首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Cisplatin plus gemcitabine with or without vinorelbine as induction chemotherapy prior to radical locoregional treatment for patients with stage III non-small-cell lung cancer (NSCLC): results of a prospective randomized study.
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Cisplatin plus gemcitabine with or without vinorelbine as induction chemotherapy prior to radical locoregional treatment for patients with stage III non-small-cell lung cancer (NSCLC): results of a prospective randomized study.

机译:顺铂联合吉西他滨联合或不联合长春瑞滨作为局部Ⅲ期非小细胞肺癌(NSCLC)患者根治性局部治疗前的诱导化疗:一项前瞻性随机研究的结果。

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摘要

To evaluate possible improvement in objective response of adding vinorelbine (V) to the combination of cisplatin/gemcitabine (CG) in induction chemotherapy for stage III NSCLC, patients (n=154) aged < or =75 years, Karnofsky index > or =70%, were stratified by stage (IIIA versus IIIB) and randomly assigned to receive: C (50mg/m(2) i.v.) plus G (1250mg/m(2) i.v.) or CG plus V (25mg/m(2) i.v.). All drugs were administered on days 1 and 8 of an every 3-week cycle. At conclusion, local treatment (LT) with surgery and/or radiotherapy was scheduled. The results indicated that, following a median of 3 cycles, the overall efficacy was 65% in the CG and 61% in the CGV group. Most patients in both groups received radiotherapy as part of their LT. Pathological complete response was confirmed by surgery in 18% in the CG and 25% in the CGV group. Median progression-free survival was 368 days in the CG and 322 days in the CGV group. There were no statistically significant differences in toxicities between groups. Weconclude that the CG and CGV combinations had similar efficacy and moderate toxicity, without accruing to the triplet combination.
机译:为了评估III期NSCLC诱导化疗中长春瑞滨(V)与顺铂/吉西他滨(CG)联合使用对客观反应的可能改善,年龄≥75岁,年龄≥75岁,Karnofsky指数≥70的患者(n = 154) %,按阶段(IIIA与IIIB)分层,并随机分配为接受:C(50mg / m(2)iv)加G(1250mg / m(2)iv)或CG加V(25mg / m(2)iv )。每3周一次的第1天和第8天使用所有药物。最后,计划了手术和/或放疗的局部治疗(LT)。结果表明,经过3个周期的中位数,CG的总体疗效为65%,CGV组的总体疗效为61%。两组中的大多数患者都接受了放疗作为其LT的一部分。手术证实,CG的病理完全缓解率为18%,CGV组为25%。 CG的中位无进展生存期为368天,CGV组的中位无进展生存期为322天。两组之间的毒性没有统计学上的显着差异。我们认为CG和CGV组合具有相似的疗效和中度毒性,但不涉及三联体组合。

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