Hepatotoxicity of tyrosine kinase inhibitors: clinical and regulatory perspectives
- PMID: 23620168
- DOI: 10.1007/s40264-013-0048-4
Hepatotoxicity of tyrosine kinase inhibitors: clinical and regulatory perspectives
Abstract
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.
Similar articles
-
Hepatotoxicity of Small Molecule Protein Kinase Inhibitors for Cancer.Cancers (Basel). 2023 Mar 14;15(6):1766. doi: 10.3390/cancers15061766. Cancers (Basel). 2023. PMID: 36980652 Free PMC article. Review.
-
[Hepatotoxicity of tyrosine kinase inhibitors: Mechanisms involved and practical implications].Bull Cancer. 2018 Mar;105(3):290-298. doi: 10.1016/j.bulcan.2017.11.015. Epub 2018 Feb 19. Bull Cancer. 2018. PMID: 29471963 Review. French.
-
Cardiovascular safety of tyrosine kinase inhibitors: with a special focus on cardiac repolarisation (QT interval).Drug Saf. 2013 May;36(5):295-316. doi: 10.1007/s40264-013-0047-5. Drug Saf. 2013. PMID: 23620167 Review.
-
Formation of reactive metabolites and management of tyrosine kinase inhibitor-induced hepatotoxicity: a literature review.Expert Opin Drug Metab Toxicol. 2015 Feb;11(2):231-42. doi: 10.1517/17425255.2015.983075. Epub 2014 Nov 15. Expert Opin Drug Metab Toxicol. 2015. PMID: 25400226 Review.
-
Mechanisms of toxicity associated with six tyrosine kinase inhibitors in human hepatocyte cell lines.J Appl Toxicol. 2018 Mar;38(3):418-431. doi: 10.1002/jat.3551. Epub 2017 Oct 26. J Appl Toxicol. 2018. PMID: 29072336
Cited by
-
Combined sunitinib and radiation therapy for preoperative treatment of soft tissue sarcoma: results of a phase I trial of the German interdisciplinary sarcoma group (GISG-03).Radiat Oncol. 2016 Jun 3;11:77. doi: 10.1186/s13014-016-0654-2. Radiat Oncol. 2016. PMID: 27255678 Free PMC article. Clinical Trial.
-
Pharmacokinetics and disposition of anlotinib, an oral tyrosine kinase inhibitor, in experimental animal species.Acta Pharmacol Sin. 2018 Jun;39(6):1048-1063. doi: 10.1038/aps.2017.199. Epub 2018 Apr 5. Acta Pharmacol Sin. 2018. PMID: 29620050 Free PMC article.
-
A phase Ib/II translational study of sunitinib with neoadjuvant radiotherapy in soft-tissue sarcoma.Br J Cancer. 2014 Dec 9;111(12):2254-61. doi: 10.1038/bjc.2014.537. Epub 2014 Oct 16. Br J Cancer. 2014. PMID: 25321190 Free PMC article. Clinical Trial.
-
Multicenter phase II study of sequential radioembolization-sorafenib therapy for inoperable hepatocellular carcinoma.PLoS One. 2014 Mar 10;9(3):e90909. doi: 10.1371/journal.pone.0090909. eCollection 2014. PLoS One. 2014. PMID: 24614178 Free PMC article. Clinical Trial.
-
Rare but Serious: Ibrutinib Induced Liver Failure.Hemasphere. 2019 Oct 22;3(6):e307. doi: 10.1097/HS9.0000000000000307. eCollection 2019 Dec. Hemasphere. 2019. PMID: 31976481 Free PMC article. No abstract available.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials