We review the pharmacology and clinical administration of the commonly used
platinum-based anticancer drugs cisplatin and carboplatin, and the more re
cently approved diamminocyclohexane-based oxaliplatin. The development of a
nalogues of cisplatin has been focused upon identifying compounds with less
toxicity and with a different spectrum of activity.
Carboplatin exemplifies the former, while the initial data with oxaliplatin
support its activity in cisplatin-resistant tumours. The clinical pharmaco
kinetics of the drugs are reviewed. Incorporation of these data into the de
sign of clinical regimens has permitted individualised therapy with carbopl
atin, and has enhanced safety. Additional investigation of the pharmacodyna
mics of all of these agents is expected to result in their selective applic
ation. The clinical effects of these analogues are discussed.