Advanced gastric carcinoma remains an incurable disease with a median
survival of 6 to 9 months, and available therapeutic approaches are pr
edominantly palliative. In small controlled trials, systemic chemother
apy has improved survival and quality of life of patients with advance
d gastric carcinoma when compared with best supportive care. Patients
with good performance status (Zubrod less than or equal to 2), low tum
or bulk, and good organ function ape most likely to benefit from chemo
therapy or combined-modality therapy. There is no generally accepted s
tandard chemotherapy for advanced gastric carcinoma. Fluorouracil- and
/or cisplatin-based combinations are often employed. Recently, several
new classes of drugs have demonstrated activity against advanced dise
ase. These include the taxanes (paclitaxel [Taxol] and docetaxel [Taxo
tere], camptothecins (irinotecan [Camptosar]), and fluorouracil prodru
gs (second- and third-generation agents, such as UFT [uracil and tegaf
ur] and S-1). Early results with either single-agent therapy or combin
ations of new agent (irinotecan, paclitaxel, and docetaxel) and more c
onventional agents (cisplatin [Platinol] and fluorouracil) are encoura
ging. Several of these results need to be confirmed and eventually stu
died in well-designed, phase III trials. Similarly, a number of new co
mbinations may be used in the future as preoperative therapies for gas
tric carcinoma. Nearly all of the new agents have radiosensitizing pro
perties. This affords another opportunity to investigate new chemother
apeutic agents in conjunction with radiation therapy in patients with
locoregional gastric carcinoma.