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整合以维奈克拉为基础的靶向和/或免疫治疗用于慢性淋巴细胞白血病

英文原题:Integrating venetoclax-based targeted and/or immune therapies for chronic lymphocytic leukemia.

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Integrating venetoclax-based targeted and/or immune therapies for chronic lymphocytic leukemia.

PubMed 2026/03/11(内容时间) Crit Rev Oncol Hematol Q1 · IF 6.2(JCR 2025)

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中文摘要

Venetoclax(VEN)是一种选择性 BCL-2 抑制剂,以 VEN 为基础的联合方案是现代慢性淋巴细胞白血病(CLL)管理的基石,可实现深度缓解和固定疗程、无化疗的治疗选择。本叙述性综述旨在概述 VEN 为基础的靶向治疗和免疫治疗联合方案在新诊断和复发/难治性 CLL 中的应用。

我们总结了评估 VEN 联合抗 CD20 单克隆抗体、Bruton 酪氨酸激酶抑制剂(BTKi)、双特异性抗体和嵌合抗原受体(CAR)T 细胞的关键临床试验。本文讨论的方案实现了高总缓解率、持久的无进展生存期和显著的可检测不到微小残留病率,通常转化为延长的无治疗间期。例如,固定疗程 VEN-奥妥珠单抗/利妥昔单抗方案优于化学免疫治疗,而 VEN 与 BTKi 的联合进一步改善了缓解深度并降低了耐药率。讨论了 MRD 指导策略,但其优于固定疗程方法尚未得到证实。还重点介绍了关于再治疗、序贯策略、剂量优化和下一代 BTKi 的新兴数据。

我们还指出了当前的知识空白,因为未来直接比较方案并整合 MRD 驱动决策的研究对于确定最佳治疗策略至关重要。

展开英文摘要原文

Venetoclax (VEN), a selective BCL-2 inhibitor and VEN-based combinations represent a cornerstone of modern chronic lymphocytic leukemia (CLL) management and allow deep remissions and fixed-duration, chemotherapy-free treatment options.

Our narrative review aims to provide an overview of VEN-based targeted and immunotherapy combinations in both newly-diagnosed and relapsed/refractory CLL.

We summarize pivotal clinical trials evaluating VEN in combination with anti-CD20 monoclonal antibodies, Bruton's tyrosine kinase inhibitors (BTKi), bispecific antibodies and chimeric antigen receptor (CAR) T-cells. The regimens we discuss in this paper achieved high overall response rates, durable progression-free survival, and substantial rates of undetectable minimal residual disease, often translating into prolonged treatment-free intervals.

For instance, fixed-duration VEN-obinutuzumab/rituximab regimens demonstrated superiority over chemoimmunotherapy, while combinations of VEN with BTKi further improved depth of response and reduced resistance rates. MRD-guided strategies are discussed, their superiority over fixed-duration approaches, however, remains unproven. Emerging data on retreatment, sequencing strategies, dose optimization, and next-generation BTKi are also highlighted.

We also identify current knowledge gaps because future studies directly comparing regimens and integrating MRD-driven decision-making will be critical to defining optimal therapeutic strategies.

论文信息

作者
Kegyes D、Muresan X、Bancos A、Mesaros O、Tigu AB、Borlea B、Gulei D、Bumbea H
第一作者单位
Department of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania; Department of Hematology, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.Italy
通讯作者单位
Department of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania; Department of Hematology, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania; Department of Hematology, Ion Chiricuta Oncology Institute, Cluj-Napoca, Romania. Electronic address: ciprian.tomuleasa@umfcluj.ro.Italy
文献类型
综述
期刊
Critical reviews in oncology/hematology2026 Jun
原文标识
PubMed 41825576 · DOI 10.1016/j.critrevonc.2026.105267