Literature DB >> 28627951

The safety of Bruton's tyrosine kinase inhibitors for the treatment of chronic lymphocytic leukemia.

Phu N Tran1, Susan O'Brien1.   

Abstract

INTRODUCTION: The approval of ibrutinib has revolutionized the therapeutic landscape of chronic lymphocytic leukemia (CLL). Currently ibrutinib is indicated for patients that are both treatment naïve as well as those with relapsed CLL. Ibrutinib is generally well-tolerated with durable responses that improve over time in most patients. Important toxicities include atrial fibrillation and bleeding. Areas cover: This review covers the pharmacokinetics, pharmacodynamics, safety and efficacy of ibrutinib in the treatment of CLL. We also compare ibrutinib with other kinase inhibitors and chemoimmunotherapy regimens using data from clinical trials. A literature search utilized the PubMed database. Expert opinion: Despite the efficacy and tolerability of ibrutinib, important questions remain, which include selection of patients receiving ibrutinib in the first and subsequent lines of treatment, optimal dosing, sequential use of ibrutinib versus other kinase inhibitors and combination therapy. Prospective studies should incorporate minimal residual disease (MRD) status as a clinical endpoint to determine whether patients can be taken off kinase inhibitors.

Entities:  

Keywords:  BTK inhibitors; chemoimmunotherapy; chronic lymphocytic leukemia; ibrutinib; safety; toxicity

Mesh:

Substances:

Year:  2017        PMID: 28627951     DOI: 10.1080/14740338.2017.1344213

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  2 in total

1.  Ibrutinib Therapy and Mycobacterium chelonae Skin and Soft Tissue Infection.

Authors:  Khalid M Dousa; Ahmed Babiker; Daniel Van Aartsen; Neel Shah; Robert A Bonomo; John L Johnson; Marion J Skalweit
Journal:  Open Forum Infect Dis       Date:  2018-07-18       Impact factor: 3.835

2.  Safety, pharmacokinetics and pharmacodynamics of BI 705564, a highly selective, covalent inhibitor of Bruton's tyrosine kinase, in Phase I clinical trials in healthy volunteers.

Authors:  Tobias Litzenburger; Jürgen Steffgen; Ewald Benediktus; Fabian Müller; Armin Schultz; Elliott Klein; Meera Ramanujam; Christian Harcken; Alpana Gupta; Jing Wu; Sabrina Wiebe; Xiujiang Li; Mary Flack; Steven J Padula; Sudha Visvanathan; Andreas Hünnemeyer; Jianan Hui
Journal:  Br J Clin Pharmacol       Date:  2020-11-20       Impact factor: 3.716

  2 in total

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