Oxaliplatin (Eloxatin(TM)), a recently developed third-generation cisplatin
analogue with a 1,2-diaminocyclohexane (DACH) carrier ligand, has displaye
d preclinical and clinical activity in a wide variety of tumour types. Syne
rgistic with 5-FU in colorectal cancer (CRC), the combination has proven ef
ficacy in 5-FU-resistant advanced disease and in previously untreated CRC,
as demonstrated in controlled phase III trials, while evaluation in the adj
uvant setting is ongoing. Due to its excellent safety profile, its unique m
echanism of action and lack of cross-resistance with other active agents in
CRC, oxaliplatin has also been combined with CPT-II and Raltitrexed with p
romising results. Trials in pretreated and untreated advanced ovarian cance
r (AOC), as a single agent or in combination with cisplatin, cyclophosphami
de or paclitaxel, indicate a yet to be defined role in AOC and confirm its
lack of cross-resistance with cis/carboplatin. Clinical investigations of s
ingle agent and combination therapies in breast, lung, prostate and germ-ce
ll carcinomas, non-Hodgkin's lymphoma and malignant mesothelioma are being
pursued. While the role of oxaliplatin in medical oncology is yet to be ful
ly defined, it appears to be an important new anticancer agent. (C) 2000 El
sevier Science Ireland Ltd. All rights reserved.