Tang Chloe Pek Sang, McMullen Julie, Tam Constantine
a Department of Haematology , St Vincent's Hospital Melbourne , Fitzroy , Australia.
b Baker IDI Heart and Diabetes Institute , Melbourne , Australia.
Leuk Lymphoma. 2018 Jul;59(7):1554-1564. doi: 10.1080/10428194.2017.1375110. Epub 2017 Sep 13.
The development of bruton tyrosine kinase inhibitors (BTKi) has been a significant advancement in the treatment of chronic lymphocytic leukemia and related B-cell malignancies. As experience in using ibrutinib increased, the first drug to be licensed in its class, atrial fibrillation (AF) emerged as an important side effect. The intersection between BTKi therapy for B-cell malignancies and AF represents a complex area of management with scant evidence for guidance. Consideration needs to be taken regarding the interplay of increased bleeding risk versus thromboembolic complications of AF, drug interactions between ibrutinib and anticoagulants and antiarrhythmic agents, and the potential for other, as yet seldom reported cardiac side effects. This review describes the current knowledge regarding BTKi and potential pathophysiologic mechanisms of AF and discusses the management of BTKi-associated AF. Finally, a review of the second generation BTKi is provided and gaps in knowledge in this evolving field are highlighted.
布鲁顿酪氨酸激酶抑制剂(BTKi)的研发是慢性淋巴细胞白血病及相关B细胞恶性肿瘤治疗领域的一项重大进展。随着第一代获许可使用的该类药物伊布替尼使用经验的增加,心房颤动(AF)成为一种重要的副作用。BTKi治疗B细胞恶性肿瘤与AF之间的交叉领域是一个复杂的管理领域,几乎没有证据可供指导。需要考虑AF出血风险增加与血栓栓塞并发症之间的相互作用、伊布替尼与抗凝剂和抗心律失常药物之间的药物相互作用,以及其他尚未被充分报道的心脏副作用的可能性。本综述描述了关于BTKi和AF潜在病理生理机制的现有知识,并讨论了BTKi相关AF的管理。最后,对第二代BTKi进行了综述,并强调了这一不断发展领域中的知识空白。