TY - JOUR
T1 - Drug-drug interactions with tyrosine-kinase inhibitors
T2 - A clinical perspective
AU - van Leeuwen, Roelof W. F.
AU - van Gelder, Teun
AU - Mathijssen, Ron H. J.
AU - Jansman, Frank G. A.
N1 - Copyright © 2014 Elsevier Ltd. All rights reserved.
PY - 2014/7
Y1 - 2014/7
N2 - 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.
AB - 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.
KW - CHRONIC MYELOID-LEUKEMIA
KW - ADVANCED SOLID TUMORS
KW - IMATINIB MESYLATE GLEEVEC
KW - PROTON PUMP INHIBITOR
KW - ST-JOHNS-WORT
KW - HEALTHY-SUBJECTS
KW - PHASE-I
KW - CYP3A4 INHIBITION
KW - GRAPEFRUIT JUICE
KW - PROTEIN-BINDING
U2 - 10.1016/S1470-2045(13)70579-5
DO - 10.1016/S1470-2045(13)70579-5
M3 - Review article
C2 - 24988935
SN - 1470-2045
VL - 15
SP - E315-E326
JO - Lancet Oncology
JF - Lancet Oncology
IS - 8
ER -