Cytotron Therapy :: Treating Cancer Differently

FAQs on CYTOTRON

  • CYTOTRON® is a novel, proven, state-of-the-art, innovative Class IIa therapeutic device used for the treatment of Neoplastic disorders (Cancer). The device delivers precisely computed doses of RF waves in the presence of instantaneous Rotational Magnetic field called Fast Radio Bursts (FRB)
  • CYTOTRON® uses a novel treatment modality registered as RFQMRT or Rotational Field Quantum Magnetic Resonance (RFQMR) Technology. RFQMR utilizes non-thermal, non-ionizing radio frequency waves and hence does not have any known adverse side effects.
  • RFQMR Technology produces high powered, rotational field, multi-frequency, high energy, spinning Quantum electromagnetic resonating beam in the lower end of the electromagnetic (EM) spectrum.
  • CYTOTRON® is a breakthrough, patented, novel medical device which has received relevant safety clearances.
  • CYTOTRON® was granted “Breakthrough Device Designation’ by US FDA for treatment of Breast, Liver and Pancreatic Cancers.
  • CYTOTRON® is licenced in India by Central Drugs Standard Control Organisation (CDSCO) as a therapeutic device for treating protein linked abnormally regenerating disorders (Cancer) enabling tissue apoptosis and preventing metastasis.
  • CYTOTRON therapy is a non-invasive and painless treatment modality with no known adverse side effects.

CYTOTRON® has evolved using Magnetic Resonance Imaging (MRI) based on intrinsic proton density (PD) measurements of target tissue to manipulate biophysical cellular signalling. Highly complex Fast Radio Busts (FRB) in the safe radio frequency, in the presence of controlled, high, instantaneous Magnetic Resonance, is precisely focused on target tissues to alter the Transmembrane potential (TMP) of cells which triggers apoptosis (programmed cell death) and stops growth of solid tumours.

Cells in our body can multiply up to approx 50 times before becoming senescent, which means it can no longer further that process. After the 50th division, there is a flag planted down, where a protein called p53, a programmed cell death protein, is expressed. This ensures the cell doesn’t divide any further. This process is driven by the pro-apoptotic protein p53, which regulates apoptosis. Unfortunately, in cancer cells, this process doesn’t happen because the protein is mutated or is not expressed, as they do not receive the signal to do so. Naturally, these cells don’t know when to stop multiplying and eventually progress to grow as an organ in the body or a life form. As they grow, they land up with a resource crunch. Then, these cells look at forming new colonies and start spreading with their “survival instincts” taking over. Cancer produces a very special kind of cell, called EMT cells or cancer stem cells (CSCs), that spread to another location and then it builds up new colonies.

As long as the cancer is growing, the body’s immune system does not attack it. On the contrary, it protects the cancer tissue. Cancer cells take advantage of this situation, and conquer different organs of the body, until the body cannot function normally.

CYTOTRON® is used to non-invasively re-activate the body’s tumor suppression mechanism by targeting high precision, calibrated doses of fast radio bursts (FRB) - non-ionising, non-thermal electromagnetic waves at the tumor site.  This triggers the production of new tumor suppressing nucleoproteins which determines and flags that the cell is old enough to die. The moment this happens, the cell stops growing and the immune system flushes the cell out over a period of time. The cancer tissue may be recycled, and this therapy process also works to convert or transform the cancer stem cells into cells that don’t multiply. Depending on which stage of cancer you’re being treated at, it stops the cancer cells from spreading. The earlier you get the Cytotron therapy, the cancer gets arrested at that point. Once we stop the tumor from growing and spreading, there are other ways we can manage the disease.

CYTOTRON® acts on the mitochondrial membrane and interfere with communication between the gene transcription machinery and the protoplasmic glycoproteinic complexes involved in the promotion of cellular mitosis. Based on the outcomes reported in treating malignant lesions, the CYTOTRON®  induces such alterations of the TMP in a controlled manner, to modify cellular command and control and alter cellular activity to stabilize and arrest tumor progression.

No, Non-solid tumour like Leukemia and Multiple Myeloma is not possible to be treated with CYTOTRON®.

  • The patient history and reports are scrutinized by the Medical Director /team of Doctors at the center. The reports that are required are latest PET-CT, Blood reports; CBC, LFT, RFT, Electrolytes, Serum Zinc, Copper, Magnesium, Iron, Vitamin D, Vitamin B12, HIV 1 & 2 Elisa, HCV Elisa, HBsAG Elisa, Anti Varicella, etc as required.
  • Patient presence is a must during evaluation.
  • A whole body MRI for tissue proton density determination is done to compute individualized dosimetry to target solitary (Single lesion /Brain) or multiple regions of interest (multiple lesion / widespread metastasis) in the whole body simultaneously.
  • A 2D Proton Density (PD) sequence of the tumor is obtained on film and copied by the radiologist for use at the treatment center for dose planning
  • A very low intensity Computerized Tomography (CT) guided surface marking of the Region of Interest (target tissue) is made by the radiologist.
  • The CD containing PD images is loaded into the Cytotron Central Control Unit (CCU) and the region(s) of interest is/are identified. The largest and smallest diameter of each lesion is marked. A margin of 1-2 mm beyond the target area is marked to include any infiltrating, rapidly growing tumor cells around the lesion and included in the region of interest.
  • The sequence of dose planning is set in motion automatically by the Central Control Unit, applying pre-planned proprietary algorithms
  • The patient is dosed for one hour every day for a period of 28 consecutive days without a break. If there is break for more than 24 – 48 hours before the completion of the treatment period, the treatment has to start all over again.
  • Cytotron device is operated ONLY by fully trained and Certified Cytotron technologist (Nursing & Para Nursing staff) and specialist (Medical doctors)

The therapy is for 28 hours spread over 28 days (One Hour/day). So far, over 800 patients have been treated with Cytotron, most of them in terminal stages.

One of the most striking differences that patients notice within 10-12 days of therapy is pain relief, without the need for medication. They are able to sleep better. They will also notice a marked sense of wellbeing and improved appetite. Overall survival and tumor stability and tumor progression is measured and followed up for 12 months. Over 71% terminally ill patients had stable disease one month after completion of Cytotron therapy. We maintain meticulous records of our patient’s progress and follow up, by way of both quality and quantity of life.

Patient will be reviewed periodically based on the blood reports, PET CT / MRI to compare and study the efficacy of the treatment in terms of measureable changes in dimensions, tumour volume and signal intensity differences between pre and post-treatment of targeted lesions. Regular review is a critical requirement of the treatment protocol as advised by the Medical Director of the center.

The Stay and food for the patient and one attendant is organised for the selected patients who will undergo the Dheergayu program along with Cytotron.

Cytotron therapy is a treatment modality that helps in stabilizing the tumor and arresting tumor progression in about 80% of patients in a very unique way, without collateral damage. This emerging treatment modality can be a very useful in improving the Quality of Life (QoL) and it is expected that it may soon become integral to mainstream cancer medicine.

  • Safe, Non-invasive, No Pain
  • No toxic drugs, no side effects, fatigue or depression.
  • Outpatient treatment, No Hospitalization.
  • No anesthesia, cut, scar, blood transfusion
  • No treatment complication or infection
  • Possible in surgery unfit patients
  • Cost effective.

Yes, below mentioned patients cannot take Cytotron Treatment:

  • Those patients with electrically, magnetically or mechanically activated implants (cardiac pacemakers, bio-stimulators, neuro-stimulators, cochlear implants, hearing aids)
  • Pregnancy
  • MRI incompatible implants
  • Stents near target area
  • Critically ill patients (like needing life support)
  • Mentally challenged patients
  • Patients who have inability to lie in a supine position with minimal movement for the duration of the therapy (1 hour)
  • Any other medical contra-indicatives found during screening and evaluation by the Medical Director / Medical team at the center

Device risk from the point of view of performance, electromagnetic hazard, patient and operator safety in accordance with the recommendations of International Commission for Non-Ionizing Radiation Protection (ICNIRP) was evaluated and observed by the agency that both electric and magnetic field emissions from the CYTOTRON are well below the hazardous levels specified by ICNIRP for the measured frequency band and safe to be used on human biological systems. 

The Cytotron is programmed to affect only target tissues (proton dense tumours) non-invasively, sparing surrounding normal tissues.  This is in contradistinction with conventional ionizing radiotherapy, which explains the absence of any adverse effects like radiation sickness, radiation induced necrosis, normal tissue scarring, etc. Other typical treatment consequences like systemic chemotherapy induced myelo-suppression, loss of appetite and related weight loss, etc are also not experienced during or after the Cytotron therapy.

At Glia Integrated Healthcare, during and after Cytotron therapy, emphasize will be holistic; on emotional, functional and psycho-social well-being of the patients using our well designed Dheergayu Program. Trained onco-counsellors, nutrition experts and the medical team will work together with the patient and their family members to derive more benefits impacted positively by the Cytotron therapy, in order to improve QoL and overall physical well-being of the patient.

Cytotron therapy

Cytotron Therapy

CYTOTRON is a State-of-the-Art Therapeutic Device based on Rotational Field Quantum Magnetic Resonance (RFQMR) which utilizes highly complex electromagnetic beams in the radio frequency spectrum controlled by a computer and guided by MRI.

Cytotron looks like a MRI machine and is the world’s first Rotational Field Quantum Magnetic Resonance (RFQMR) Generator for Tissue Regeneration, Degeneration and Repair for treating several chronic or degenerative diseases such as Cancer & Arthritis. The treatment is non-invasive, painless and free from side effects. Clinical studies have demonstrated that Cytotron is very effective in treating certain conditions such as a damaged knee by regenerating the cartilage tissue or stopping and reversing the growth of a tumor in cancer.

 

Need Any Help?

The breakthrough Cytotron therapy is a new, gentle, safe, Non-invasive treatment intended to stop cancer growth and spreading.

What exactly is Tissue Engineering?

Tissue Engineering is the field of altering, modifying, controlled reproduction and controlled regeneration and degeneration of biological tissue. Using Tissue engineering techniques, today it is possible to regenerate dying tissues and organs inside the body, grow new blood vessels, heal wounds or fix an adamant fracture, grow new cartilage or even teach a few lessons to cancerous cells that go into a multiplication spree.

 

Arresting cell growth with RFQMR

RFQMR technology utilizes a totally different approach compared to conventional cancer treatments. Instead of the very high frequency ionizing radiation used in radiotherapy, RFQMR uses radio or sub-radio frequency, low power, non-ionizing, non-thermal electromagnetic waves.

Manufactured in India, widely accepted Internationally

Cytotron has international patent, manufactured in India, in compliance with ISO 9001:2000 and ISO 13485:2003. It has obtained CE Certificate marking European Conformity for safety, public health and consumer protection and has qualified for CMDCAS, Canada’s Health regulatory requirements making it acceptable in Europe and Canada for tissue regeneration and degeneration.

 

Tissue Regeneration - Osteoarthritis & other Indications

Osteoarthritis (OA) is a pathology which causes severe and long-term pain along with physical disability.

  • It is characterized by a progressive destruction of articular cartilage accompanied by subchondral bone remodeling, osteophyte formation and synovial membrane inflammation

  • This disorder is classified as non-inflammatory arthritis and it is the most common form of arthritis affecting people of all ages, including children

  • So far, no pharmacological treatment exists targeting the mechanisms of OA

  • The underlying etiopathology of OA modulated by fast radio bursts (FRB) is detailed in a recent publication (see Resources)

  • The commonly used treatments principally target symptoms of OA but doesn’t prevent its progression

  • There is an unmet medical need for protecting cartilage degradation, decreasing joint pain and eventually healing joint inflammation as OA progresses from an acute to a chronic state

QMRT is able to re-grow cartilage in the joints, significantly reducing pain, increasing mobility, range of motion and functionality based on International Knee Society Scores and outcome reporting, post QMRT.

Clinically validated Indications of USE with the Cytotron® and QMRT are;

  • Musculo-skeletal (Osteoarthritis of all joints)

  • Musculo-skeletal degeneration (Spinal Dysplasia / Disc Prolapse or Herniated Disc Repair)

Do You Have Any Queries?