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首页> 外文期刊>Japanese journal of clinical oncology. >A multicenter phase-II study of 5-FU, leucovorin and oxaliplatin (FOLFOX6) in patients with pretreated metastatic colorectal cancer.
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A multicenter phase-II study of 5-FU, leucovorin and oxaliplatin (FOLFOX6) in patients with pretreated metastatic colorectal cancer.

机译:多中心II期研究了5-FU,亚叶酸钙和奥沙利铂(FOLFOX6)在转移性结直肠癌治疗前患者中的作用。

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OBJECTIVE: Infusional 5-fluorouracil and leucovorin with oxaliplatin is one of the standard regimens for patients with pretreated metastatic colorectal cancer, as well as for first-line chemotherapy. FOLFOX4 has shown its efficacy in pivotal trials, but patients must make twice-weekly hospital visits. FOLFOX6 is a more convenient regimen, requiring a visit once every two weeks. The objective of this study was to evaluate the efficacy and safety profile of FOLFOX6 in Japanese patients with pretreated colorectal cancer. METHOD: Fifty-one metastatic colorectal cancer patients who failed to respond to first-line chemotherapy were enrolled in the study from April to July 2005. Oxaliplatin, 5-fluorouracil and l-leucovorin were administered every two weeks. Oxaliplatin (100 mg/m(2)) and l-leucovorin (200 mg/m(2)) were given intravenously over 2 h followed by 5-fluorouracil bolus 400 mg/m(2) i.v. and 46-h infusion of 2400 mg/m(2). The primary endpoint was the response rate. RESULTS: Two patients had no measurable lesions and were excluded from the efficacy analysis. Of the 49 eligible patients, one complete response and 6 partial responses were observed, resulting in a response rate (RR) of 14.3% (95% confidence interval: 5.9-27.2%). Median time to treatment failure and progression-free survival was 4.4 and 5.3 months, respectively. Overall survival was 11.4 months. The incidence of grade 2/3 (Debiopharm neurotoxicity criteria) peripheral neuropathy was 41.2%, whereas the overall incidence of grade 3/4 neutropenia was 43.2%. CONCLUSION: The results of our study suggest that FOLFOX6 had an acceptable profile in terms of both efficacy and safety in previously treated colorectal cancer patients.
机译:目的:输注5-氟尿嘧啶和亚叶酸钙与奥沙利铂是治疗转移性结直肠癌的患者以及一线化疗的标准方案之一。 FOLFOX4在关键试验中已显示出功效,但患者必须每周两次就诊。 FOLFOX6是一种更方便的治疗方案,需要每两周拜访一次。这项研究的目的是评估FOLFOX6在日本大肠癌预治疗患者中的疗效和安全性。方法:2005年4月至2005年7月,对51例对一线化疗无效的转移性结直肠癌患者进行了研究。每两周给药一次奥沙利铂,5-氟尿嘧啶和l-亚叶酸。在2小时内静脉内注射奥沙利铂(100 mg / m(2))和l-亚叶酸(200 mg / m(2)),然后静脉注射5-氟尿嘧啶400 mg / m(2)。和46小时输注2400 mg / m(2)。主要终点是缓解率。结果:两名患者没有可测量的病变,被排除在疗效分析之外。在这49名合格患者中,观察到1例完全缓解和6例局部缓解,缓解率(RR)为14.3%(95%置信区间:5.9-27.2%)。治疗失败和无进展生存的中位时间分别为4.4和5.3个月。总生存时间为11.4个月。 2/3级(Debiopharm神经毒性标准)周围神经病变的发生率为41.2%,而3/4级中性粒细胞减少的总发生率为43.2%。结论:我们的研究结果表明,FOLFOX6在先前接受治疗的大肠癌患者的疗效和安全性方面均可接受。

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