Hepatotoxicity of targeted therapy for cancer

被引:26
作者
Lee, Kirsty Wai-Chung [1 ,2 ]
Chan, Stephen Lam [1 ,2 ,3 ]
机构
[1] Chinese Univ Hong Kong, Hong Kong Canc Inst, State Key Lab Oncol South China, Sir YK Pao Ctr Canc,Dept Clin Oncol, Shatin, Hong Kong, Peoples R China
[2] Prince Wales Hosp, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Inst Digest Dis, Shatin, Hong Kong, Peoples R China
关键词
CYP polymorphisms; hepatitis reactivation; hepatotoxicity; immunotherapy; molecular targeted therapy; monoclonal antibodies; multikinase inhibitors; pharmacogenomics; tyrosine kinase inhibitors; CELL LUNG-CANCER; TYROSINE KINASE INHIBITOR; INDUCED LIVER-INJURY; HEPATITIS-B REACTIVATION; PHASE-II TRIAL; IMATINIB MESYLATE; VIRUS REACTIVATION; TREATED PATIENTS; DRUG-METABOLISM; GEFITINIB;
D O I
10.1080/17425255.2016.1190831
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Introduction: Understanding the mechanism of DILI with MTA, and how to avoid and manage these toxicities is essential for minimising inferior cancer treatment outcomes. An organised and comprehensive overview of MTA-associated hepatotoxicity is lacking; this review aims to fill the gap. Areas covered: A literature review was performed based on published case reports and relevant studies or articles pertaining to the topics on PubMed. Food and Drug Administration drug information documents and search on the US National Library of Medicine LiverTox database was performed for all relevant MTA. Expert opinion: MTA-associated hepatotoxicity is common but rarely fatal. The pattern of hepatotoxicity is predominantly idiosyncratic. Pharmacogenomics show potential in predicting patients at risk of poorly metabolising or developing immunoallergic responses to MTA, but prospective data is scant. Preventing reactivation of viral hepatitis using anti-viral drugs, and avoidance of drug combinations at high risk of negative interactions are the most readily preventable measures for DILI.
引用
收藏
页码:789 / 802
页数:14
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