Shimada Y
Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Cancer Chemother Pharmacol. 1998;42 Suppl:S80-4. doi: 10.1007/s002800051085.
No standard chemotherapy regimen for the treatment of advanced gastrointestinal cancer exists. However, 5-fluorouracil (5-FU) is being used more frequently as a key component of combination therapy regimens for this disease, and including cisplatin (CDDP) in combination therapy regimens produces significant tumor shrinkage. Although oral formulations of 5-FU are widely used in Japan, their clinical activity and toxicity have not been thoroughly evaluated. In 1992, the Japan Clinical Oncology Group initiated a phase III study in which the survival rates of patients treated with 5-FU 800 mg/m2/day for 5 days by continuous infusion (5-FUci), 5-FUci with CDDP 20 mg/ m2/day for 5 days by infusion, or oral uracil/Ftorafur 375 mg/m2/day with weekly MMC 5 mg/m2 i.v. were compared. This study was closed with 280 patients accrued in 1997, and final analysis was made in early 1998. Irinotecan and paclitaxel are new drugs with activity against gastric cancer. Combination chemotherapy consisting of irinotecan with CDDP has also been evaluated. For treatment of metastatic colorectal cancer, the only active drug previously available in Japan was 5-FU, although 5-FU + leucovorin is the international standard regimen. Irinotecan is now approved in Japan, Europe, and the USA and is the most effective drug for 5-FU-refractory patients. The optimal irinotecan and 5-FU combination regimen is being extensively examined but further trials aimed at accumulating basic data are warranted.
目前尚无用于治疗晚期胃肠道癌的标准化疗方案。然而,5-氟尿嘧啶(5-FU)作为该疾病联合治疗方案的关键组成部分,使用频率越来越高,并且在联合治疗方案中加入顺铂(CDDP)可使肿瘤显著缩小。尽管5-FU的口服制剂在日本广泛使用,但其临床活性和毒性尚未得到充分评估。1992年,日本临床肿瘤学组启动了一项III期研究,比较连续输注5天、剂量为800mg/m²/天的5-FU(5-FUci)、连续输注5天、剂量为800mg/m²/天的5-FU联合剂量为20mg/m²/天的CDDP输注5天,或口服优福定375mg/m²/天联合每周静脉注射丝裂霉素5mg/m²的患者的生存率。该研究于1997年纳入280例患者后结束,并于1998年初进行了最终分析。伊立替康和紫杉醇是对胃癌有活性的新药。伊立替康联合CDDP的联合化疗也已得到评估。对于转移性结直肠癌的治疗,日本此前唯一可用的活性药物是5-FU,尽管5-FU+亚叶酸是国际标准方案。伊立替康现已在日本、欧洲和美国获批,是治疗对5-FU耐药患者最有效的药物。目前正在广泛研究伊立替康与5-FU的最佳联合方案,但仍有必要进行进一步试验以积累基础数据。