Accelerated Chronic Lymphocytic Leukemia and Richter Transformation in the Era of Novel Agents.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Accounts of Chemical Research Pub Date : 2024-01-01 Epub Date: 2023-09-04 DOI:10.1159/000533664
Ilana Levy Yurkovski, Tamar Tadmor
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引用次数: 0

Abstract

Background: Tremendous developments in the field of chronic lymphocytic leukemia (CLL) in recent years have led to a revolutionary change in the treatment approach, which today is based on targeted treatments with a good response and optimal prognosis. Nevertheless, CLL can present or progress to "accelerated CLL" (A-CLL) or to "Richter transformation" (RT) and these two entities have a more aggressive course and are still characterized by challenges in the fields of diagnosis and therapy. In the current review, we summarized the latest knowledge in terms of diagnostic approaches to A-CLL, available treatments and clinical trials, for both A-CLL and RT which still pose an unmet need and require additional basic and clinical investigations.

Summary: A-CLL is a rare and underdiagnosed entity that probably stands in the "gray zone" between CLL and RT, generally holding an intermediate prognosis. Its diagnosis is mainly based on histological findings including expanded proliferation centers, increased mitotic activity, and/or high Ki-67 index. Due to its rarity, its treatment approach has still not been defined, but it seems that novel agents, especially Bruton tyrosine kinase inhibitors (BTKi), are effective. As for RT, the standard therapy still consists of chemo-immunotherapy followed by stem-cell transplantation for fit responders with a dismal prognosis. New approaches are recently adopted including B-cell inhibition via novel agents (BTKi, venetoclax), T-cell engagers (checkpoint inhibitors, bispecific antibodies [BiTe] or the chimeric antigen receptor [CAR] technology), antibody-drug conjugates, or drug combinations. Although both CAR-T and BiTe seem promising, especially when combined with BTKi, evidence is still insufficient, and patients should generally be recruited in clinical trials.

Key messages: The field of CLL has been a subject of major advances in recent years, but A-CLL and RT remain topics of "unmet need" and require further studies to identify the best diagnostic approach and a more effective treatment.

新型药物时代的慢性淋巴细胞白血病加速和里氏转化。
背景:近年来,慢性淋巴细胞白血病(CLL)领域取得了巨大的发展,导致治疗方法发生了革命性的变化,如今的治疗方法以靶向治疗为基础,具有良好的反应和最佳的预后。尽管如此,CLL 仍有可能发展为 "加速型 CLL"(A-CLL)或 "里克特转化"(RT),这两种实体的病程更具侵袭性,在诊断和治疗领域仍面临挑战。在本综述中,我们总结了 A-CLL 诊断方法、现有治疗方法和临床试验方面的最新知识,A-CLL 和 RT 仍有未满足的需求,需要进行更多的基础和临床研究。摘要:A-CLL 是一种罕见且诊断不足的疾病,可能处于 CLL 和 RT 之间的 "灰色地带",预后一般处于中等水平。其诊断主要基于组织学发现,包括增殖中心扩大、有丝分裂活动增加和/或高 Ki-67 指数。由于其罕见性,其治疗方法仍未确定,但新型药物,尤其是布鲁顿酪氨酸激酶抑制剂(BTKi)似乎很有效。至于 RT,标准疗法仍包括化疗免疫疗法,然后对预后不良的合适应答者进行干细胞移植。最近采用的新方法包括通过新型药物(BTKi、venetoclax)抑制B细胞、T细胞吞噬(检查点抑制剂、双特异性抗体[BiTe]或嵌合抗原受体[CAR]技术)、抗体药物共轭物或药物组合。虽然CAR-T和BiTe似乎都很有前景,尤其是与BTKi联合使用时,但目前证据仍不充分,临床试验一般应招募患者:CLL领域近年来取得了重大进展,但A-CLL和RT仍是 "未满足需求 "的主题,需要进一步研究以确定最佳诊断方法和更有效的治疗方法。
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
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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