贝伐单抗诱导结直肠癌患者肠穿孔

Sun-Young Baek, Seung Hun Lee, Seung-Hyun Lee
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引用次数: 4

摘要

贝伐单抗是一种靶向血管内皮生长因子的重组人源化单克隆抗体,是一种被批准用于治疗多发性实体瘤的抗血管生成药物。它已显示出作为一种治疗转移性结直肠癌的临床药物的前景,特别是与化疗联合使用[1]。随着贝伐单抗使用的增加,高血压、蛋白尿、出血、血栓形成、瘘管形成和肠穿孔等严重不良反应的报道也越来越频繁[24]。在贝伐单抗治疗结直肠癌的两项3期试验中,肠穿孔是一种罕见的不良事件,尽管严重且致命,但发生率仅为1.5%和1.1%。在这里,本研究的目的是确定贝伐单抗在结直肠癌中引起的肠道穿孔的临床特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bevacizumab induced intestinal perforation in patients with colorectal cancer
Bevacizumab, a recombinant humanized monoclonal antibody targeting vascular endothelial growth factor, is an antiangiogenic agent approved for the treatment of multiple solid tumors. It has shown promise as a clinical agent against metastatic colorectal cancer, and particularly in combination with chemotherapy [1]. With increased use of bevacizumab, serious adverse effects are being reported more frequently, including hypertension, proteinuria, hemorrhage, thrombosis, fistula formation, and bowel perforation [24]. In two phase 3 trials of bevacizumab in colorectal cancer, intestinal perforation was an uncommon adverse event occurring at rates of only 1.5% and 1.1%, though serious and lethal. Here, the purpose of this study is to identify the clinical characteristics of intestinal perforation induced by bevacizumab in colorectal cancers.
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