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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Addition of docetaxel to S-1 without platinum prolongs survival of patients with advanced gastric cancer: A randomized study (START)
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Addition of docetaxel to S-1 without platinum prolongs survival of patients with advanced gastric cancer: A randomized study (START)

机译:在没有铂的S-1中添加多西他赛可延长晚期胃癌患者的生存期:一项随机研究(START)

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Purpose: Cisplatin plus 5-fluorouracil has been globally accepted as a standard regimen for the treatment for advanced gastric cancer. However, cisplatin has several disadvantages, including renal toxicity and the need for admission. S-1 plus cisplatin has become a standard treatment for advanced gastric cancer in East Asia. This phase III study was designed to evaluate the potential benefits of adding docetaxel to S-1 without a platinum compound in patients with advanced gastric cancer. Methods: Patients were randomly assigned to receive docetaxel plus S-1 or S-1 alone. The docetaxel plus S-1 group received docetaxel on day 1 and oral S-1 on days 1-14 of a 21-day cycle. The S-1 alone group received oral S-1 on days 1-28 of a 42-day cycle. The primary end point was overall survival. Results: Of the 639 patients enrolled, 635 were eligible for analysis. The median overall survival was 12.5 months in the docetaxel plus S-1 group and 10.8 months in the S-1 alone group (p = 0.032). The median progression-free survival was 5.3 months in the docetaxel plus S-1 group and 4.2 months in the S-1 alone group (p = 0.001). As for adverse events, neutropenia was more frequent in the docetaxel plus S-1 group, but remained manageable. Conclusion: As first-line treatment for advanced gastric cancer, docetaxel plus S-1 significantly improves median overall and progression-free survival as compared with S-1 alone. (ClinicalTrials.gov number: NCT00287768).
机译:目的:顺铂加5-氟尿嘧啶已被全球公认为治疗晚期胃癌的标准方案。但是,顺铂有几个缺点,包括肾毒性和需要入院。 S-1加顺铂已成为东亚晚期胃癌的标准治疗方法。这项III期研究旨在评估在晚期胃癌患者中将多西他赛添加到S-1中而不使用铂类化合物的潜在益处。方法:患者被随机分配接受多西他赛加S-1或S-1。多西他赛加S-1组在21天周期的第1天接受多西他赛,并在第1-14天接受口服S-1。仅S-1组在42天周期的1-28天接受口服S-1。主要终点是总体生存率。结果:在639名患者中,有635名符合分析条件。多西他赛加S-1组的中位总生存期为12.5个月,而单独S-1组的中位总生存期为10.8个月(p = 0.032)。多西他赛加S-1组的中位无进展生存期为5.3个月,而单独的S-1组为4.2个月(p = 0.001)。至于不良事件,多西他赛加S-1组中性粒细胞减少症较常见,但仍可控制。结论:多西他赛加S-1作为晚期胃癌的一线治疗,与单独使用S-1相比,显着提高了中位总体生存率和无进展生存率。 (ClinicalTrials.gov编号:NCT00287768)。

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