Kuss Bryone, Nagarajan Chandramouli, Hsieh Wen Son, Cheah Chan Yoon
Molecular Medicine and Genetics, Flinders University, Adelaide, SA, Australia.
Haematology Department, Flinders Medical Centre and SA Pathology, Adelaide, SA, Australia.
Leuk Lymphoma. 2022 Dec;63(12):2785-2794. doi: 10.1080/10428194.2022.2098289. Epub 2022 Jul 19.
Treatment of chronic lymphocytic leukemia (CLL) has been transformed in the past two decades. The introduction of targeted therapies has improved patient outcomes and the deliverability of effective therapies. Making the best use of the next wave of Bruton's tyrosine kinase (BTK) inhibitors requires an understanding of the nuances that separate the drugs in this class of agents. This paper reviews the newer BTK inhibitors and provides practical guidance on the management of CLL using acalabrutinib. Acalabrutinib is a safe and efficacious BTKi in the treatment of CLL. While some side effects appear to be an "on-target" effect of BTK inhibition, the selectivity of second-generation covalent BTK inhibitors such as acalabrutinib may result in a favorable safety profile due to less off-target kinase inhibition. Acalabrutinib represents a well-tolerated and effective alternative to ibrutinib in the management of CLL.
在过去二十年中,慢性淋巴细胞白血病(CLL)的治疗发生了变革。靶向治疗的引入改善了患者的治疗效果以及有效治疗的可及性。要充分利用下一波布鲁顿酪氨酸激酶(BTK)抑制剂,需要了解这类药物中各药物之间的细微差别。本文回顾了新型BTK抑制剂,并提供了使用阿卡替尼治疗CLL的实用指南。阿卡替尼是一种治疗CLL安全有效的BTK抑制剂。虽然一些副作用似乎是BTK抑制的“靶向”效应,但第二代共价BTK抑制剂(如阿卡替尼)的选择性可能因其较少的脱靶激酶抑制作用而带来良好的安全性。在CLL的治疗中,阿卡替尼是一种耐受性良好且有效的伊布替尼替代药物。