Maehara Y, Sugimachi K, Kurihara M, Taguchi T
Department of Surgery II, Kyushu University School of Medicine, Fukuoka, Japan.
Gan To Kagaku Ryoho. 1999 Mar;26(4):476-85.
In developing a new anticancer agent, it is most important to balance the antitumor activity and toxicity of the agent. S-1 was designed to achieve high activity and low toxicity. In it tegafur, a prodrug of 5-FU, is combined with two classes of modulators. CDHP, an inhibitor of 5-FU degradation in the liver, and Oxo, an inhibitor of 5-FU phosphoribosylation in the digestive tract. In both early and late Phase II studies, S-1 was effective against advanced or recurrent gastrointestinal cancer. Toxicities were generally mild, and there were no toxic deaths.