Colorectal cancer remains the second most common cause of cancer death in E
urope. A number of new agents, with varying mechanisms of action, have been
developed and are being evaluated, both as single agents and in combinatio
n. Irinotecan, a topisomerase I inhibitor, and oxaliplatin, a new platinum
compound, have proven efficacy in advanced colorectal cancer resistant to 5
-fluorouracil, Capecitabine and other oral fluoro-pyrimidines are also emer
ging as potentially effective drugs. Raltitrexed and other inhibitors of th
ymidylate synthase (TS) are entering clinical practice although their role
has yet to be determined. The new fluoro-pyrimidines and TS inhibitors are
important classes of drug which have been designed to take advantage of the
knowledge of folate metabolism gained from basic clinical research. Their
design features could perhaps reduce the toxicity seen with the first gener
ation cytotoxic agents. This review will focus on these new chemotherapeuti
c agents in colorectal cancer with respect to their mechanisms of action, c
urrent clinical activity and their potential use both in the adjuvant and p
alliative settings.