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5-氟尿嘧啶、表阿霉素和丝裂霉素C(FEM)联合化疗用于晚期胃癌。由“胃肠道肿瘤化疗组(CGT)”进行的II期试验。

5-Fluorouracil, 4-epidoxorubicin, and mitomycin C (FEM) combination chemotherapy for advanced gastric carcinoma. A phase-II trial by the "chemotherapiegruppe gastrointestinaler tumoren (CGT)".

作者信息

Flechtner H, Queisser W, Heim M E, Henss H, Arnold H, Fritze D, Herrmann R, Fritsch H, Fritz M, Trux F A

出版信息

Onkologie. 1987 Apr;10(2):67-71. doi: 10.1159/000216375.

Abstract

In a phase-II-trial 40 patients with advanced gastric cancer were treated with 5-fluorouracil, 4-epidoxorubicin, mitomycin C (FEM) combination therapy. Twenty-five out of 30 patients with measurable disease were evaluable for response after 8 weeks of treatment. Seven patients achieved a partial remission (PR), suggesting a response rate of 28%. Ten patients had no change (NC) and 8 patients showed progression (P). The median time to progression for patients with PR was 7.2 months and for patients with NC 6.3 months. Median survival time for all patients was 5.3 months, for patients with PR and NC 9.9 months. WHO grade 3 toxicity appeared in 3% (WBC and nausea/vomiting) and 15% (alopecia) of patients. The data suggest that this regimen is not more active, but is better tolerated than the original FAM schedule. Therefore it seems suitable for out-patient treatment, for elderly patients and for those who cannot be treated by more aggressive drugs.

摘要

在一项II期试验中,40例晚期胃癌患者接受了5-氟尿嘧啶、表阿霉素、丝裂霉素C(FEM)联合治疗。30例可测量疾病的患者中有25例在治疗8周后可评估反应。7例患者获得部分缓解(PR),反应率为28%。10例患者病情无变化(NC),8例患者病情进展(P)。PR患者的中位进展时间为7.2个月,NC患者为6.3个月。所有患者的中位生存时间为5.3个月,PR和NC患者为9.9个月。3%的患者出现世界卫生组织3级毒性(白细胞减少和恶心/呕吐),15%的患者出现脱发。数据表明,该方案活性并不更高,但耐受性优于原FAM方案。因此,它似乎适合门诊治疗、老年患者以及那些不能用更强效药物治疗的患者。

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