Therapeutic advances in chronic lymphocytic leukemia: A focus on molecular pathogenesis, targeted therapies, and supportive care.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Clement Chung
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引用次数: 0

Abstract

Purpose: 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.

Summary: 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) 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.

Conclusion: 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.

慢性淋巴细胞白血病的治疗进展:关注分子发病机制、靶向治疗和支持治疗。
免责声明:为了加快文章的发表,AJHP在接受稿件后将尽快在网上发布。被接受的稿件已经过同行评审和编辑,但在技术格式化和作者校对之前会在网上发布。这些手稿不是记录的最终版本,稍后将被最终文章(按照AJHP风格格式化并由作者校对)所取代。目的:本文简要评价目前已获得监管机构批准的慢性淋巴细胞白血病(CLL)靶向治疗。分子发病机制及其治疗意义,目前和新的靶向治疗和支持治疗进行了讨论。摘要:CLL是老年人成熟但免疫功能不全的B细胞的一种常见淋巴增生性肿瘤。在过去的20年里,大量的研究表明CLL的发病是一个多步骤的过程,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)免疫球蛋白重链可变区(IGHV)编码基因序列异质性;(4)细胞凋亡受损;(5) CLL细胞与其微环境的相互作用。针对这些分子异常的口服靶向治疗的发展已经导致了比传统化学免疫治疗更好的生存结果。目前已获得监管部门批准的口服靶向治疗包括布鲁顿酪氨酸激酶抑制剂(BTKis)的持续治疗和B细胞白血病/淋巴瘤-2抑制剂(BCL-2i) venetoclax的固定持续治疗。这些药物可单独或联合使用,在治疗初期,以及复发或难治性疾病。本文综述有助于了解CLL的分子发病机制和治疗意义。它总结了口服靶向治疗和新兴创新靶向治疗(如新型BTKis、BTK降解剂和新型BCL-2is)的关键进展,并强调了优化治疗相关不良反应的支持治疗。结论:CLL的治疗方案在不断发展。目前的治疗选择是基于临床和患者的具体考虑。新兴的新疗法,以克服治疗阻力和策略,优化支持性护理产生机会药师推进实践和提高患者的安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.90
自引率
18.50%
发文量
341
审稿时长
3-8 weeks
期刊介绍: The American Journal of Health-System Pharmacy (AJHP) is the official publication of the American Society of Health-System Pharmacists (ASHP). It publishes peer-reviewed scientific papers on contemporary drug therapy and pharmacy practice innovations in hospitals and health systems. With a circulation of more than 43,000, AJHP is the most widely recognized and respected clinical pharmacy journal in the world.
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