Drug-drug interactions with tyrosine-kinase inhibitors: a clinical perspective
- PMID: 24988935
- DOI: 10.1016/S1470-2045(13)70579-5
Drug-drug interactions with tyrosine-kinase inhibitors: a clinical perspective
Abstract
In the past decade, many tyrosine-kinase inhibitors have been introduced in oncology and haemato-oncology. Because this new class of drugs is extensively used, serious drug-drug interactions are an increasing risk. In this Review, we give a comprehensive overview of known or suspected drug-drug interactions between tyrosine-kinase inhibitors and other drugs. We discuss all haemato-oncological and oncological tyrosine-kinase inhibitors that had been approved by Aug 1, 2013, by the US Food and Drug Administration or the European Medicines Agency. Various clinically relevant drug interactions with tyrosine-kinase inhibitors have been identified. Most interactions concern altered bioavailability due to altered stomach pH, metabolism by cytochrome P450 isoenzymes, and prolongation of the QTc interval. To guarantee the safe use of tyrosine-kinase inhibitors, a drugs review for each patient is needed. This Review provides specific recommendations to guide haemato-oncologists, oncologists, and clinical pharmacists, through the process of managing drug-drug interactions during treatment with tyrosine-kinase inhibitors in daily clinical practice.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Comment in
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Drug-drug interactions with tyrosine-kinase inhibitors.Lancet Oncol. 2014 Sep;15(10):e416. doi: 10.1016/S1470-2045(14)70187-1. Lancet Oncol. 2014. PMID: 25186045 No abstract available.
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Drug interactions between tyrosine-kinase inhibitors and acid suppressive agents: more than meets the eye.Lancet Oncol. 2014 Oct;15(11):e469-70. doi: 10.1016/S1470-2045(14)70458-9. Lancet Oncol. 2014. PMID: 25281461 No abstract available.
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Drug interactions between tyrosine-kinase inhibitors and acid suppressive agents: more than meets the eye-Authors' reply.Lancet Oncol. 2014 Oct;15(11):e470-1. doi: 10.1016/S1470-2045(14)70459-0. Lancet Oncol. 2014. PMID: 25281462 No abstract available.
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