Bevacizumab toxicities and their management in ovarian cancer

被引:100
作者
Randall, Leslie M. [1 ]
Monk, Bradley J. [1 ]
机构
[1] Univ Calif Irvine, Med Ctr, Div Gynecol Oncol, Dept Obstet & Gynecol,Chao Family Comprehens Canc, Orange, CA 92868 USA
关键词
Bevacizumab; Ovarian cancer; Toxicity; METASTATIC COLORECTAL-CANCER; PLATINUM-RESISTANT OVARIAN; PHASE-III TRIAL; PRIMARY PERITONEAL; RECURRENT OVARIAN; 1ST-LINE THERAPY; ANTI-ANGIOGENESIS; PLUS IRINOTECAN; FALLOPIAN-TUBE; VEGF;
D O I
10.1016/j.ygyno.2010.02.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives. The purpose of this review is to discuss the side effect profile of bevacizumab, to discuss proposed mechanisms of these toxicities, and to provide suggestions for management of adverse events. Methods. A search of MEDLINE and ASCO and SGO abstract databases of articles published between January 1970 and August 2009 addressing the toxicity of bevacizumab in solid tumors was conducted. Reporting was limited to best available evidence including any available phase III studies and ovarian cancer phase II studies. Original publications addressing underlying mechanisms of bevacizumab toxicities were included. Results. Extensive experience with bevacizumab has proven the agent to be generally well tolerated, with an adverse event profile distinct from traditional cytotoxic chemotherapy and likely peculiar to its novel mechanism of action. The most common bevacizumab-attributable adverse event, hypertension, can be medically-managed, but more serious adverse events such as bowel perforation require drug discontinuation. Conclusions. Current best evidence supports the use of bevacizumab in selected patients, and safe administration of bevacizumab requires an understanding of the management of adverse events attributable to its use. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:497 / 504
页数:8
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