The first Bruton's tyrosine kinase (BTK) inhibitor ibrutinib was approved by the US Food and Drug Administration (FDA) in 2014 for treatment of chronic lymphocytic leukemia (CLL). First-generation BTK inhibitors have revolutionized the treatment of lymphoproliferative disorders but carry risk of dermatologic toxicities such as ecchymoses, rash, and skin infection.1
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Vilasi et al. (2024) studied this question.
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