In total-body hyperthermia, short-wave infrared radiation penetrates the skin and warms blood vessels close to the surface of the skin. As the temperature rises in the skin and the blood flowing through the skin, the warmth spreads throughout the body, and core temperature begins to increase. Infrared light is one of the primary means used to heat the body in total-body hyperthermia.
As the heat is gradually increased, the patient begins to perspire but without airflow, evaporation cannot occur. Transpiration and perspiration only lead to cooling if the water can be evaporated. Perspiration is our primary means of maintaining stable body temperature. Without this process, body temperature continues to increase, raising core temperature, and inducing a fever-like state. Once the fever is reached and maintained for one to two hours, the heat is very gradually reduced over the course of another hour or two.
In the Gorter Model, directly after total-body hyperthermia treatment, patients receive an injection of Immune restoration vaccine cultured from their own blood. They usually experience mild flu-like symptoms for 6 to 12 hours right after the treatment. This is not the flu—it is the body’s response, which indicates that the immune system is being activated. After these symptoms subside, almost all patients report less pain, and a sense of well-being.
It has been observed that patients who react with flu-like symptoms after the vaccination do clearly better and show more benefit from the therapy than those patients who cannot amount any flu-like symptoms at all. All patients who went in complete remission always experienced flu-like symptoms.
In the past 25 years, more than 1,000 clinical trials and thousands of scientific articles have been published on induced total-body hyperthermia and localized hyperthermia in the peer-reviewed medical literature. Hyperthermia has also been studied for chronic pain, asthma, and other chronic or recurrent respiratory infections, urinary tract infections, and immune deficiency. More than 700 research studies have focused specifically on cancer treatment using total-body hyperthermia. Research on fever therapy for cancer has been performed in medical schools and research centers since the 1980s. These studies have been conducted primarily in the U.S., Germany, and Japan, but also in Australia, China, Denmark, Italy, the Netherlands, New Zealand, Norway, South Korea, and other countries.
Hyperthermia can be used as the primary form of treatment or safely applied in combination with conventional therapies such as chemotherapy or radiation.
American research has been conducted in FDA-approved studies at centers such as the Mayo Clinic, University of Pennsylvania, University of Texas, and Duke University. These studies reflect a global dialogue between researchers across the world that has systematically defined effective fever therapy. Controlled studies have documented that chemotherapy or radiation in combination with total body hyperthermia becomes more effective, often with fewer side effects than chemotherapy or radiation alone. In the European Union, this combination therapy is widely available at numerous major cancer treatment centers in cities such as Amsterdam, Hamburg, Munich, Rotterdam, Stuttgart, and Utrecht.
The approach to fever-range, total-body hyperthermia in the Gorter Model is based on 25 years of clinical experience by Robert Gorter, MD, PhD. The model differs from other treatment protocol in several ways:
Comprehensive therapy — At the Medical Center Cologne, total-body hyperthermia is usually provided in combination with local hyperthermia, injections for Immune restoration, mistletoe injections, and IV nutrients for immune restoration. This therapy enables the immune system to better identify cancer cells and targets efforts to destroy them.
Low intensity — Controlled fever is maintained at a moderate temperature to safe-guard the well-being of the patient. Maximum temperatures range from 38.5 C to 39.5 C.
Carefully-staged treatment — Temperature is gradually increased for three hours and then, after a plateau of about one hour, allowed to return to normal over the course of one to two hours. The average treatment lasts four to six hours in total.
Optimal timing — A major difference with other hyperthermia protocols is the timing sequence. Namely the induced total-body hyperthermia mobilizes the immune system and then the immune system is augmented by the Immune restoration vaccinations. Thus, the body receives millions of its own activated dendritic cells, timed to work together with fever-induced immune system activation.
An absence of side effects — This process involves the body’s innate immune responses. The treatment is accomplished with almost no disruption or side effects — typically less than one day of mild flu-like symptoms at most.
Primary therapy — This timed approach is almost always effective in restarting and enhancing immune function and competence. This method harnesses the biological healing power of fever in the treatment of cancer patients. Once the immune system is engaged, the body begins destroying cancer cells from within. This reduces the need for medication and stabilizes the body against further deterioration. These gains provide the basis for a sense of well-being, improved health, and healing, even in many patients with Stage III and IV (end-stage) cancer.
Complementary to conventional treatment — Fever-range, total-body hyperthermia can be applied as part of a comprehensive immune therapy program or in combination with conventional therapy such as chemotherapy or radiation. The majority of studies have focused on this combination treatment. Research has shown that hyperthermia increases the effectiveness of conventional therapy with fewer side effects than chemotherapy or radiation treatment alone. Also, conventional therapies sustain their efficacy when given in combination with hyperthermia. In the European Union, this type of combination therapy is widely applied in most major cancer treatment centers.
In total body hyperthermia, the patient’s core body temperature is slowly increased to about 102.2° F (39° C) and sometimes even higher to 104° F (40.0° C) if it is medical appropriate.
The immune shift is triggered by an impulse from deep within the brain stem in the hypothalamus. This area of the brain contains the command center for our most basic functions, especially those our bodies carry on without our conscious awareness such as breathing, blood pressure, and core body temperature. This command center guides the autonomic nervous system, which functions “automatically.” Fever is triggered from deep within the most ancient area of the brain, also present in all mammals, which demonstrates how fundamental fever is to our functioning.
Total-body hyperthermia treatment is used to re-launch and activate cells of the immune system. These defenses increase targeted efforts to destroy the cancer through cytotoxicity. This selective toxicity by immune cells targets malignant cells, resulting in tumor cell death (necrosis and apoptosis). Healing occurs as the cancer load is lowered through improved immune activity.
In sum, the fever primes the immune system to destroy cancerous cells and triggers increased immune responses throughout the whole body. I was diagnosed with colon cancer and that spread to my liver. Although I did well on the chemotherapy, the oncologist made it clear that treatment was palliative and not a cure. So we made an appointment for a consultation in Cologne. When we learned that Dr. Gorter’s treatment could be used together with chemotherapy, we decided to do that as well. I began the total body hyperthermia and Immune restoration therapy in Cologne.
Once you’ve received the treatment, you know what to expect. It’s not painful and I was hardly sick at all. I usually feel worse after the Immune restoration vaccination, but only for one day. Every nine weeks a scan is made and they show that there are no new tumors and the liver tumors are getting smaller. The fact that my cancer has stabilized is remarkable. (Truus Kleij-Swan, more than five year long-term survivor of intestinal cancer, metastasized to the liver, lymph nodes and peritoneum.)
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