Cellular responses to anti-cancer agents result from the interaction betwee
n drugs, cellular targets and mechanisms of damage repair. Despite the phar
macological advances in the treatment of cancer, the clinical efficacy of c
hemotherapy is unpredictable in most patients. However, new information on
the genetics of cancer delineates strategies by which the genetic backgroun
d of tumour cells and patients might be profiled to select anti-cancer agen
ts with improved efficacy and tolerability. This article focuses on the app
lication of pharmacogenetics in the characterization of differences in the
pharmacokinetics and pharmacodynamics of anti-cancer agents among individua
ls to define the likelihood of response and reduce the incidence of adverse
effects.