Suppr超能文献

一项针对晚期结直肠癌患者的每周高剂量持续输注5-氟尿嘧啶联合口服亚叶酸钙的II期试验。西班牙胃肠道肿瘤治疗合作组(TTD)。

A phase II trial of weekly high dose continuous infusion 5-fluorouracil plus oral leucovorin in patients with advanced colorectal cancer. The Spanish Cooperative Group for Gastrointestinal Tumor Therapy (TTD).

作者信息

Aranda E, Cervantes A, Dorta J, Blanco E, Fernández-Martos C, Cruz-Hernandez J J, Carrato A, Gonzalez-Mancha R, García-Conde J, Díaz-Rubio E

机构信息

Hospital Clínico Provincial, Córdoba, Spain.

出版信息

Cancer. 1995 Aug 15;76(4):559-63. doi: 10.1002/1097-0142(19950815)76:4<559::aid-cncr2820760404>3.0.co;2-o.

Abstract

BACKGROUND

In a previous Phase II trial, the authors showed that a weekly continuous infusion of 5-fluorouracil (5-FU) at a dose of 3.5 g/m2 for 48 hours is an active treatment for advanced colorectal cancer. The overall response rate was 38.5%, and the median survival was 12 months. These data were comparable to those achieved by biochemical modulation of 5-FU with leucovorin. To study the modulation of this weekly, high dose, continuous infusion 5-FU with oral leucovorin, a new Phase II trial was planned.

METHODS

From December 1991 to July 1992, 43 previously untreated patients with measurable advanced colorectal cancer were included in a multicenter study. They received on an outpatient basis 5-FU at a weekly dose of 3 g/m2 by continuous infusion for 48 hours until progression or toxicity. Oral leucovorin (60 mg every 6 hours) also was given during the infusion of 5-FU.

RESULTS

Patients received a median dose intensity of 5-FU of 2.2 g/m2/week (range, 0.76-3 g/m2/week). One complete response and 11 partial responses were observed. The overall response rate was 29% (95% confidence interval [CI], 16-45%). Median time to progression was 7 months, and the median survival was 15 months. World Health Organization Grades 3 and 4 diarrhea were observed in 19 (45%) and 6 (14%) patients, respectively. Grade 3 mucositis also was observed in 10 (24%) patients, and Grade 4 mucositis was observed in 1. Grade 3 nausea and vomiting were reported in seven (17%) patients. Grade 3 hand-foot syndrome was detected in only two (2.5%) patients. No leukopenia or thrombocytopenia was observed.

CONCLUSIONS

Oral leucovorin modulation of a weekly 48-hour infusion of 5-FU at a dose of 3 g/m2 of leucovorin is a toxic regimen, always requiring dose reduction, with diarrhea and mucositis as the main limiting toxicities. Its antitumor activity does not seem superior to that observed with a weekly 48-hour infusion of 5-FU alone at a dose of 3.5 g/m2.

摘要

背景

在之前的一项II期试验中,作者表明每周持续输注剂量为3.5 g/m²的5-氟尿嘧啶(5-FU)共48小时是晚期结直肠癌的一种有效治疗方法。总缓解率为38.5%,中位生存期为12个月。这些数据与用亚叶酸对5-FU进行生化调节所取得的数据相当。为了研究口服亚叶酸对这种每周一次的高剂量5-FU持续输注的调节作用,计划开展一项新的II期试验。

方法

从1991年12月至1992年7月,43例既往未接受过治疗的可测量的晚期结直肠癌患者纳入一项多中心研究。他们在门诊接受每周剂量为3 g/m²的5-FU持续输注48小时,直至病情进展或出现毒性反应。在输注5-FU期间还给予口服亚叶酸(每6小时60 mg)。

结果

患者接受的5-FU中位剂量强度为2.2 g/m²/周(范围为0.76 - 3 g/m²/周)。观察到1例完全缓解和11例部分缓解。总缓解率为29%(95%置信区间[CI],16 - 45%)。中位疾病进展时间为7个月,中位生存期为15个月。分别有19例(45%)和6例(14%)患者出现世界卫生组织3级和4级腹泻。10例(24%)患者出现3级黏膜炎,1例出现4级黏膜炎。7例(17%)患者报告有3级恶心和呕吐。仅2例(2.5%)患者检测到3级手足综合征。未观察到白细胞减少或血小板减少。

结论

口服亚叶酸调节每周一次48小时输注剂量为3 g/m²的5-FU是一种毒性方案,总是需要降低剂量,腹泻和黏膜炎是主要的限制毒性。其抗肿瘤活性似乎并不优于每周一次48小时单独输注剂量为3.5 g/m²的5-FU所观察到的活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验