Department of Medical Oncology, Institute of Oncology Ljubljana, Slovenia.
Anticancer Res. 2011 May;31(5):1777-82.
The antivascular endothelial growth factor monoclonal antibody bevacizumab with infusional 5-fluorouracil, leucovorin and irinotecan (FOLFIRI) is a standard first-line treatment option for metastatic colorectal cancer. However, clinical data for capecitabine and irinotecan (XELIRI) with bevacizumab are limited.
A retrospective study was conducted on 139 patients with metastatic colorectal cancer to assess the efficacy and safety of first-line bevacizumab in combination with XELIRI or FOLFIRI. Primary endpoints were overall response rate (ORR), disease control rate and radical resection rate. Secondary endpoints included overall survival (OS), progression-free survival (PFS) and safety.
No significant differences in efficacy were observed between patients administered XELIRI or FOLFIRI with bevacizumab. The ORR, median OS and PFS and recorded adverse events (AEs) were comparable to those previously reported, with no new or unexpected AEs observed.
Bevacizumab is similarly efficacious and well tolerated when administered with XELIRI or FOLFIRI.
贝伐珠单抗是一种抗血管内皮生长因子的单克隆抗体,与氟尿嘧啶、亚叶酸钙和伊立替康(FOLFIRI)联合使用,是转移性结直肠癌的标准一线治疗选择。然而,贝伐珠单抗联合卡培他滨和伊立替康(XELIRI)的临床数据有限。
对 139 例转移性结直肠癌患者进行了回顾性研究,以评估一线贝伐珠单抗联合 XELIRI 或 FOLFIRI 的疗效和安全性。主要终点是总缓解率(ORR)、疾病控制率和根治性切除率。次要终点包括总生存期(OS)、无进展生存期(PFS)和安全性。
接受 XELIRI 或 FOLFIRI 联合贝伐珠单抗治疗的患者在疗效方面无显著差异。ORR、中位 OS 和 PFS 以及记录的不良事件(AE)与先前报道的相似,未观察到新的或意外的 AE。
贝伐珠单抗联合 XELIRI 或 FOLFIRI 的疗效相似,且耐受性良好。