Gressett Sarah M, Shah Sachin R
Veterans Affairs North Texas Health Care System, Dallas, TX 75216, USA.
Ann Pharmacother. 2009 Mar;43(3):490-501. doi: 10.1345/aph.1L426. Epub 2009 Mar 3.
To review the serious and common toxicities of bevacizumab and describe their incidence, risk factors, presentation, pathophysiology, and management.
Literature for this review article was collected from PubMed, MEDLINE, and the proceedings of the American Society of Clinical Oncology (2000-November 2008). The key terms used in the search were: bevacizumab, vascular endothelial growth factor, angiogenesis inhibitors, toxicity, toxicity management, and adverse event.
Review articles, preclinical studies, and all published Phase 1-3 clinical trials were reviewed. The references listed in identified articles were examined for additional publications.
The biomedical literature from 2000 to 2008 confirms that bevacizumab carries serious and potentially life-threatening toxicity risks and emphasizes the importance of early recognition, continuous monitoring, and prompt management of these toxicities. Such toxicities include hemorrhage/bleeding, wound healing complications, gastrointestinal perforation, arterial thromboembolism, congestive heart failure, hypertension, proteinuria/nephrotic syndrome, infusion-related hypersensitivity reactions, and reversible posterior leukoencephalopathy syndrome. Patients at the highest risk for these toxicities are individuals with a history of hypertension, thromboembolism, bleeding, cardiovascular disease, or preexisting proteinuria, as these conditions may be exacerbated by bevacizumab use. Additionally, particular tumor types correlate with risk for individual toxicities; for example, patients with squamous non-small-cell lung cancer or rectal cancer have a higher risk of bleeding, those with renal cell carcinoma have a higher proteinuria risk, and patients with colorectal cancer have a higher risk of gastrointestinal perforation. Further investigation is warranted to develop effective management strategies for these toxicities.
As bevacizumab is becoming widely used in general oncology practice, it is important to understand the toxicities that can arise and to develop practice guidelines for their management.
回顾贝伐单抗的严重及常见毒性,并描述其发生率、危险因素、表现、病理生理学及处理方法。
本综述文章的文献收集自PubMed、MEDLINE以及美国临床肿瘤学会会议记录(2000年至2008年11月)。检索使用的关键词为:贝伐单抗、血管内皮生长因子、血管生成抑制剂、毒性、毒性处理及不良事件。
对综述文章、临床前研究以及所有已发表的1-3期临床试验进行了回顾。对已识别文章中列出的参考文献进行检查以获取更多出版物。
2000年至2008年的生物医学文献证实,贝伐单抗具有严重且可能危及生命的毒性风险,并强调早期识别、持续监测以及及时处理这些毒性的重要性。此类毒性包括出血、伤口愈合并发症、胃肠道穿孔、动脉血栓栓塞、充血性心力衰竭、高血压、蛋白尿/肾病综合征、输液相关的过敏反应以及可逆性后部白质脑病综合征。具有高血压、血栓栓塞、出血、心血管疾病或既往蛋白尿病史的个体发生这些毒性的风险最高,因为使用贝伐单抗可能会使这些情况恶化。此外,特定肿瘤类型与个体毒性风险相关;例如,鳞状非小细胞肺癌或直肠癌患者出血风险较高,肾细胞癌患者蛋白尿风险较高,而结直肠癌患者胃肠道穿孔风险较高。有必要进行进一步研究以制定针对这些毒性的有效处理策略。
由于贝伐单抗在肿瘤学常规实践中使用日益广泛,了解可能出现的毒性并制定管理实践指南非常重要。