Chung Clement
Houston Methodist West Hospital, Houston, TX, USA.
Am J Health Syst Pharm. 2025 Mar 11. doi: 10.1093/ajhp/zxaf058.
In an effort to expedite the publication of articles, AJHP is posting manuscripts online as soon as possible after acceptance. Accepted manuscripts have been peer-reviewed and copyedited, but are posted online before technical formatting and author proofing. These manuscripts are not the final version of record and will be replaced with the final article (formatted per AJHP style and proofed by the authors) at a later time.
This article concisely evaluates current targeted therapies that have received regulatory approval for chronic lymphocytic leukemia (CLL). Mechanisms of molecular pathogenesis and their therapeutic implications, current and novel targeted therapies, and supportive care are discussed.
CLL is a common lymphoproliferative neoplasm of mature but immunologically incompetent B cells in older adults. Over the past 2 decades, robust research has shown that CLL pathogenesis is a multistep process that includes, but is not limited to, (1) clonal selection, expansion, and transformation; (2) an aberrant B cell signaling pathways; (3) sequence heterogeneity in the gene encoding the immunoglobulin heavy chain variable region (IGHV); (4) impaired apoptosis; and (5) interactions between CLL cells and their microenvironment. The development of oral targeted therapies against some of these molecular abnormalities has led to improved survival outcomes over traditional chemoimmunotherapy. Current oral targeted therapies that have received regulatory approval include continuous therapy with Bruton's tyrosine kinase inhibitors (BTKis) and fixed-duration therapy with the B cell leukemia/lymphoma-2 inhibitor (BCL-2i) venetoclax. These agents may be used either alone or in combination in the treatment-naive setting, as well as in relapsed or refractory disease. This review contributes to understanding of the molecular pathogenesis of CLL with therapeutic implications. It summarizes key advances in oral targeted therapies and emerging innovative targeted therapies (eg, novel BTKis, BTK degraders, and novel BCL-2is) and highlights supportive care in optimizing treatment-related adverse effects.
Treatment options for CLL continue to evolve. Current treatment selection is based on clinical and patient-specific considerations. Emerging novel therapies to overcome treatment resistance and strategies to optimize supportive care generate opportunities for pharmacists to advance practice and improve patient safety.
为加快文章发表速度,美国卫生系统药剂师协会(AJHP)在稿件被接受后尽快将其在线发布。已接受的稿件已经过同行评审和编辑,但在进行技术排版和作者校样之前就已在线发布。这些稿件并非最终记录版本,稍后将被最终文章(按照AJHP风格排版并经作者校样)取代。
本文简要评估了目前已获得监管批准用于慢性淋巴细胞白血病(CLL)的靶向治疗方法。讨论了分子发病机制及其治疗意义、当前和新型靶向治疗方法以及支持性治疗。
CLL是一种常见于老年人的成熟但免疫功能不全B细胞的淋巴增殖性肿瘤。在过去20年中,大量研究表明CLL发病机制是一个多步骤过程,包括但不限于:(1)克隆选择、扩增和转化;(2)异常的B细胞信号通路;(3)编码免疫球蛋白重链可变区(IGHV)的基因中的序列异质性;(4)凋亡受损;(5)CLL细胞与其微环境之间的相互作用。针对其中一些分子异常的口服靶向治疗的发展已使生存结果优于传统的化学免疫疗法。目前已获得监管批准的口服靶向治疗方法包括使用布鲁顿酪氨酸激酶抑制剂(BTKis)进行持续治疗以及使用B细胞白血病/淋巴瘤-2抑制剂(BCL-2i)维奈克拉进行固定疗程治疗。这些药物可单独使用或联合用于初治患者,以及复发或难治性疾病患者。本综述有助于理解CLL的分子发病机制及其治疗意义。它总结了口服靶向治疗的关键进展以及新兴的创新靶向治疗方法(如新型BTKis、BTK降解剂和新型BCL-2is),并强调了在优化治疗相关不良反应方面的支持性治疗。
CLL的治疗选择不断发展。目前的治疗选择基于临床和患者个体因素。新兴的克服治疗耐药性的新型疗法以及优化支持性治疗的策略为药剂师提升业务水平和提高患者安全性创造了机会。