828.234 Hz 
    15149.213 Hz 
    15237.489 Hz 
    16110.932 Hz 
    16144.343 Hz 
    18265.238 Hz 
    18283.323 Hz 
    18863.292 Hz 
    18930.995 Hz 
    19970.311 Hz 
    20330.294 Hz 
    20365.284 Hz 
  • Example 3 AM Frequencies Employed for Treatment of Ovarian Cancer (273 Frequencies so Far Included)
  • 78.76 Hz
    181.821 Hz
    410.245 Hz
    414.817 Hz
    436.332 Hz
    447.942 Hz
    481.191 Hz
    489.292 Hz
    559.292 Hz
    608.321 Hz
    655.435 Hz
    657.397 Hz
    657.483 Hz
    664.211 Hz
    708.8 Hz
    708.822 Hz
    734.921 Hz
    749.221 Hz
    764.232 Hz
    778.295 Hz
    779.403 Hz
    806.021 Hz
    806.389 Hz
    809.313 Hz
    824.327 Hz
    825.145 Hz
    835.129 Hz
    839.521 Hz
    841.208 Hz
    843.312 Hz
    956.984 Hz
    958.929 Hz
    985.313 Hz
    1024.208 Hz
    1102.635 Hz
    1121.329 Hz
    1159.738 Hz
    1372.207 Hz
    1396.498 Hz
    1502.181 Hz
    1518.208 Hz
    1552.123 Hz
    1579.212 Hz
    1624.802 Hz
    1670.699 Hz
    1696.403 Hz
    1762.938 Hz
    1771.402 Hz
    1775.313 Hz
    1821.729 Hz
    2016.323 Hz
    2034.231 Hz
    2050.282 Hz
    2053.396 Hz
    2082.234 Hz
    2089.092 Hz
    2221.323 Hz
    2228.832 Hz
    2253.704 Hz
    2254.329 Hz
    2278.312 Hz
    2332.949 Hz
    2348.233 Hz
    2381.443 Hz
    2413.193 Hz
    2425.222 Hz
    2433.321 Hz
    2439.253 Hz
    2465.23 Hz
    2477.919 Hz
    2669.177 Hz
    2715.232 Hz
    2733.843 Hz
    2802.339 Hz
    2812.321 Hz
    2831.386 Hz
    2835.332 Hz
    2851.347 Hz
    2877.192 Hz
    2885.322 Hz
    2887.385 Hz
    2894.972 Hz
    2973.771 Hz
    3080.592 Hz
    3157.483 Hz
    3161.465 Hz
    3223.232 Hz
    3238.148 Hz
    3249.529 Hz
    3262.145 Hz
    3314.321 Hz
    3361.671 Hz
    3366.311 Hz
    3523.215 Hz
    3527.233 Hz
    3542.213 Hz
    3590.376 Hz
    3629.232 Hz
    3632.793 Hz
    3636.289 Hz
    3637.085 Hz
    3669.513 Hz
    3770.189 Hz
    3858.916 Hz
    3919.232 Hz
    3957.185 Hz
    3975.228 Hz
    4061.131 Hz
    4072.322 Hz
    4169.451 Hz
    4174.259 Hz
    4241.321 Hz
    4243.393 Hz
    4261.228 Hz
    4279.113 Hz
    4309.335 Hz
    4314.188 Hz
    4318.222 Hz
    4328.928 Hz
    4380.321 Hz
    4394.134 Hz
    4412.252 Hz
    4424.236 Hz
    4439.341 Hz
    4442.161 Hz
    4447.221 Hz
    4458.339 Hz
    4556.322 Hz
    4566.009 Hz
    4682.643 Hz
    4718.331 Hz
    4749.302 Hz
    4765.331 Hz
    4917.202 Hz
    5011.325 Hz
    5149.331 Hz
    5228.172 Hz
    5237.132 Hz
    5313.353 Hz
    5745.218 Hz
    5757.897 Hz
    5762.386 Hz
    5812.322 Hz
    5869.321 Hz
    5882.292 Hz
    5921.249 Hz
    5991.932 Hz
    6069.458 Hz
    6071.319 Hz
    6083.214 Hz
    6161.782 Hz
    6169.341 Hz
    6275.232 Hz
    6294.929 Hz
    6350.333 Hz
    6406.891 Hz
    6407.207 Hz
    6450.787 Hz
    6477.098 Hz
    6477.929 Hz
    6478.338 Hz
    6543.421 Hz
    6552.24 Hz
    6663.955 Hz
    6753.338 Hz
    6851.323 Hz
    6855.286 Hz
    6875.232 Hz
    6882.949 Hz
    7206.403 Hz
    7232.214 Hz
    7257.489 Hz
    7276.209 Hz
    7281.219 Hz
    7285.693 Hz
    7429.212 Hz
    7460.932 Hz
    7480.228 Hz
    7495.763 Hz
    7539.432 Hz
    7564.185 Hz
    7650.028 Hz
    7689.728 Hz
    7780.294 Hz
    8021.921 Hz
    8038.961 Hz
    8040.322 Hz
    8044.233 Hz
    8095.313 Hz
    8143.491 Hz
    8164.332 Hz
    8261.121 Hz
    8302.285 Hz
    8309.752 Hz
    8372.532 Hz
    8408.121 Hz
    8424.229 Hz
    8428.313 Hz
    8435.451 Hz
    8486.421 Hz
    8492.797 Hz
    8548.324 Hz
    8554.361 Hz
    8562.965 Hz
    8579.323 Hz
    8579.333 Hz
    8642.181 Hz
    8655.818 Hz
    8758.341 Hz
    8779.323 Hz
    8792.231 Hz
    8819.127 Hz
    8831.132 Hz
    9028.031 Hz
    9173.264 Hz
    9184.338 Hz
    9186.919 Hz
    9393.946 Hz
    9482.409 Hz
    9737.211 Hz
    9746.232 Hz
    9922.231 Hz
    10032.684 Hz
    10446.028 Hz
    10478.221 Hz
    10545.313 Hz
    10639.345 Hz
    10743.118 Hz
    10813.981 Hz
    10832.421 Hz
    10838.243 Hz
    10862.429 Hz
    10865.127 Hz
    10917.229 Hz
    10977.188 Hz
    11120.209 Hz
    11177.289 Hz
    11177.409 Hz
    11321.491 Hz
    11359.093 Hz
    11673.031 Hz
    11793.886 Hz
    11895.229 Hz
    12074.531 Hz
    12216.212 Hz
    12253.329 Hz
    12260.933 Hz
    12262.853 Hz
    12292.222 Hz
    12357.353 Hz
    12527.032 Hz
    12755.333 Hz
    12947.311 Hz
    13717.221 Hz
    13825.295 Hz
    13829.195 Hz
    14410.949 Hz
    14436.201 Hz
    14537.218 Hz
    14947.184 Hz
    15429.139 Hz
    15443.309 Hz
    15450.183 Hz
    16144.343 Hz
    17932.432 Hz
    17951.395 Hz
    17970.122 Hz
    18337.222 Hz
    18378.321 Hz
    18921.415 Hz
    18926.951 Hz
    18931.327 Hz
    114508.332 Hz
  • Example 4 AM Frequencies Employed for Treatment of Prostate Cancer (183 Frequencies so Far Included)
  •   331.3 Hz
     331.358 Hz
     403.218 Hz
     461.233 Hz
      522.2 Hz
     522.213 Hz
      618.4 Hz
     618.407 Hz
      618.8 Hz
     656.295 Hz
     657.394 Hz
     657.397 Hz
      657.4 Hz
     657.483 Hz
     659.033 Hz
      694.4 Hz
     694.689 Hz
      694.7 Hz
      741.4 Hz
     741.421 Hz
     749.221 Hz
      752.9 Hz
     752.933 Hz
     776.194 Hz
     785.219 Hz
     786.332 Hz
     793.331 Hz
     809.205 Hz
     819.322 Hz
      844.8 Hz
     844.822 Hz
     847.332 Hz
    1083.309 Hz
    1102.635 Hz
     1102.71 Hz
    1240.336 Hz
    1372.934 Hz
    1444.288 Hz
    1486.322 Hz
    1563.332 Hz
    1591.322 Hz
    1670.699 Hz
    1697.321 Hz
    1743.521 Hz
    2031.448 Hz
    2050.282 Hz
    2076.519 Hz
    2156.332 Hz
    2229.515 Hz
    2243.121 Hz
    2381.443 Hz
    2440.489 Hz
    2475.912 Hz
    2477.919 Hz
    2628.324 Hz
    2669.328 Hz
    2824.832 Hz
    2887.829 Hz
    2891.331 Hz
    3081.523 Hz
    3249.529 Hz
    3250.125 Hz
    3251.815 Hz
    3264.827 Hz
    3278.329 Hz
    3281.432 Hz
    3348.783 Hz
    3519.118 Hz
    3539.962 Hz
    3551.318 Hz
    3556.439 Hz
    3572.321 Hz
    3670.129 Hz
    3681.341 Hz
    3686.021 Hz
    3753.382 Hz
    3774.923 Hz
    3867.692 Hz
    3909.333 Hz
    3916.321 Hz
    4031.233 Hz
    4031.933 Hz
    4038.203 Hz
    4081.743 Hz
    4084.319 Hz
    4139.322 Hz
    4153.192 Hz
    4223.795 Hz
    4231.221 Hz
    4241.321 Hz
    4320.513 Hz
    4329.152 Hz
    4380.321 Hz
    4417.312 Hz
    4489.452 Hz
    4549.808 Hz
    4558.306 Hz
    4638.293 Hz
    4740.322 Hz
    4854.318 Hz
    4882.322 Hz
    4978.822 Hz
    5237.152 Hz
    5264.222 Hz
    5289.195 Hz
    5426.323 Hz
    5431.542 Hz
    5455.593 Hz
    6345.332 Hz
    6347.433 Hz
    6363.284 Hz
    6418.331 Hz
    6496.231 Hz
    6538.295 Hz
    6577.421 Hz
    6590.328 Hz
    6651.276 Hz
    6706.431 Hz
    6743.322 Hz
    6783.282 Hz
    6850.197 Hz
    6855.286 Hz
    6864.896 Hz
    6871.943 Hz
    6973.393 Hz
    7120.932 Hz
    7146.509 Hz
    7192.505 Hz
    7251.309 Hz
    7251.322 Hz
    7278.124 Hz
    7279.335 Hz
    7299.119 Hz
    7527.229 Hz
    7589.925 Hz
    7699.193 Hz
    7842.184 Hz
     8023.32 Hz
    8096.939 Hz
    8245.801 Hz
    8315.291 Hz
    8357.305 Hz
    8408.121 Hz
    8432.209 Hz
    8535.238 Hz
    8552.431 Hz
    8585.224 Hz
    8935.752 Hz
    9015.253 Hz
    9018.233 Hz
    9068.231 Hz
    9137.232 Hz
    9156.321 Hz
    9351.931 Hz
    9393.946 Hz
    9694.179 Hz
    9984.405 Hz
    10226.223 Hz 
    10390.232 Hz 
    10514.768 Hz 
    10689.339 Hz 
    10772.419 Hz 
    10818.452 Hz 
    11165.239 Hz 
    11985.353 Hz 
    12209.329 Hz 
    12308.321 Hz 
    12583.339 Hz 
    13820.329 Hz 
    14013.123 Hz 
    14171.434 Hz 
    14681.329 Hz 
    14759.131 Hz 
    14986.794 Hz 
    15930.249 Hz 
    16026.623 Hz 
    17880.954 Hz 
    18247.532 Hz 
    18282.211 Hz 
    18629.328 Hz 
    19469.318 Hz 
    19766.218 Hz 
    60317.352 Hz 
  • Example 5 AM Frequencies Employed for Treatment of Kidney Cancer (36 Frequencies so Far Included)
  •  628.321 Hz
     631.141 Hz
     643.312 Hz
     812.512 Hz
     826.321 Hz
    1372.934 Hz
    2082.241 Hz
    2156.931 Hz
    2254.329 Hz
    3555.209 Hz
    3928.343 Hz
    4420.932 Hz
    4819.228 Hz
    4828.321 Hz
    5314.322 Hz
    6007.332 Hz
    7054.279 Hz
    7074.429 Hz
    7254.343 Hz
    8041.289 Hz
    8727.224 Hz
    8760.983 Hz
    8831.132 Hz
    8870.228 Hz
    10565.321 Hz 
    10586.229 Hz 
    10634.293 Hz 
    10687.949 Hz 
    11421.933 Hz 
    11523.212 Hz 
    11561.221 Hz 
    11846.212 Hz 
    12631.331 Hz 
    12693.272 Hz 
    14411.321 Hz 
    20178.941 Hz 
  • Example 6 AM Frequencies Employed for Treatment of Thyroid Cancer (110 Frequencies so Far Included)
  •  493.442 Hz
     517.202 Hz
     618.927 Hz
     621.321 Hz
     648.252 Hz
     663.407 Hz
     821.202 Hz
     874.341 Hz
     914.429 Hz
     941.311 Hz
     983.429 Hz
    1587.811 Hz
    1723.389 Hz
    2179.231 Hz
    2315.888 Hz
    2341.312 Hz
    2445.123 Hz
    2454.232 Hz
    2723.302 Hz
    2740.384 Hz
    2749.323 Hz
    2856.253 Hz
    2859.495 Hz
    2886.232 Hz
    3021.122 Hz
    3078.275 Hz
    3080.592 Hz
    3198.323 Hz
    3248.321 Hz
    3271.329 Hz
    3284.192 Hz
    3335.332 Hz
    3434.911 Hz
    3440.212 Hz
    3475.216 Hz
    3509.522 Hz
    3533.328 Hz
    3637.085 Hz
    3682.489 Hz
    4154.301 Hz
    4243.393 Hz
    4261.228 Hz
    4330.289 Hz
    4340.833 Hz
    4358.333 Hz
    4366.294 Hz
    4426.387 Hz
    4458.339 Hz
    4479.113 Hz
    4744.424 Hz
    4865.421 Hz
    5323.192 Hz
    5324.123 Hz
    5548.879 Hz
    5711.283 Hz
    5754.332 Hz
    6455.131 Hz
    6620.132 Hz
    6666.839 Hz
    6714.189 Hz
    6745.333 Hz
    6766.281 Hz
    6884.432 Hz
    7036.122 Hz
    7230.838 Hz
    7323.209 Hz
    7355.378 Hz
    7432.143 Hz
    7534.221 Hz
    7623.184 Hz
    7725.339 Hz
    7920.879 Hz
    8013.953 Hz
    8019.912 Hz
    8040.231 Hz
    8078.955 Hz
    8082.173 Hz
     8147.1 Hz
    8281.259 Hz
    8309.752 Hz
    8311.371 Hz
    8435.094 Hz
    8525.789 Hz
    8744.527 Hz
    9009.329 Hz
    9070.809 Hz
    10020.521 Hz 
    10039.109 Hz 
    10127.279 Hz 
    10134.161 Hz 
    10257.324 Hz 
    10498.339 Hz 
    11537.292 Hz 
    11559.292 Hz 
    11913.222 Hz 
    11927.934 Hz 
    11955.949 Hz 
    12120.049 Hz 
    12139.222 Hz 
    13636.082 Hz 
    13654.272 Hz 
    13677.211 Hz 
    14014.941 Hz 
    14445.214 Hz 
    16023.119 Hz 
    16048.391 Hz 
    17323.196 Hz 
    17577.221 Hz 
    17881.709 Hz 
    17911.323 Hz 
  • Example 7 AM Frequencies Employed for Treatment of Bladder Cancer (28 Frequencies so Far Included)
  •  623.243 Hz
     757.084 Hz
      870.4 Hz
    2454.423 Hz
    2480.191 Hz
    2581.101 Hz
    2715.232 Hz
    3042.012 Hz
    3196.194 Hz
    3265.323 Hz
    3438.109 Hz
    3692.319 Hz
    3952.308 Hz
    5230.227 Hz
    6022.942 Hz
    6061.711 Hz
    6710.899 Hz
    6721.912 Hz
    7181.784 Hz
    7458.209 Hz
     8235.21 Hz
    8749.232 Hz
    9354.812 Hz
    12532.729 Hz 
    13467.209 Hz 
     13777.9 Hz
    14015.241 Hz 
    18524.419 Hz 
  • Example 8 AM Frequencies Employed For Treatment of Colon Cancer (100 Frequencies so Far Included)
  •   78.76 Hz
     796.562 Hz
     841.541 Hz
     842.783 Hz
     914.429 Hz
    1162.117 Hz
    1372.207 Hz
    1372.934 Hz
    1718.532 Hz
    2243.169 Hz
    2278.312 Hz
     2286.5 Hz
    2286.519 Hz
    2334.178 Hz
    2423.292 Hz
    2454.423 Hz
    2464.229 Hz
    2598.853 Hz
    2623.048 Hz
    3131.123 Hz
    3161.465 Hz
    3175.313 Hz
    3249.529 Hz
    3363.229 Hz
    3373.892 Hz
    3390.925 Hz
    3409.179 Hz
    3432.274 Hz
    3509.522 Hz
    3531.422 Hz
    3533.328 Hz
    3766.296 Hz
    4040.839 Hz
    4081.022 Hz
    4123.953 Hz
    4146.274 Hz
    4233.822 Hz
    4282.332 Hz
    4318.222 Hz
    4344.082 Hz
    4416.221 Hz
    4481.242 Hz
    4724.263 Hz
    4751.319 Hz
    4755.323 Hz
    4788.485 Hz
    5149.331 Hz
    5217.402 Hz
    5386.212 Hz
    5407.192 Hz
    5426.323 Hz
    5496.434 Hz
    5555.212 Hz
    5572.032 Hz
    5634.933 Hz
    5724.231 Hz
    5758.378 Hz
    5787.342 Hz
    5948.897 Hz
    5967.448 Hz
    5976.825 Hz
    6182.322 Hz
    6292.379 Hz
    6324.493 Hz
    6341.248 Hz
    6471.322 Hz
    6477.218 Hz
    6558.342 Hz
    6855.286 Hz
    7129.843 Hz
    7140.187 Hz
    7162.422 Hz
    7368.222 Hz
    7645.859 Hz
    7829.234 Hz
    7866.229 Hz
    7877.334 Hz
    8013.314 Hz
    8374.942 Hz
    8384.228 Hz
    8408.121 Hz
    8534.111 Hz
    8568.033 Hz
    8573.122 Hz
    9226.222 Hz
     9351.9 Hz
    9737.211 Hz
    9744.193 Hz
    9942.321 Hz
    10301.371 Hz 
    10401.515 Hz 
    10872.693 Hz 
    11220.222 Hz 
    11283.378 Hz 
    12256.432 Hz 
    13749.858 Hz 
    15231.548 Hz 
    15248.324 Hz 
    58191.928 Hz 
    60317.352 Hz 
  • Example 9 AM Frequencies Employed for Treatment of Pancreas Cancer (166 Frequencies so Far Included)
  •   331.3 Hz
     331.365 Hz
      436.3 Hz
     436.332 Hz
     447.942 Hz
     476.127 Hz
     559.292 Hz
     589.187 Hz
     624.218 Hz
       727 Hz
     734.921 Hz
     809.313 Hz
     845.309 Hz
      870.4 Hz
     963.221 Hz
     1156.79 Hz
       1157 Hz
       1179 Hz
    1360.133 Hz
    1372.207 Hz
    1372.934 Hz
    1804.126 Hz
    1816.221 Hz
    1873.477 Hz
    1967.211 Hz
    1990.482 Hz
    2278.312 Hz
    2315.921 Hz
    2320.315 Hz
    2334.178 Hz
    2381.443 Hz
       2469 Hz
    2477.919 Hz
    2542.221 Hz
    2598.853 Hz
    2647.938 Hz
    2685.081 Hz
    2716.095 Hz
    2721.331 Hz
    2732.231 Hz
    2809.849 Hz
    2823.428 Hz
    2835.332 Hz
    3134.313 Hz
    3241.461 Hz
    3255.219 Hz
    3263.432 Hz
    3286.255 Hz
    3330.935 Hz
    3373.892 Hz
    3438.109 Hz
    3449.219 Hz
    3535.219 Hz
    3549.215 Hz
    3564.419 Hz
    3619.412 Hz
    3622.312 Hz
    3638.432 Hz
    3696.424 Hz
    3943.214 Hz
    3976.929 Hz
    4014.889 Hz
    4041.219 Hz
    4044.195 Hz
    4056.384 Hz
    4085.971 Hz
    4144.592 Hz
    4153.192 Hz
    4161.889 Hz
    4243.393 Hz
    4332.498 Hz
    4341.423 Hz
    4355.327 Hz
    4417.885 Hz
    4422.322 Hz
    4451.297 Hz
    4486.384 Hz
    4558.306 Hz
       4580 Hz
    4685.082 Hz
    4839.589 Hz
    5151.402 Hz
    5209.911 Hz
    5262.282 Hz
    5271.312 Hz
     5387.73 Hz
    5494.928 Hz
    5521.221 Hz
    5573.209 Hz
    5609.382 Hz
    5929.616 Hz
    5948.897 Hz
    5966.112 Hz
    5976.825 Hz
    6064.197 Hz
    6086.256 Hz
    6157.253 Hz
    6215.298 Hz
    6333.917 Hz
    6365.242 Hz
    6558.342 Hz
    6568.278 Hz
    6823.194 Hz
    6853.391 Hz
    6855.286 Hz
    7213.204 Hz
    7228.528 Hz
    7238.232 Hz
    7277.921 Hz
    7280.422 Hz
    7320.494 Hz
    7366.412 Hz
    7534.221 Hz
    7548.713 Hz
    7567.127 Hz
    7620.851 Hz
    7663.209 Hz
    7725.203 Hz
    7852.233 Hz
    7920.879 Hz
    7985.122 Hz
    8008.323 Hz
    8013.312 Hz
    8045.484 Hz
    8242.332 Hz
    8351.622 Hz
    8408.121 Hz
    8455.894 Hz
    8551.231 Hz
    8743.321 Hz
    8789.631 Hz
    8868.809 Hz
    9012.241 Hz
    9028.994 Hz
    9131.232 Hz
    9658.296 Hz
    9663.495 Hz
    9680.737 Hz
    9824.442 Hz
    9942.321 Hz
    10279.122 Hz 
    10388.49 Hz
    10438.495 Hz 
    10518.311 Hz 
    10528.239 Hz 
    10582.095 Hz 
    10926.111 Hz 
    10948.411 Hz 
    10955.558 Hz 
    11538.193 Hz 
    11904.741 Hz 
    12255.229 Hz 
    12613.341 Hz 
    12819.942 Hz 
    13674.482 Hz 
    13731.322 Hz 
    14525.312 Hz 
    14537.218 Hz 
    14549.331 Hz 
    14845.453 Hz 
    14944.989 Hz 
    15246.315 Hz 
    18668.239 Hz 
    19321.231 Hz 
    19347.208 Hz 
    30182.932 Hz 
  • Example 10 AM Frequencies Employed for Treatment of Lung Cancer (80 Frequencies so Far Included)
  •  304.148 Hz
      694.7 Hz
     694.727 Hz
      708.8 Hz
     708.841 Hz
    1587.811 Hz
    1759.318 Hz
    1873.477 Hz
    2253.704 Hz
    2391.312 Hz
    2454.232 Hz
    2729.929 Hz
    2741.261 Hz
    2761.312 Hz
    2784.491 Hz
    2812.443 Hz
    2855.218 Hz
    2859.495 Hz
    3128.822 Hz
    3139.297 Hz
    3193.212 Hz
    3348.783 Hz
    3360.971 Hz
    3366.311 Hz
    3373.892 Hz
    3440.212 Hz
    3461.322 Hz
    3682.489 Hz
    3727.231 Hz
    3749.882 Hz
    3769.942 Hz
    4131.235 Hz
    4158.393 Hz
    4243.393 Hz
    4347.733 Hz
    4373.411 Hz
    4378.321 Hz
    4416.221 Hz
    4481.242 Hz
    4777.521 Hz
    4798.422 Hz
    4837.241 Hz
    4959.842 Hz
    5013.321 Hz
    5047.523 Hz
    5068.322 Hz
    5371.922 Hz
    5538.432 Hz
    5548.879 Hz
    5679.309 Hz
    5734.143 Hz
    5787.342 Hz
    6445.309 Hz
    6838.434 Hz
    6870.955 Hz
    6879.216 Hz
    7079.411 Hz
    7216.288 Hz
    7376.089 Hz
    7761.289 Hz
    8082.173 Hz
    8281.259 Hz
    8352.189 Hz
    8442.473 Hz
    8773.916 Hz
    8935.752 Hz
    9121.223 Hz
    9181.434 Hz
    9317.913 Hz
    9363.896 Hz
    9736.919 Hz
    9753.321 Hz
    10424.908 Hz 
    10452.913 Hz 
    10824.609 Hz 
    11656.329 Hz 
    12748.919 Hz 
    15774.291 Hz 
    15798.333 Hz 
    16510.321 Hz 
  • Example 11 AM Frequencies Employed for Treatment of Leiomyosarcoma (36 Frequencies so Far Included)
  •  836.923 Hz
     843.181 Hz
    1411.241 Hz
    2073.721 Hz
    2381.443 Hz
    2711.019 Hz
    2911.329 Hz
    3232.185 Hz
    3518.321 Hz
    3544.209 Hz
    3569.219 Hz
    4233.822 Hz
    4241.321 Hz
    4266.591 Hz
    4337.322 Hz
    4424.112 Hz
    4436.111 Hz
     4485.22 Hz
    5545.521 Hz
    5577.841 Hz
    5631.422 Hz
    5696.184 Hz
    6472.098 Hz
    6558.342 Hz
    6651.276 Hz
    7168.892 Hz
    7406.309 Hz
    7452.528 Hz
    7649.209 Hz
    7808.352 Hz
    9040.313 Hz
    9074.294 Hz
    9189.092 Hz
    9484.512 Hz
    9943.972 Hz
    12086.394 Hz 
  • Example 12 AM Frequencies Employed for Treatment of Mesothelioma (16 Frequencies so Far Included)
  •  958.929 Hz
    1713.913 Hz
    1736.782 Hz
    2334.178 Hz
    2607.193 Hz
    3112.974 Hz
    3319.945 Hz
    3449.219 Hz
    3622.312 Hz
    5151.402 Hz
    5887.022 Hz
    5965.922 Hz
    6516.793 Hz
    7224.197 Hz
    9471.152 Hz
    14617.393 Hz 
  • Example 13 AM Frequencies Employed for Treatment of Neuro-Endocrine (30 Frequencies so Far Included)
  • 1766.335 Hz
    2408.225 Hz
    2441.502 Hz
    2647.938 Hz
    2741.261 Hz
    3020.212 Hz
    3128.822 Hz
    3238.742 Hz
    3296.431 Hz
    3348.783 Hz
    3360.971 Hz
    3440.212 Hz
    3533.328 Hz
    3666.283 Hz
    4079.282 Hz
    4243.393 Hz
    4426.387 Hz
    5245.818 Hz
    5536.242 Hz
    5548.879 Hz
    5739.422 Hz
    5849.241 Hz
    6291.631 Hz
    6406.891 Hz
    6780.679 Hz
    7151.264 Hz
    7482.245 Hz
    7575.393 Hz
    8359.932 Hz
    9073.418 Hz
  • Example 14 AM Frequencies Employed for Treatment of Leukemia and Chronic Lymphoid Cancer (17 Frequencies so Far Included)
  •  814.413 Hz
     825.145 Hz
    2415.243 Hz
    2436.316 Hz
    2874.432 Hz
    2891.029 Hz
    3361.671 Hz
    5245.452 Hz
    5557.333 Hz
    6850.197 Hz
    6919.322 Hz
    7587.224 Hz
    7629.318 Hz
    8172.405 Hz
    8272.338 Hz
    8438.453 Hz
    12950.331 Hz 
  • Example 15 AM Frequencies Employed for Treatment of Myeloma, Multiple Cancer (20 Frequencies so Far Included)
  •  765.196 Hz
    2336.238 Hz
    2372.122 Hz
    2381.443 Hz
    2425.394 Hz
    2656.339 Hz
    2741.261 Hz
    2883.618 Hz
    2919.273 Hz
    3265.323 Hz
    3564.455 Hz
     3580.25 Hz
    3584.291 Hz
    3674.292 Hz
    5249.331 Hz
    7967.311 Hz
    7973.125 Hz
    8049.952 Hz
    8283.329 Hz
    10351.323 Hz 
  • Example 16 AM Frequencies Employed for Treatment of Hodgkin Disease (Lymphoma) (19 Frequencies so Far Included)
  •   752.5 Hz
      976.3 Hz
    1558.223 Hz
    2310.912 Hz
    2477.919 Hz
    2560.843 Hz
    3348.783 Hz
    3371.216 Hz
    3605.432 Hz
    3623.198 Hz
    3838.281 Hz
     3838.48 Hz
       5102 Hz
    5696.932 Hz
    5724.231 Hz
    6358.194 Hz
    7472.211 Hz
    8062.121 Hz
    8222.222 Hz
  • Example 17 AM Frequencies Employed for Treatment of Brain Cancer (57 Frequencies so Far Included)
  • 1372.934 Hz
    2318.182 Hz
    2381.443 Hz
    2425.394 Hz
    2442.423 Hz
    2478.973 Hz
    2654.513 Hz
    2661.324 Hz
    2686.105 Hz
    2690.179 Hz
    3249.332 Hz
    3277.509 Hz
    3335.279 Hz
    3348.783 Hz
    3436.211 Hz
    3916.321 Hz
    4031.933 Hz
    4086.091 Hz
    4241.321 Hz
    4318.222 Hz
     4334.33 Hz
    4358.333 Hz
    4393.419 Hz
    4454.194 Hz
    4515.789 Hz
    4619.324 Hz
    4723.937 Hz
    4853.286 Hz
    5289.231 Hz
    5378.099 Hz
    5426.323 Hz
    5640.981 Hz
    6316.211 Hz
    6459.203 Hz
    6474.332 Hz
    6626.572 Hz
    6855.286 Hz
    6915.886 Hz
    6943.386 Hz
    7151.264 Hz
    7182.922 Hz
    7194.897 Hz
    7323.209 Hz
    7390.343 Hz
    7796.221 Hz
    7961.122 Hz
    8128.942 Hz
    8245.109 Hz
    8272.281 Hz
    8358.154 Hz
    8408.121 Hz
     9138.82 Hz
    10719.318 Hz 
    11556.241 Hz 
    12828.633 Hz 
    14515.962 Hz 
    14586.765 Hz 
  • The above Examples reflect AM frequencies determined by a bio-feedback procedure involving very substantial observations and measurements of physiological responses (at certain well defined AM frequencies) by subjects exposed to low energy electromagnetic emission excitation. In general, it is recommended that all of the listed frequencies be applied in the treatment of subjects suffering from the indicated form of cancer. However, a limited number of the listed frequencies also lead to beneficial effects.
  • Of note in respect of the above listed frequencies, in particular those Examples including a large number of frequencies, it has earlier on been determined that beneficial therapeutic effects are achieved by application of some but not all of the frequencies listed. However, following on more extended trials, it has been determined that application to subjects of further frequencies enhance the efficacy of treatment and yields therapeutic effects in patients whose tumours have become resistant to therapy. It is accordingly preferred that all of the determined listed frequencies be applied to the subject. The mechanism of including additional frequencies is attributed to either or both of inter-active synergism between applied frequencies or between cells which have been influenced by the treatment and additive effects of the additional frequencies.
  • Of further note is the fact that different patients suffering from the same type of tumour cell growth practically invariably exhibit the above-mentioned physiological responses at the same well defined AM frequencies. Furthermore, AM frequencies which differ only very slightly (less than 0.0001% at higher frequencies) from the frequencies listed, in general elicit no physiological response by subjects exposed to excitation at such very slightly different frequency. In view of these determinations, the electronic system of the present invention may be adapted to screen a subject for physiological responses over a broad range of frequencies to determine the presence or absence tumour cells and, if positive, then to note at which defined frequencies physiological responses are elicited. These frequencies will in general match with the defined frequencies listed in one or other of the Examples above or such further examples as may be developed and hence the nature of the tumour will be known. The electronic system of the invention is therefore a valuable diagnostic tool for diagnosing the presence or absence and identities of types of tumour cell growths or cancers. Furthermore, the electronic system of the invention is of value for predicting whether a patient will benefit from the application of a given series of modulation frequencies. The system therefore possesses a capability of predicting responses to treatment, thereby enhancing the possibility to select optimal modes of treatment.
  • The sequence of well defined frequencies are preferably applied sequentially for determined periods of time, e.g. 3 seconds for each frequency, but several frequencies may also be applied simultaneously. This means that a cycle of application involving 180 frequencies would take nearly 10 minutes time. Advantageous effects may however also arise from applying individual well defined frequencies for differing time periods, e.g. some for 3 seconds, some for 6 seconds, etc. . . . .
  • Therapeutic dosages to be applied to a subject suffering from the presence of tumour cell growth or cancer are determined by the time of application of the low energy electromagnetic emissions to the subject and will depend on the nature of the cancer and the overall condition of the subject. In general, however, greatest experience has been gained in treating terminally ill subjects expected to survive no longer than about three months and who have agreed to discontinue alternative forms of cancer treatments such as chemo-therapy or radioactive treatment. In these severe cases, lengthy times of treatment are recommended, e.g. 3 times 1 hour daily treatment. However, with the development of alternative forms of application, i.e. other than by means of a mouth probe, continuous application is possible and is likely to enhance compliance and the efficacy of the treatment.
  • While the invention has been described with specific embodiments, other alternatives, modifications, and variations will be apparent to those skilled in the art. Accordingly, it will be intended to include all such alternatives, modifications, and variations within the spirit and scope of the appended claims.

Claims (19)

1-18. (canceled)
19. An electronic system activatable by electrical power and structured to influence cellular functions or malfunctions in a warm-blooded mammalian subject, said electronic system comprising at least one controllable low energy electromagnetic energy generator circuit for generating one or more high frequency carrier signals, at least one data processor constructed and arranged for communication with the at least one generator circuit and for receiving control information from a source of control information, said at least one generator circuit including at least one amplitude modulation control signal generator for controlling amplitude modulated variations of the one or more high frequency carrier signals, said at least one generator circuit furthermore including at least one programmable amplitude modulation frequency control signal generator for controlling a frequency at which amplitude modulations are generated, the system furthermore comprising a connection position for connection to an electrically conductive applicator for applying to the warm-blooded mammalian subject one or more amplitude-modulated low energy emissions at a program-controlled frequency, wherein said at least one programmable amplitude frequency control generator is adapted to accurately control the frequency at which said amplitude modulations are generated to within an accuracy of at least 1000 ppm relative to one or more determined or predetermined reference amplitude modulation frequencies selected from within a range of 0.01 Hz to 70 kHz and wherein said source of control information includes reference amplitude modulation frequency control information which comprises at least a significant proportion (in excess of 50%) of accurately defined reference amplitude modulation frequencies listed in any one of Examples A, B and 1 to 17, or all of said accurately defined frequencies or yet further accurately defined frequencies, or combinations thereof.
20. The system according to claim 19, wherein the frequency of one or more of the amplitude modulations generated are controllable to within an accuracy of 100 ppm relative to the one or more determined or predetermined reference amplitude modulation frequencies.
21. The system according to claim 20, wherein the frequency of one or more of the amplitude modulations generated are controllable to within an accuracy of 10 ppm relative to the one or more determined or predetermined reference amplitude modulation frequencies.
22. The system according to claim 21, wherein the frequency of one or more of the amplitude modulations generated are controllable to within an accuracy of about 1 ppm relative to the one or more determined or predetermined reference amplitude modulation frequencies.
23. The system according to claim 19, wherein the one or more amplitude modulated low energy emissions generated are maintained at a stability during emission of at least 10−5.
24. The system according to claim 23, wherein a stability of at least 10−6 is maintained.
25. The system according to claim 24, wherein a stability of at least 10−7 is maintained.
26. The system according to claim 19, wherein said at least one controllable generator circuit is controllable by amplitude modulation control signals which lead to various forms of amplitude modulation wave forms being generated.
27. The system according to claim 26, wherein the amplitude modulation wave forms are selected from sinusoidal, square, triangular or multiple combinations thereof.
28. The system according to claim 26, wherein the at least one generator circuit is controllable by amplitude modulation control signals which generate a plurality of amplitude modulation wave forms, either sequentially or simultaneously.
29. The system according to claim 19, wherein the one or more high frequency carrier signals generated by the at least one generator circuit are selected from one or more high frequencies selected from about 27 MHz, 433 MHz and 900 MHz.
30. The system according to claim 19, wherein the system further comprises one or more interfaces communicating with the at least one data processor, and wherein the control information is transferable to said one or more interfaces and hence to the at least one data processor to enable command signals responsive to received control information to be communicated to the at least one generator circuit by the at least one data processor.
31. The system according to claim 30, wherein the control information is transferable over a communication link to the at least one data processor via the one or more interfaces communicating with the at least one data processor.
32. The system according to claim 30, wherein the control information is stored in an information storage device and wherein the control information is transferable to the at least one data processor via said one or more interfaces communicating with the at least one data processor.
33. The system according to claim 30, wherein the system further comprises a user identification device communicating with at least one of the at least one data processor to enable the system to be activated for use only by the user.
34. The system according to claim 19, further comprising a monitor comprising monitoring software for monitoring the amplitude and the amplitude modulation frequency of the amplitude modulated low energy electromagnetic emissions generated by the at least one generator circuit.
35. The system according to claim 19, wherein the determined or predetermined amplitude modulation frequency control information is determined or predetermined by a bio-feedback process involving observations or measurements of physiological reactions by the subject during a time that cellular functions of the subject are excited by exposing the subject to emissions of high frequency carrier signals amplitude modulated at a series of amplitude modulation frequencies.
36. The system according to claim 35, wherein the determined or predetermined frequencies are employed as a mode to identify a nature of a tumor or cancer harbored by the warm-blooded mammalian subject.
US12/450,450 2007-03-27 2008-03-26 Electronic system for influencing cellular functions in a warm-blooded mammalian subject Abandoned US20100042168A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP07006320.1 2007-03-27
EP07006320A EP1974769A1 (en) 2007-03-27 2007-03-27 Electronic system for influencing cellular functions in a warm-blooded mammalian subject
PCT/EP2008/002379 WO2008116640A2 (en) 2007-03-27 2008-03-26 Electronic system for influencing cellular functions in a warm-blooded mammalian subject

Publications (1)

Publication Number Publication Date
US20100042168A1 true US20100042168A1 (en) 2010-02-18

Family

ID=38117246

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/450,450 Abandoned US20100042168A1 (en) 2007-03-27 2008-03-26 Electronic system for influencing cellular functions in a warm-blooded mammalian subject
US13/573,104 Active 2030-03-12 US8977365B2 (en) 2007-03-27 2012-08-22 Electronic system for influencing cellular functions in a warm-blooded mammalian subject

Family Applications After (1)

Application Number Title Priority Date Filing Date
US13/573,104 Active 2030-03-12 US8977365B2 (en) 2007-03-27 2012-08-22 Electronic system for influencing cellular functions in a warm-blooded mammalian subject

Country Status (20)

Country Link
US (2) US20100042168A1 (en)
EP (2) EP1974769A1 (en)
JP (1) JP5435240B2 (en)
KR (1) KR101474582B1 (en)
CN (1) CN101663065B (en)
AU (1) AU2008232041C1 (en)
BR (1) BRPI0810084B1 (en)
CA (1) CA2682322C (en)
DK (1) DK2139557T3 (en)
ES (1) ES2545103T3 (en)
HU (1) HUE027033T2 (en)
IL (1) IL201099A (en)
MX (1) MX2009010425A (en)
PL (1) PL2139557T3 (en)
PT (1) PT2139557E (en)
RU (1) RU2594824C2 (en)
SA (1) SA08290168B1 (en)
SI (1) SI2139557T1 (en)
WO (1) WO2008116640A2 (en)
ZA (1) ZA200906700B (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120310033A1 (en) * 2009-12-23 2012-12-06 Axel Muntermann Method for Cosmetic Skin Smoothening and Device Therefor
WO2014164924A1 (en) * 2013-03-11 2014-10-09 NeuroEM Therapeutics, Inc. Electromagnetic treatment of brian and body disorders
ES2535696A1 (en) * 2013-11-13 2015-05-13 Joaquín SUROS FRIGOLA Generator of am and fm waves for the practice of electrotherapy (Machine-translation by Google Translate, not legally binding)
WO2019075391A1 (en) 2017-10-13 2019-04-18 Costa Frederico Perego System for characterization, diagnosis, and treatment of a health condition of a patient and microtubule conductivity, and methods of using same
US20190217111A1 (en) * 2013-03-11 2019-07-18 NeuroEM Therapeutics, Inc. Systems for sensing proper emitter array placement
CN110248696A (en) * 2017-07-21 2019-09-17 耀姿玛碧艾姆科技有限公司 Oral cavity high frequency treatment instrument
US11752356B2 (en) 2013-03-11 2023-09-12 NeuroEM Therapeutics, Inc. Systems for controlling power to differently loaded antenna arrays
US11759650B2 (en) 2013-03-11 2023-09-19 NeuroEM Therapeutics, Inc. Immunoregulation, brain detoxification, and cognitive protection by electromagnetic treatment
US11794028B2 (en) 2014-03-11 2023-10-24 NeuroEM Therapeutics, Inc. Transcranial electromagnetic treatment
US11911629B2 (en) 2013-03-11 2024-02-27 NeurEM Therapeutics, Inc. Treatment of primary and metastatic brain cancers by transcranial electromagnetic treatment

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8926990B2 (en) 2009-10-13 2015-01-06 Rutgers, The State University Of New Jersey Treatment and diagnosis of inflammatory disorders and HIV
ITPD20090279A1 (en) * 2009-09-25 2011-03-26 Hypothesis Srl DEVICE FOR PREVENTING DEEP VENOUS THROMBOSIS
WO2012143667A2 (en) * 2011-04-18 2012-10-26 Freewave Ltd Therapeutic apparatus
WO2012030248A1 (en) * 2010-09-03 2012-03-08 Sajphutdinov Marat Kadirovich Electromagnetic contact-free therapy system
ITBO20110125A1 (en) * 2011-03-16 2012-09-17 Project Di Gaudenzi Valter DEVICE FOR BODY APPLICATIONS
ITNA20110019A1 (en) * 2011-04-28 2012-10-29 Attilio Grattacaso EQUIPMENT, SYSTEM AND METHOD FOR CONTRACTION AND JOINT DIATHERMY BY MODULATION AND RADIOFREQUENCY
CN102353848B (en) * 2011-07-01 2013-08-28 大连海事大学 Electromagnetic radiation experimental system for cell
RU2514344C1 (en) * 2012-12-05 2014-04-27 Государственное бюджетное образовательное учреждение высшего профессионального образования "Самарский государственный медицинский университет" Министерства здравоохранения Российской Федерации (ГБОУ ВПО СамГМУ Минздрава России) Vestibuloplasty technique
US9784263B2 (en) 2014-11-06 2017-10-10 Zoll Circulation, Inc. Heat exchange system for patient temperature control with easy loading high performance peristaltic pump
US11359620B2 (en) 2015-04-01 2022-06-14 Zoll Circulation, Inc. Heat exchange system for patient temperature control with easy loading high performance peristaltic pump
US20160317050A1 (en) 2015-04-28 2016-11-03 Federico Perego Costa Hemodynamic parameter (Hdp) monitoring system for diagnosis of a health condition of a patient
US11185440B2 (en) 2017-02-02 2021-11-30 Zoll Circulation, Inc. Devices, systems and methods for endovascular temperature control
US11071876B2 (en) * 2018-12-03 2021-07-27 Aah Holdings Llc Apparatus and method for treatment of mental and behavioral conditions and disorders with electromagnetic fields
EP3952735A4 (en) * 2019-04-10 2023-01-11 Autem Medical, LLC System for prognosticating patient outcomes and methods of using the same
CN114786608A (en) * 2019-10-21 2022-07-22 仿生治疗股份有限公司 Electrical system for treating a subject
EP4072656A2 (en) 2019-12-11 2022-10-19 Novocure GmbH Compositions and methods for imaging a cell
US20210178155A1 (en) 2019-12-11 2021-06-17 Novocure Gmbh Compositions And Methods Of Altering The Electric Impedance To An Alternating Electric Field
IL293417A (en) 2019-12-11 2022-07-01 Novocure Gmbh Methods of altering the electric impedance to an alternating electric field
JP2023525083A (en) 2020-05-08 2023-06-14 ノボキュア ゲーエムベーハー Compositions and methods for applying an alternating electric field to pluripotent stem cells

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4649935A (en) * 1984-05-21 1987-03-17 Symtonic Sa Method of treating neurovegetative disorders and apparatus therefor
US5441528A (en) * 1992-09-25 1995-08-15 Symtonic, S.A. Method and system for applying low energy emission therapy
US5690692A (en) * 1995-10-11 1997-11-25 Regeneration Technology Bio-active frequency generator and method
US5908441A (en) * 1997-01-16 1999-06-01 Bare; James E. Resonant frequency therapy device
US6167304A (en) * 1993-05-28 2000-12-26 Loos; Hendricus G. Pulse variability in electric field manipulation of nervous systems
US20050090732A1 (en) * 2003-10-28 2005-04-28 Triton Biosystems, Inc. Therapy via targeted delivery of nanoscale particles

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07171222A (en) * 1993-12-21 1995-07-11 Olympus Optical Co Ltd Thermotherapeutic apparatus
RU2112563C1 (en) * 1995-03-14 1998-06-10 Синицын Лев Николаевич Method for treating purulent wounds
US5891182A (en) 1995-10-11 1999-04-06 Regeneration Tech Bio-active frequency generator and method
US6246912B1 (en) * 1996-06-27 2001-06-12 Sherwood Services Ag Modulated high frequency tissue modification
RU2127616C1 (en) * 1998-02-03 1999-03-20 Закрытое акционерное общество НЦИМ "ЛИДО" Device for millimeter-wave therapy
EP0966988A1 (en) 1998-06-24 1999-12-29 Santi Tofani Apparatus and method for interfering with pathological cells survival
US6530630B2 (en) * 2001-07-13 2003-03-11 Carrier Corporation Panel seal for an air handling unit
JP4664661B2 (en) * 2004-12-15 2011-04-06 株式会社東芝 Radiation therapy management system

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4649935A (en) * 1984-05-21 1987-03-17 Symtonic Sa Method of treating neurovegetative disorders and apparatus therefor
US4765322A (en) * 1984-05-21 1988-08-23 Symtonic Sa Method of treating neurovegetative disorders and apparatus therefor
US5441528A (en) * 1992-09-25 1995-08-15 Symtonic, S.A. Method and system for applying low energy emission therapy
US6167304A (en) * 1993-05-28 2000-12-26 Loos; Hendricus G. Pulse variability in electric field manipulation of nervous systems
US5690692A (en) * 1995-10-11 1997-11-25 Regeneration Technology Bio-active frequency generator and method
US5908441A (en) * 1997-01-16 1999-06-01 Bare; James E. Resonant frequency therapy device
US20050090732A1 (en) * 2003-10-28 2005-04-28 Triton Biosystems, Inc. Therapy via targeted delivery of nanoscale particles

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9643026B2 (en) * 2009-12-23 2017-05-09 Axel Muntermann Method for cosmetic skin smoothening and device therefor
US20120310033A1 (en) * 2009-12-23 2012-12-06 Axel Muntermann Method for Cosmetic Skin Smoothening and Device Therefor
US11759650B2 (en) 2013-03-11 2023-09-19 NeuroEM Therapeutics, Inc. Immunoregulation, brain detoxification, and cognitive protection by electromagnetic treatment
US20190217111A1 (en) * 2013-03-11 2019-07-18 NeuroEM Therapeutics, Inc. Systems for sensing proper emitter array placement
US10765879B2 (en) 2013-03-11 2020-09-08 NeuroEM Therapeutics, Inc. Electromagnetic treatment of brain and body disorders
US11752356B2 (en) 2013-03-11 2023-09-12 NeuroEM Therapeutics, Inc. Systems for controlling power to differently loaded antenna arrays
WO2014164924A1 (en) * 2013-03-11 2014-10-09 NeuroEM Therapeutics, Inc. Electromagnetic treatment of brian and body disorders
US11813472B2 (en) * 2013-03-11 2023-11-14 NeuroEM Therapeutics, Inc. Systems for sensing proper emitter array placement
US11911629B2 (en) 2013-03-11 2024-02-27 NeurEM Therapeutics, Inc. Treatment of primary and metastatic brain cancers by transcranial electromagnetic treatment
ES2535696A1 (en) * 2013-11-13 2015-05-13 Joaquín SUROS FRIGOLA Generator of am and fm waves for the practice of electrotherapy (Machine-translation by Google Translate, not legally binding)
US11794028B2 (en) 2014-03-11 2023-10-24 NeuroEM Therapeutics, Inc. Transcranial electromagnetic treatment
CN110248696A (en) * 2017-07-21 2019-09-17 耀姿玛碧艾姆科技有限公司 Oral cavity high frequency treatment instrument
WO2019075391A1 (en) 2017-10-13 2019-04-18 Costa Frederico Perego System for characterization, diagnosis, and treatment of a health condition of a patient and microtubule conductivity, and methods of using same

Also Published As

Publication number Publication date
RU2009139633A (en) 2011-05-10
WO2008116640A3 (en) 2008-11-27
US20130079853A1 (en) 2013-03-28
BRPI0810084A2 (en) 2014-03-18
CA2682322C (en) 2015-07-14
CN101663065B (en) 2014-04-16
WO2008116640A2 (en) 2008-10-02
CN101663065A (en) 2010-03-03
RU2594824C2 (en) 2016-08-20
KR101474582B1 (en) 2014-12-19
US8977365B2 (en) 2015-03-10
EP2139557A2 (en) 2010-01-06
PL2139557T3 (en) 2015-10-30
IL201099A (en) 2014-05-28
EP2139557B1 (en) 2015-05-13
MX2009010425A (en) 2009-12-14
KR20100015970A (en) 2010-02-12
ZA200906700B (en) 2010-11-24
BRPI0810084B1 (en) 2016-04-12
HUE027033T2 (en) 2016-08-29
SI2139557T1 (en) 2015-10-30
IL201099A0 (en) 2010-05-17
DK2139557T3 (en) 2015-08-10
AU2008232041A2 (en) 2010-03-25
AU2008232041C1 (en) 2014-02-20
JP2010522051A (en) 2010-07-01
JP5435240B2 (en) 2014-03-05
AU2008232041A1 (en) 2008-10-02
ES2545103T3 (en) 2015-09-08
AU2008232041B2 (en) 2013-11-14
EP1974769A1 (en) 2008-10-01
PT2139557E (en) 2015-09-23
CA2682322A1 (en) 2008-10-02
SA08290168B1 (en) 2013-04-30

Similar Documents

Publication Publication Date Title
US8977365B2 (en) Electronic system for influencing cellular functions in a warm-blooded mammalian subject
JP5840774B2 (en) Far field radiant power supply for implantable medical treatment delivery devices
CN108064147B (en) Hemodynamic parameter (HDP) monitoring system for diagnosing a health condition of a patient
Habibagahi et al. Vagus nerve stimulation using a miniaturized wirelessly powered stimulator in pigs
US20220379130A1 (en) Electrical system for treatment of a subject
OA20699A (en) Electrical system for treatment of a subject
RU2139114C1 (en) Device for treatment of tumors, viral and bacterial diseases
RU2799358C2 (en) Methods and devices for aesthetic therapy of biological structures using radio frequency and magnetic energy
RU2134597C1 (en) Apparatus for microwave therapy
JP2001517975A (en) Therapeutic device and method
Levendag et al. Interstitial radiation and/or interstitial hyperthermia for advanced and/or recurrent cancers in the head and neck: a pilot study
Urbina et al. Electromagnetic Susceptibility of Implan table Medical Devices: An Experimental Assessment
CN109806502A (en) A kind of heart medical physiotherapy device
RU2295988C2 (en) Method and device for carrying out electromagnetotherapy
CN101332337A (en) Physiotherapy therapeutic equipment and operation method thereof

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: EXPRESSLY ABANDONED -- DURING EXAMINATION

AS Assignment

Owner name: THERABIONIC, LLC, ALABAMA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:PASCHE, BORIS, MR.;BARBAULT, ALEXANDRE, MR.;SIGNING DATES FROM 20140209 TO 20140210;REEL/FRAME:032179/0915