The Cause and Treatment of Cancer
The NSW State Cancer Council supports the orthodox view that cancer is a localised condition caused only by physiological conditions. The alternative point of view, however, sees cancer as a late-stage symptom of an underlying systemic disease that affects the whole body. Which theory is correct and why?
Different theories about the cause and treatment of cancer
The NSW State Cancer Council supports the orthodox approach to the treatment
of cancer. Essentially this means that a small malignant tumour is an
early, localised stage of cancer which, if detected early enough and completely
removed, can be cured. Once cancer has metastasised (spread) it is no
longer curable. Cancer is considered caused by only physiological factors.
The alternative approach to the treatment of cancer sees the small malignant
tumour as a late-stage symptom of an underlying systemic disease affecting
the whole body. It sees cancer as being caused by physiological, psychological
and spiritual factors. As a result of these factors several bodily systems
break down (degenerate). The cells mitochondria become depleted in energy;
cells can no longer dispose of waste products; the various immune defence
factors such as natural killer cells, macrophages and lymphocytes become
fewer in number and less active in their function. This situation leads
to tumour formation. This can therefore only be reversed by seeking out
the causes of degeneration in these three areas.
Surgery and radiotherapy are normally seen as ineffective treatments
because they are dealing with symptoms, not the cause. Chemotherapy, although
it is normally a systemic therapy, is in most cases seen as doing serious
damage to the body s natural defence systems and therefore unlikely to
have any long-term benefits. Alternative treatments that are based on
restoring and strengthening the body s own healing mechanisms rather than
harming them are therefore seen as more likely to be effective in controlling
The Efficacy of Orthodox Treatments
The only scientifically acceptable method of assessing the efficacy of
a cancer treatment is the randomised trial. This involves comparing survival
or mortality between a treated group and a control group. Patients are
allocated to these groups at random. Available evidence shows that neither
surgery nor radiotherapy has been proven in a randomised trial to be effective
in controlling cancer either by improving survival or reducing mortality.
Radiotherapy can reduce recurrence significantly but without affecting
overall survival. Chemotherapy has been shown in randomised trials to
be effective in increasing survival by a few weeks or months only in one
type of solid tumour – small-cell lung cancer. In view of the serious
side-effects experienced, even this treatment must also remain questionable.
Comparison of survival.
Indirect evidence such as comparison of percentage 5-year survival over
time is not reliable. Factors unrelated to treatment can have a significant
effect on survival figures (1). Most observed apparent increases in survival
are normally due to earlier diagnosis and do not affect time of death.
Unless the increased survival is very large and the effects of increased
incidence and earlier diagnosis have been eliminated or allowed for, claims
of improved survival must be seriously questioned. Comparison of incidence
and mortality over time is a better measure of improved survival(1). Such
comparisons show that no increased survival can be attributed to intervention
with surgery or radiotherapy(2). Chemotherapy has been shown to produce
a significant increase in survival in a particular type of acute childhood
leukemia and some lymphomas. Claimed improvements in survival in other
areas have been significantly overstated(3).
Tumour response studies
Tumour response studies used to prove the efficacy of chemotherapy are
invalid since there has been no correlation demonstrated between improved
response (tumour shrinkage) and improved survival(4). This suggests that
the orthodox theory of cancer, that the tumour is the disease, is invalid.
Any treatment capable of removing or shrinking a tumour that is threatening
a vital organ, such as a tumour obstructing the bowel or pressing on the
brain, can extend life, but this can be done without affecting the disease
itself. These tests for efficacy show that orthodox therapies are effective
for only about 6% of cancer cases. This is not surprising in view of the
fact that there is scientific backing for only 15% of all medical interventions(5)
and cancer is considered to be more difficult to treat than most other
The same lack of evidence for efficacy exists in the area of cancer screening.
This applies to screening for cancer of the uterus using the PAP smear;
for cancer of the breast using mammograms; for colorectal cancer; and
for prostate cancer. In none of these areas is there reliable evidence
that widespread screening over many years has had any effect on mortality
from these diseases. For example reduction in mortality observed in some
randomised mammogram screening trials can be explained by poor methodology
rather than earlier intervention following earlier diagnosis(6).
The Efficacy of Alternative Treatments
Very few alternative cancer treatment have been subjected to a randomised
trial that has shown extended survival. One is psychotherapy. Median Survival
was almost doubled from 19 months to 37 months following this additional
treatment(7). This is consistent with the systemic theory of cancer that
holds that psychological factors can play a significant part in the breakdown
of the body s metabolic and immune functions. It is not consistent with
the orthodox (localised) theory of cancer that sees only physiological
factors involved in the cause and control of cancer.
Comparison of survival
Using indirect evidence such as from an unmatched comparison of survival
of advanced stage cancer patients after conventional treatment followed
by an alternative treatment with survival after conventional treatment
alone suggests that there are other alternative cancer treatments that
appear to produce a significant extension of survival. These include:
Whole-Body Therapy developed by Dr Josef Issels in Bavaria, Germany(8) –
This produced 16.6% 5-year survival with terminal cancer patients compared
with <5% expected from orthodox treatments; and 15% 15-year survival compared
with <2% expected from orthodox treatments. A second therapy that has been
tested in clinical trials is Hydrazine Sulphate, developed by Dr Joseph
Gold in New York(9). Scientists in Russia have confirmed that it stops cachexia
(cancer-induced starvation in 50% of cases, shrinks inoperable malignant
and non-malignant brain tumours, and also produces a significant improvement
in survival in lymphomas, particularly Hodgkin s disease. A third therapy
currently undergoing a clinical trial is shark cartilage. Preliminary results
suggest some effect of treatment on survival(10).
Such trials of alternative therapies are normally only permitted with
patients with advanced cancer. This is on the grounds that patients must
first be treated with the “proven” therapies of surgery, radiotherapy
In addition to these there are over 100 different therapies for which
there is either scientific evidence of effect on tumours or anecdotal
evidence of unexpected long-term remission (11,12). Many of these have
been investigated by the US Congress, Office of Technology Assessment(13).
Some have subsequently been referred to the US National Institutes of
Health s Office of Alternative Medicine for proper evaluation.
The concept of spontaneous remission is not consistent with the orthodox
theory of cancer because it is widely believed that once a tumour reaches
a palpable size the body s immune system is not capable of destroying
it or controlling its growth. It is however consistent with the systemic
theory of cancer since anything that can reverse the cancer process in
the body is likely to result in the tumour disappearing in due course
or becoming inactive.
|Dr Lawrence BURTON||Immuno-Augmentative-Therapy||Freeport, Bahamas*|
|Dr Stanislaw BURZYNSKI||Antineoplastons||Houston, Texas*|
|Dr Donald COLE||Hyperthermia||New York *|
|Dr William COLEY||Coley’s Toxins||Tijuana, Mexico*|
|Dr Kurt DONSBACH||D.M.S.O.+ Hydrogen peroxide||Tijuana, Mexico*|
|Dr Max GERSON||Gerson Diet||US*|
|Dr Joseph GOLD||Hydrazine Sulphate||Tijuana, Mexico*|
|Mr Harry HOXSEY||Hoxsey Herbal Tonic||US*|
|Dr William KELLEY||Kelley Diet||US|
|Dr William KOCH||Glyoxylide||US and Japan*|
|Dr Ishio KUSHI||Macrobiotic Diet||US and Mexico|
|Dr William LANE||Shark Cartilage||Switzerland*|
|Dr Anita LEROI||Iscador||US|
|Dr Robert LINCOLN||Bacteriophage Method||San Diego, Calif.*|
|Dr Virginia LIVINGSTON||Cancer Vaccine||Tijuana, Mexico|
|Dr Harold MANNER||Vitamins A,C,E and Amygdalin||Quebec, Canada|
|Dr Gaston NAESSENS||714X||California*|
|Dr Linus PAULING||Vitamin C megadoses||New York*|
|Dr Emanuel REVICI||Non-toxic Chemotherapy||San Diego, Calif.|
|Dr David RUBIN||D.M.B.G.||Pacif. Palis., CA*|
|Dr Carl SIMONTON||Psychotherapy|
|Ann WIGMORE||Wheatgrass Diet||Boston and Florida*|
*These therapies were investigated by the US Congress, Office of Technology
Assessment (see US Congress, Office of Technology Assessment, Unconventional
Cancer Treatments, OTA-H-405, Washington DC: US Government Printing Office,
- Enstrom, JE and Austin, DF. Interpreting Cancer Survival Rates. Science
1977: 195; 847-851.
- Benjamin, DJ. The Efficacy of Surgical Treatment of Cancer. Medical Hypotheses
1993: 40; 129-138.
- US Congress General Accounting Office. Cancer patients survival: what progress
has been made? PEMD-87-13, (3/31/87).
- Moss, R. Questioning Chemotherapy. New York: Equinox Press, 1995.
- Editorial, Where is the wisdom…? – The poverty of medical evidence. BMJ
1991: 303: 798-99.
- Benjamin, DJ. The efficacy of surgical treatment of breast cancer. Proceedings
of The Lancet Conference: “The challenge of breast cancer”; 1994 21-22 April;
Brugge, Belgium; Medical Hypotheses 1996; 47 (5): 389-97.
- Spiegel, D. et al. Effect of psychosocial treatment on survival of patients
with metastatic breast cancer. The Lancet, October 14 1989; 888-891.
- Issels, J. Immunotherapy in Progressive Metastatic Cancer – Fifteen-Year
Follow-Up. Clinical Trials Journal August 1990: 357-365.
- Gold, J. Article by Jeff Kamen: From Russia With Love … Stonewalled in
the U.S.A., Penthouse
- Lane, IW, Shark Cartilage
- Moss, RW. Cancer Therapy, New York: Equinox Press, 1992.
- Pelton, R and Overholser, L. Alternatives in Cancer Therapy. New York: Simon
& Schuster, 1994.
- US Congress, Office of Technology Assessment, Unconventional Cancer Treat-ments,
OTA-H-405, Washington DC: US Government Printing Office, September 1990.