Major advances in cellular biology, genetics, pharmacology and immunology i
n the past decade are beginning to be translated into progress in cancer tr
eatment. This progress is manifested by new cytotoxic drugs which have rece
ntly entered clinical practice (taxanes, topoisomerase I inhibitors, gemcit
abine, vinorelbine, new purines), as well as the efficacy of monoclonal ant
ibody therapies against the CD-20 antigen of B-cell lymphomas and the Her2/
neu oncogene in breast cancer. Several new drugs in development are targete
d at reversal or prevention of the multidrug resistance mechanism caused by
expression of the MDR1 gene (P-glycoprotein). Tumour angiogenesis as a tar
get is being studied in several early clinical trials. As with many other b
iological therapies, the evaluation of these compounds and their integratio
n with standard therapies presents a major challenge to clinical investigat
ors. The emerging field of genomics and gene expression microarrays will pr
ovide enormous information about the biology of cancers. This technology of
fers great opportunities for the discovery of new therapeutic targets, whic
h should provide a basis for the design and evaluation of many new agents i
n the coming decade.