Literature DB >> 32940733

Drug interactions with Bruton's tyrosine kinase inhibitors: clinical implications and management.

Karen M Fancher1,2, Jeremy J Pappacena3.   

Abstract

Bruton's tyrosine kinase (BTK) plays an essential role in B-cell development, differentiation and B-cell receptor (BCR) signaling. The use of Bruton's tyrosine kinase inhibitors (BTKi) in the treatment of lymphoid malignancies has dramatically increased, owing to both impressive efficacy and ease of administration. However, BTKi have a range of drug-drug and drug-food interactions, which may alter drug efficacy and/or increase toxicity. Healthcare professionals should be aware of the probability of drug interactions with BTKi and make recommendations accordingly. In this article, we discuss the relevant drug-drug and drug-food interactions associated with ibrutinib, acalabrutinib, and zanubrutinib, and provide clinical practice recommendations for managing these interactions based on the available literature.

Entities:  

Keywords:  Acalabrutinib; Bruton’s tyrosine kinase inhibitor; Drug–Drug interactions; Drug–Food interactions; Ibrutinib; Zanubrutinib

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Year:  2020        PMID: 32940733     DOI: 10.1007/s00280-020-04137-6

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  2 in total

1.  Intentional Modulation of Ibrutinib Pharmacokinetics through CYP3A Inhibition.

Authors:  Eric D Eisenmann; Qiang Fu; Elizabeth M Muhowski; Yan Jin; Muhammad Erfan Uddin; Dominique A Garrison; Robert H Weber; Jennifer Woyach; John C Byrd; Alex Sparreboom; Sharyn D Baker
Journal:  Cancer Res Commun       Date:  2021-11-09

2.  PROTAC-Mediated Degradation of Bruton's Tyrosine Kinase as a Therapeutic Strategy for Cancer.

Authors:  Robert B Kargbo
Journal:  ACS Med Chem Lett       Date:  2021-04-12       Impact factor: 4.345

  2 in total

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