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新型药物时代加速期慢性淋巴细胞白血病与 Richter 转化

英文原题:Accelerated Chronic Lymphocytic Leukemia and Richter Transformation in the Era of Novel Agents.

查看英文原题

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

PubMed 2023/09/04(内容时间) Acta Haematol Q2 · IF 2.8(JCR 2025)

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研究概要

CLL 领域近年来取得了重大进展,但 A-CLL 和 RT 仍是「未满足的需求」相关议题,需要进一步研究以确定最佳诊断方法和更有效的治疗。

中文摘要

背景:近年来慢性淋巴细胞白血病(CLL)领域取得巨大进展,治疗方式发生变革,目前以靶向治疗为基础,疗效良好、预后优化。尽管如此,CLL 仍可能呈现或进展为“加速期 CLL”(A-CLL)或“Richter 转化”(RT);这两类疾病进程更具侵袭性,诊断和治疗仍面临挑战。本综述总结了 A-CLL 的诊断方法,以及 A-CLL 和 RT 现有治疗与临床试验的最新知识;这两类疾病仍存在未满足需求,需要进一步基础和临床研究。摘要:A-CLL 是一种罕见且诊断不足的疾病,可能处于 CLL 与 RT 之间的“灰色地带”,总体预后居中。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 Ki-67 指数较高。由于疾病罕见,治疗方法尚未确立,但新型药物似乎有效,尤其是 Bruton 酪氨酸激酶抑制剂(BTKi)。RT 的标准治疗仍为化学免疫治疗,适合且有应答的患者随后接受干细胞移植,但总体预后差。近期开始采用新的治疗方式,包括以新型药物(BTKi、venetoclax)抑制 B 细胞,以及 T 细胞衔接疗法(免疫检查点抑制剂、双特异性抗体 [BiTE] 或嵌合抗原受体 [CAR] 技术)、抗体药物偶联物或药物联合治疗。CAR-T 和 BiTE 似乎均有前景,尤其是与 BTKi 联合时,但现有证据仍不足,通常应将患者纳入临床试验。要点:CLL 领域近年来取得重大进展,但 A-CLL 和 RT 仍属于未满足的医疗需求,需要进一步研究以确定最佳诊断方法和更有效的治疗。

展开英文摘要原文

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.

论文信息

作者
Levy Yurkovski I、Tadmor T
单位
Hematology Unit, Bnai-Zion Medical Center, Haifa, Israel.Israel
文献类型
综述
期刊
Acta haematologica2024
原文标识
PubMed 37666234 · DOI 10.1159/000533664