Hepatotoxicity of Tyrosine Kinase Inhibitors: Clinical and Regulatory Perspectives

被引:0
|
作者
Rashmi R. Shah
Joel Morganroth
Devron R. Shah
机构
[1] Rashmi Shah Consultancy Ltd,
[2] eResearch Technology,undefined
来源
Drug Safety | 2013年 / 36卷
关键词
Imatinib; Sorafenib; Sunitinib; Gefitinib; Erlotinib;
D O I
暂无
中图分类号
学科分类号
摘要
The introduction of small-molecule tyrosine kinase inhibitors (TKIs) in clinical oncology has transformed the treatment of certain forms of cancers. As of 31 March 2013, 18 such agents have been approved by the US Food and Drug Administration (FDA), 15 of these also by the European Medicines Agency (EMA), and a large number of others are in development or under regulatory review. Unexpectedly, however, their use has been found to be associated with serious toxic effects on a number of vital organs including the liver. Drug-induced hepatotoxicity has resulted in withdrawal from the market of many widely used drugs and is a major public health issue that continues to concern all the stakeholders. This review focuses on hepatotoxic potential of TKIs. The majority of TKIs approved to date are reported to induce hepatic injury. Five of these (lapatinib, pazopanib, ponatinib, regorafenib and sunitinib) are sufficiently potent in this respect as to require a boxed label warning. Onset of TKI-induced hepatotoxicity is usually within the first 2 months of initiating treatment, but may be delayed, and is usually reversible. Fatality from TKI-induced hepatotoxicity is uncommon compared to hepatotoxic drugs in other classes but may lead to long-term consequences such as cirrhosis. Patients should be carefully monitored for TKI-induced hepatotoxicity, the management of which requires individually tailored reappraisal of the risk/benefit. The risk is usually manageable by dose adjustment or a switch to a suitable alternative TKI. Confirmation of TKI-induced hepatotoxicity can present challenges in the presence of hepatic metastasis and potential drug interactions. Its diagnosis in a patient with TKI-sensitive cancer requires great care if therapy with the TKI suspected to be causal is to be modified or interrupted as a result. Post-marketing experience with drugs such as imatinib, lapatinib and sorafenib suggests that the hepatotoxic safety of all the TKIs requires diligent surveillance.
引用
收藏
页码:491 / 503
页数:12
相关论文
共 50 条
  • [1] Hepatotoxicity of Tyrosine Kinase Inhibitors: Clinical and Regulatory Perspectives
    Shah, Rashmi R.
    Morganroth, Joel
    Shah, Devron R.
    DRUG SAFETY, 2013, 36 (07) : 491 - 503
  • [2] Hepatotoxicity of tyrosine kinase inhibitors: Mechanisms involved and practical implications
    Bechade, Dominique
    Chakiba, Camille
    Desjardin, Marie
    Becouarn, Yves
    Fonck, Marianne
    BULLETIN DU CANCER, 2018, 105 (03) : 290 - 298
  • [3] Clinical pharmacology of tyrosine kinase inhibitors becoming generic drugs: the regulatory perspective
    Eckstein, Niels
    Roeper, Lea
    Haas, Bodo
    Potthast, Henrike
    Hermes, Ulrike
    Unkrig, Christoph
    Naumann-Winter, Frauke
    Enzmann, Harald
    JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2014, 33
  • [4] Hepatotoxicity of epidermal growth factor receptor - tyrosine kinase inhibitors (EGFR-TKIs)
    Zhu, Lulin
    Yang, Xinxin
    Wu, Shanshan
    Dong, Rong
    Yan, Youyou
    Lin, Nengming
    Zhang, Bo
    Tan, Biqin
    DRUG METABOLISM REVIEWS, 2024, 56 (03) : 302 - 317
  • [5] Cardiotoxicity induced by tyrosine kinase inhibitors
    Orphanos, George S.
    Ioannidis, George N.
    Ardavanis, Alexandros G.
    ACTA ONCOLOGICA, 2009, 48 (07) : 964 - 970
  • [6] Role of tyrosine kinase inhibitors in the treatment of advanced colorectal cancer
    Gravalos, Cristina
    Cassinello, Javier
    Fernandez-Ranada, Isabel
    Holgado, Esther
    CLINICAL COLORECTAL CANCER, 2007, 6 (10) : 691 - 699
  • [7] Clinical development of EGFR-tyrosine kinase inhibitors in Japan
    Nakagawa, Kazuhiko
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2006, 58 (Suppl 1) : S33 - S37
  • [8] Clinical development of EGFR-tyrosine kinase inhibitors in Japan
    Kazuhiko Nakagawa
    Cancer Chemotherapy and Pharmacology, 2006, 58 : 33 - 37
  • [9] Tyrosine kinase inhibitors: a clinical perspective.
    Goel S.
    Mani S.
    Perez-Soler R.
    Current Oncology Reports, 2002, 4 (1) : 9 - 19
  • [10] Thyroid dysfunctions induced by tyrosine kinase inhibitors
    Fallahi, Poupak
    Ferrari, Silvia M.
    Vita, Roberto
    Di Domenicantonio, Andrea
    Corrado, Alda
    Benvenga, Salvatore
    Antonelli, Alessandro
    EXPERT OPINION ON DRUG SAFETY, 2014, 13 (06) : 723 - 733