...
首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Randomized Phase II Trial of Carboplatin–Paclitaxel Compared with Carboplatin–Paclitaxel–Trastuzumab in Advanced (Stage III–IV) or Recurrent Uterine Serous Carcinomas that Overexpress Her2/Neu (NCT01367002): Updated Overall Survival Analysis
【24h】

Randomized Phase II Trial of Carboplatin–Paclitaxel Compared with Carboplatin–Paclitaxel–Trastuzumab in Advanced (Stage III–IV) or Recurrent Uterine Serous Carcinomas that Overexpress Her2/Neu (NCT01367002): Updated Overall Survival Analysis

机译:Carboplatin-PAClitaxel的随机期II试验与晚期(IIII-IV)或经复制的子宫浆液癌的Carboplatin-PACLitaxel-Trastuzumab(NCT01367002):更新总存活分析

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: Uterine-serous-carcinoma (USC) is an aggressive variant of endometrial cancer. On the basis of preliminary results of a multicenter, randomized phase II trial, trastuzumab (T), a humanized-mAb targeting Her2/Neu, in combination with carboplatin/paclitaxel (C/P), is recognized as an alternative in treating advanced/recurrent HER2/Neu-positive USC. We report the updated survival analysis of NCT01367002. Patients and Methods: Eligible patients had stage III to IV or recurrent disease. Participants were randomized 1:1 to receive C/P for six cycles ± T followed by maintenance T until progression or toxicity. Progression-free survival (PFS) was the primary endpoint; overall survival (OS) and toxicity were secondary endpoints. Results: Sixty-one patients were randomized. After a median-follow-up of 25.9 months, 43 progressions and 38 deaths occurred among 58 evaluable patients. Updated median-PFS continued to favor the T-arm, with medians of 8.0 months versus 12.9 months in the control and T-arms (HR = 0.46; 90% CI, 0.28–0.76; P = 0.005). Median-PFS was 9.3 months versus 17.7 months among 41 patients with stage III to IV disease undergoing primary treatment (HR = 0.44; 90% CI, 0.23–0.83; P = 0.015), and 7.0 months versus 9.2 months among 17 patients with recurrent disease (HR = 0.12; 90% CI, 0.03–0.48; P = 0.004). OS was higher in the T compared with the control arm, with medians of 29.6 months versus 24.4 months (HR = 0.58; 90% CI, 0.34–0.99; P = 0.046). The benefit was most notable in those with stage III to IV disease, with survival median not reached in the T-arm versus 24.4 months in the control arm (HR = 0.49; 90% CI, 0.25–0.97; P = 0.041). Toxicity was not different between arms. Conclusions: Addition of T to C/P increased PFS and OS in women with advanced/recurrent HER2/Neu-positive USC, with the greatest benefit seen for the treatment of stage III to IV disease.
机译:目的:子宫内癌(USC)是子宫内膜癌的侵略性变体。在多中心的初步结果的基础上,随机分子II试验,靶向HER2 / NEU的人源化MAb,与Carboplatin /紫杉醇(C / P)组合,被认为是治疗先进/的替代方案复发性HER2 / NEU-阳宇。我们报告了NCT01367002的更新存活分析。患者和方法:符合条件的患者患有III阶段至IV或复发性疾病。参与者随机1:1接收C / P六个循环±T,然后进行维护T直到进展或毒性。无进展生存期(PFS)是主要终点;总生存(OS)和毒性是次要终点。结果:六十一名患者随机。在25.9个月的中位随访后,58名可评估患者中发生了43例进展和38人死亡。更新的中位数-PFS继续支持T形臂,中位数为8.0个月,对照和T形臂12.9个月(HR = 0.46; 90%CI,0.28-0.76; P = 0.005)。中位数-PFS为9.3个月,41例患有初级治疗的IV型疾病(HR = 0.44; 90%CI,0.23-0.83; p = 0.015),7.0个月,17例反复性疾病(HR = 0.12; 90%CI,0.03-0.48; p = 0.004)。与控制臂相比,OS较高,中位数为29.6个月,与24.4个月(HR = 0.58; 90%CI,0.34-0.99; P = 0.046)。该益处是最值得注意的是III阶段至IV疾病的那些,在T形臂中未达到的生存中值与控制臂中的24.4个月(HR = 0.49; 90%CI,0.25-0.97; P = 0.041)。毒性在武器之间没有差异。结论:添加到具有先进/复发性HER2 / Neu-阳性USC的女性中的C / P增加PFS和OS,具有最大的益处,可用于治疗III阶段至IV疾病。

著录项

相似文献

  • 外文文献
  • 中文文献
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