Gemcitabins (Gemzar) is a nucleoside analog increasingly used in the treatm
ent of a variety of solid tumors. DNA synthesis is inhibited by gemcitabine
by masked chain termination and via inhibition of ribonucleotide reductase
. Synergy may exist between gemcitabine and other antimetabolites, includin
g 5-fluorouracil. The varying patterns of dose-limiting toxicities to gemci
tabine and UFT (uracil and tegafur in a 4:1 molar ratio) plus oral calcium
folinate (Orzel) permit their use in combination. The primary aint of this
phase I study is to determine the maximum tolerated doses of gemcitabine an
d UFT plus oral calcium folinate irt patients with a variety of solid tumor
s. Only eight patients have been recruited to date,,vith myelosuppression b
eing the main toxicity observed.