Journal article
Ibrutinib, but not zanubrutinib, induces platelet receptor shedding of GPIb-IX-V complex and integrin αIIbβ3 in mice and humans
G Dobie, FA Kuriri, MMA Omar, F Alanazi, AM Gazwani, CPS Tang, DMY Sze, SM Handunnetti, C Tam, DE Jackson
Blood Advances | ELSEVIER | Published : 2019
Abstract
The Bruton's tyrosine kinase (Btk) inhibitor ibrutinib has proven to be efficacious in the treatment of B-cell chronic lymphocytic leukemia (B-CLL) and related diseases. However, a major adverse side effect of ibrutinib is bleeding, including major hemorrhages. The bleeding associated with ibrutinib use is thought to be due to a combination of on-target irreversible Btk inhibition, as well as off-target inhibition of other kinases, including EGFR, ITK, JAK3, and Tec kinase. In this study, we investigated the effects of ibrutinib vs zanubrutinib (a more selective Btk inhibitor) on platelet activation, glycoprotein expression, and thrombus formation. Ibrutinib, but not zanubrutinib, induced a ..
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Funding Acknowledgements
This work was supported by a sponsored research agreement from Beigene, Pty Ltd (D.E.J.); funding from CLL Global Research Foundation (C.T.); and a postgraduate scholarship from Jazan University and the Ministry of Higher Education (Riyadh, Saudi Arabia) (G.D.).