Side effects of anti-cancer molecular-targeted therapies (not monoclonal antibodies)

被引:28
作者
de Castro, Gilberto, Jr.
Awada, Ahmad
机构
[1] Inst Jules Bordet, Med Oncol Clin, B-1000 Brussels, Belgium
[2] Univ Sao Paulo, Sch Med, Hosp Clin, Radiol Dept InRad,Clin Oncol Serv, Sao Paulo, Brazil
关键词
anti-angiogenic agents; bortezomib; farnesyltransferase inhibitors; lenalidomide; molecular-targeted therapies; tyrosine-kinase inhibitors;
D O I
10.1097/01.cco.0000228733.55132.ea
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review Major advances have been achieved in the field of biologically based therapies for cancer in the last few years, and some of the recently approved 'molecular-targeted therapies' are now being used in daily clinical practice. We aim to review some aspects of the toxicity and safety of small-molecule anti-cancer molecular-targeted therapies; with some insights into the physiopathology and predictive factors of toxicity, its correlation with response, and how to E prevent and overcome it: Recent findings As a whole, small-molecule molecular-targeted therapies are well tolerated: Their toxic profile is favorable, but during the drug development process some severe (sometimes lethal) toxicities have been observed, such as interstitial lung disease in patients treated with drugs targeting the I epidermal growth factor receptor. Pharmacogenomic studies can help us to identify those patients with well characterized polymorphisms; and to define the best-tolerated-and most effective treatments. Summary Molecular-targeted therapies have a good toxicity profile in general; however, some patients are exquisitely sensitive to developing particular and severe toxicities related to these drugs.
引用
收藏
页码:307 / 315
页数:9
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