Sato A, Hasegawa K, Kurihara M, Takahashi M, Akazawa S, Fukuyama Y, Koizumi W, Hayakawa M, Sasai T, Kimura K
Dept. of Internal Medicine, Jizankai Medical Foundation, Tsuboi Cancer Center Hospital.
Gan To Kagaku Ryoho. 1995 Sep;22(10):1355-62.
An early phase II study of tegafur-uracil (UFT) combined with cisplatin (CDDP) was conducted in patients with advanced gastric cancer. UFT was administered orally for 28 consecutive days at a dose of 400 mg/m2 and CDDP was injected intravenously for 3 day at a dose of 30 mg/m2 over 8 hours every 4 weeks. This treatment cycle was repeated every 4 weeks. Sixteen patients were enrolled in this study and 14 patients could be evaluated for clinical response and toxicity. Based on the results of extramural review, 6 of 14 patients achieved a partial response and the response rate was 42.9%. High grade toxicities (WHO grade 3 or 4), specifically anorexia, nausea and vomiting, diarrhea, and leukocytopenia, were seen in 5, 2, 3 and 2 patients, respectively. The overall median survival time was 347 days (11.4 months) for evaluated patients. Although these results are preliminary, this regimen does appear to be effective in terms of tumor response and survival. Larger patient numbers in a Phase II study and further studies to evaluate survival are awaited.
开展了一项替加氟-尿嘧啶(UFT)联合顺铂(CDDP)用于晚期胃癌患者的II期早期研究。UFT连续28天口服给药,剂量为400mg/m²,CDDP每4周静脉注射3天,剂量为30mg/m²,每8小时一次。此治疗周期每4周重复一次。16例患者入组本研究,14例患者可进行临床反应和毒性评估。根据外部评审结果,14例患者中有6例获得部分缓解,缓解率为42.9%。5例、2例、3例和2例患者分别出现了高级别毒性(WHO 3级或4级),具体为厌食、恶心和呕吐、腹泻以及白细胞减少。评估患者的总中位生存时间为347天(11.4个月)。尽管这些结果是初步的,但该方案在肿瘤反应和生存方面似乎确实有效。期待在II期研究中纳入更多患者,并开展进一步研究以评估生存情况。