首页> 外文期刊>Clinical lung cancer >Results from a single institution phase II trial of concurrent docetaxel/carboplatin/radiotherapy followed by surgical resection and consolidation docetaxel/carboplatin in stage III non-small-cell lung cancer.
【24h】

Results from a single institution phase II trial of concurrent docetaxel/carboplatin/radiotherapy followed by surgical resection and consolidation docetaxel/carboplatin in stage III non-small-cell lung cancer.

机译:多西紫杉醇/卡铂/放疗并发手术切除和巩固多西紫杉醇/卡铂联合治疗第三期非小细胞肺癌的单机构II期试验的结果。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: The optimal treatment of locally advanced non-small-cell lung cancer (NSCLC) remains controversial. We hypothesized that using a trimodality approach in selected patients with stage IIIA/IIIB disease would be both feasible and efficacious with reasonable toxicity. PATIENTS/METHODS: We enrolled 13 patients with resectable stage III NSCLC on a prospective phase II trial of trimodality therapy. Induction treatment consisted of weekly docetaxel 20 mg/m(2) and weekly carboplatin at an area under curve (AUC) of 2 concurrent with 45 Gy thoracic radiotherapy. Resection was performed unless felt to be unsafe or if patients had progressive disease. Postoperative consolidation consisted of docetaxel 75 mg/m(2) and carboplatin at an AUC of 6 every 3 weeks for 3 cycles with growth factor support. RESULTS: All patients responded to induction chemoradiotherapy as measured by total gross tumor volume reductions of 43% on average (range, 27%-64%). Twelve patients underwent resection of the tumor and involved nodes, yielding a resectability rate of 92%. The primary endpoint of 2-year overall survival (OS) was 72% (95% confidence interval [CI], 36%-90%), and 2-year progression-free survival (PFS) was 36% (95% CI, 9%-64%). The maximal toxicity observed per patient was grade II in 5 patients (38%); grade III in 7 patients (54%); grade IV in 1 patient (8%); and grade V in none. CONCLUSION: This trimodality approach resulted in promising outcomes with reasonable toxicity in carefully selected patients with stage III NSCLC at a single institution.
机译:背景:局部晚期非小细胞肺癌(NSCLC)的最佳治疗仍存在争议。我们假设在某些IIIA / IIIB期患者中使用三联疗法将既可行又有效,并具有合理的毒性。患者/方法:我们在一项前瞻性三联疗法II期试验中招募了13例可切除的III期NSCLC患者。诱导治疗包括每周多西他赛20 mg / m(2)和每周卡铂在曲线下面积(AUC)为2的同时进行45 Gy胸腔放疗。除非认为不安全或患者患有进行性疾病,否则应进行切除。术后巩固包括多西他赛75 mg / m(2)和卡铂,每3周6个AUC,连续3个周期,并有生长因子支持。结果:所有患者对诱导放化疗的反应均以总总肿瘤体积平均减少43%(范围为27%-64%)来衡量。 12名患者接受了肿瘤切除并累及淋巴结,可切除率为92%。 2年总生存期(OS)的主要终点是72%(95%置信区间[CI],36%-90%),2年无进展生存期(PFS)是36%(95%CI, 9%-64%)。每位患者观察到的最大毒性为5位患者的II级(38%); 7例患者达到III级(54%); 1名患者达到IV级(8%);没有V级。结论:这种三联疗法方法在单个机构中为精心挑选的III期NSCLC患者带来了可观的结果和合理的毒性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号