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Possible pills for cancer - and how they work
The figure for cure rates for cancer in adults has improved year on year for the last 14
years. On average 5,000 fewer people have been dying of cancer each year since 1990.
There has been a 12-14% increase in cure rates in breast cancer whilst children's cancer treatment
is increasingly successful.
Breakthrough treatments have been in rare cancers such as testicular cancer, childhood leukaemia,
Hodgkin's disease and lymphoma. But cancer researchers anticipate that within 10 to 15 years
new drugs, based on molecular biology, should be available that will tackle all the big cancers -
lung, breast, colon and prostate.
Cell killing
One promising line of research is into ADEPT, an acronym for antibody-directed enzyme pro-drug
therapy. This is a two stage therapy. In the first stage, the patient is injected with
antibodies which have the characteristic that they bind onto cancer cells. The antibodies
have an enzyme attached to them as it were piggy backed on the antibody. A few days later
comes stage two, in which the patient is injected with a toxic cancer drug. This toxic drug
is activated by the enzyme which is already on the cancer cells but not attached to healthy
cells. The idea is that the cancer cells are killed in a matter of minutes leaving the
healthy cells alone. ADEPT has been worked on for the past eleven years and clinical studies
have just started at the Royal Free Hospital, London.
Starvation
Another line of research about which many experts are enthusiastic is vascular targeting.
Tumour cells like other cells cannot multiply without a blood supply. In aggressive tumours
blood vessels grow rapidly and chaotically. Now, drugs have been developed which aim to cut
off the blood supply to tumours, causing vascular shutdown and so shrinking them to a manageable
size.
Gene therapy
Destroying cancer cells through gene therapy is yet another promising approach. Dr Ros Eeles
and Dr David Dearnaley, at the Institute of Cancer Research in Surrey have undertaken a nationwide
search for prostate cancer genes. The project will be examining the DNA of large numbers of
men. To deal with the volume of results, Prostate Research Campaign UK has helped finance a
new gene sequencer which can analyse DNA samples 36 times faster than earlier equipment.
The team at the Sutton based institute has already been responsible for discovering an important
breast cancer gene, BRCA2. For prostate cancer Dr Eeles is looking for two kinds of gene - a
high risk gene which is likely to show up from the study of families with a history of prostate
cancer and a low risk gene which is likely to be more prevalent in the general population.
If the genes are found, it opens up the prospect of screening to detect those at high risk..
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