It has been 50 years since the first anticancer drug of the modern era, nitrogen mustard, underwent clinical trial in a cancer patient [1]. Nitrogen mustard was introduced into general clinical practice in 1949. Since that time there has been a steady increase in the number of anticancer drugs so that in the U.S.A. there are now 45 officially approved anticancer drugs excluding steroidal agents and radiopharmaceuticals [2]. Despite this large number of drugs the early hope that chemotherapy would provide a major check against cancer has not been realised. Today, chemotherapy is curative for about 12% of human cancers, including choriocarcinoma, acute lymphocytic leukaemia, Hodgkin's disease and testicular cancer. However, most human cancers, those causing over 75% of cancer deaths including lung, colon, breast and prostate cancer, are refractory to chemotherapy. Survival rates for cancer patients in the U.S.A. are about 50%, compared to 40% in the early 1960s, before the widespread use of chemotherapy [3]. There is clearly a need for new treatments and approaches to dealing with cancer and this includes new types of cancer drugs.
CITATION STYLE
Powis, G. (1994). Pharmacological Intervention with Signal Transduction. In New Approaches in Cancer Pharmacology: Drug Design and Development (pp. 39–54). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-642-79088-1_5
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