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顺铂联合吉西他滨加或不加长春瑞滨作为 III 期非小细胞肺癌(NSCLC)患者根治性局部区域治疗前的诱导化疗:一项前瞻性随机研究的结果

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.

作者信息

Esteban Emilio, de Sande Jose-Luis, Villanueva Noemi, Corral Norberto, Muñiz Isabel, Vieitez José M A, Fra Joaquin, Fernández Yolanda, Estrada Enrique, Fernandez José-Luis, Luque Maria, Jimenez Paula, Mareque Beatriz, Capellan Marta, Buesa José M A, Lacave Angel Jimenez

机构信息

Servicio de Oncología Médica, Hospital Central de Asturias, Julián Clavería s/n, 33006 Oviedo, Asturias, Spain.

出版信息

Lung Cancer. 2007 Feb;55(2):173-80. doi: 10.1016/j.lungcan.2006.09.021. Epub 2006 Oct 27.

Abstract

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. We conclude that the CG and CGV combinations had similar efficacy and moderate toxicity, without accruing to the triplet combination.

摘要

为评估在 III 期非小细胞肺癌诱导化疗中,在顺铂/吉西他滨(CG)方案基础上加用长春瑞滨(V)是否能改善客观缓解率,将年龄≤75 岁、卡诺夫斯基指数≥70%的 154 例患者按分期(IIIA 期与 IIIB 期)分层,随机分配接受:C(50mg/m²静脉注射)加 G(1250mg/m²静脉注射)或 CG 加 V(25mg/m²静脉注射)。所有药物均在每 3 周周期的第 1 天和第 8 天给药。疗程结束时,安排进行手术和/或放疗的局部治疗(LT)。结果表明,经过中位 3 个周期治疗后,CG 组的总有效率为 65%,CGV 组为 61%。两组中大多数患者接受放疗作为其 LT 的一部分。CG 组 18%的患者经手术证实为病理完全缓解,CGV 组为 25%。CG 组的中位无进展生存期为 368 天,CGV 组为 322 天。两组之间的毒性无统计学显著差异。我们得出结论,CG 和 CGV 联合方案具有相似的疗效和中度毒性,不支持三联方案。

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