...
首页> 外文期刊>Medicine. >Chemotherapy plus bevacizumab versus chemotherapy plus cetuximab as first-line treatment for patients with metastatic colorectal cancer: Results of a registry-based cohort analysis
【24h】

Chemotherapy plus bevacizumab versus chemotherapy plus cetuximab as first-line treatment for patients with metastatic colorectal cancer: Results of a registry-based cohort analysis

机译:转移性结直肠癌患者的化学疗法加贝伐珠单抗与化学疗法加西妥昔单抗作为一线治疗:基于登记的队列分析结果

获取原文
   

获取外文期刊封面封底 >>

       

摘要

The present observational cohort study was designed to elucidate the efficacy and safety profile of bevacizumab or cetuximab with chemotherapy as the first-line treatment in Chinese patients with metastatic colorectal cancer (mCRC). Clinical data were collected from a single-center registry study where mCRC patients received first-line fluoropyrimidine-based chemotherapy combined with either bevacizumab (188 patients with KRAS wild-type or mutated tumors) or cetuximab (101 patients with KRAS wild-type tumors) between January 2009 and December 2013. The Kaplan–Meier method was used for survival analysis. Cox proportional hazards model was used for estimating the prognostic and predictive values of clinicopathological characteristics. No statistically significant difference was observed between the bevacizumab and cetuximab groups in terms of median progression-free survival (PFS) (10.6 vs 8.7 months, P = 0.317), median overall survival (OS) (27.7 vs 28.3 months, P = 0.525), or overall response rate (43.1% vs 53.5%, P = 0.108). For the subset of patients with peritoneal dissemination, bevacizumab-based triplet appears to be superior to cetuximab-based triplet as measured by PFS (9.6 vs 6.1 months) and OS (26.3 vs 12.7 months), but not for patients without peritoneal dissemination (PFS, 10.6 vs 9.1 months; OS, 27.9 vs 30.7 months) (all unadjusted and adjusted interaction P < 0.05). Our study suggests that bevacizumab- or cetuximab-based regimens have similar effectiveness as first-line treatment of mCRC in Chinese population. Patients with peritoneal dissemination were likely to gain more benefit from bevacizumab than cetuximab treatment. Future prospective studies are required to further confirm these results.
机译:本观察性队列研究旨在阐明贝伐单抗或西妥昔单抗联合化疗作为中国转移性结直肠癌(mCRC)患者的一线治疗的疗效和安全性。临床数据来自单中心注册表研究,其中mCRC患者接受基于一线氟嘧啶的一线化疗联合贝伐单抗(188例KRAS野生型或突变肿瘤患者)或西妥昔单抗(101例KRAS野生型肿瘤患者)。在2009年1月至2013年12月之间。采用Kaplan-Meier方法进行生存分析。 Cox比例风险模型用于估计临床病理特征的预后和预测值。贝伐单抗和西妥昔单抗组之间在无进展生存期中位数(PFS)(10.6 vs 8.7个月,P = 0.317),中位总生存期(OS)(27.7 vs 28.3个月,P = 0.525)之间没有统计学上的显着差异。 ,或整体回应率(43.1%vs 53.5%,P = 0.108)。对于具有腹膜扩散的患者亚群,通过PFS(9.6 vs 6.1个月)和OS(26.3 vs 12.7个月)测量,基于贝伐单抗的三联体似乎优于基于西妥昔单抗的三联体,但对于没有腹膜扩散的患者(PFS)则不然,分别为10.6和9.1个月;操作系统,分别为27.9和30.7个月)(所有未经调整和调整的交互作用P <0.05)。我们的研究表明,基于贝伐单抗或西妥昔单抗的治疗方案与中国人群mCRC一线治疗的疗效相似。与西妥昔单抗治疗相比,腹膜播散患者可能从贝伐单抗中获益更多。需要进一步的前瞻性研究以进一步证实这些结果。

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