← 返回

CAR-T 细胞在慢性淋巴细胞白血病中的应用

英文原题:CAR-T Cells in Chronic Lymphocytic Leukemia.

查看英文原题

CAR-T Cells in Chronic Lymphocytic Leukemia.

PubMed 2024/05/01(内容时间) Mediterr J Hematol Infect Dis Q3 · IF 2.3(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

随着基于布鲁顿激酶抑制剂(BTKi)、维奈克拉及抗 CD20 单克隆抗体的靶向疗法问世,慢性淋巴细胞白血病(CLL)患者的治疗结局已显著改善。然而,尽管疗效持续进步,对这些药物耐药的患者结局仍较差,需要更新且更有效的治疗策略。在这些新疗法中,一种潜在治愈方法是CAR-T(CAR-T)细胞疗法;该疗法在包括 B 细胞非霍奇金淋巴瘤(NHL)和 B 细胞急性淋巴细胞白血病(ALL)在内的多种 B 细胞恶性肿瘤中取得显著成功。然而,尽管 CAR-T 细胞最初也用于治疗 CLL,其在 CLL 患者中的疗效低于其他 B 细胞恶性肿瘤。本综述分析可能导致疗效不佳的机制,并重点介绍近期有望促使 CAR-T 细胞纳入复发/难治性 CLL 患者治疗方案的进展。

展开英文摘要原文

The treatment outcomes of patients with chronic lymphocytic leukemia (CLL) have considerably improved with the introduction of targeted therapies based on Bruton kinase inhibitors (BTKIs), venetoclax, and anti-CD20 monoclonal antibodies.

However, despite these consistent improvements, patients who become resistant to these agents have poor outcomes and need new and more efficacious therapeutic strategies. Among these new treatments, a potentially curative approach consists of the use of chimeric antigen receptor T (CAR-T) cell therapy, which achieved remarkable success in various B-cell malignancies, including B-cell Non-Hodgkin Lymphomas (NHLs) and B-acute lymphoblastic Leukemia (ALL).

However, although CAR-T cells were initially used for the treatment of CLL, their efficacy in CLL patients was lower than in other B-cell malignancies. This review analyses possible mechanisms of these failures, highlighting some recent developments that could offer the perspective of the incorporation of CAR-T cells in treatment protocols for relapsed/refractory CLL patients.

论文信息

作者
Testa U、Pelosi E、Castelli G、Fresa A、Laurenti L
第一作者单位
Istituto Superiore di Sanità, Roma, Italy.Italy
通讯作者单位
Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy. Sezione Di Ematologia. Roma, Italy.Italy
文献类型
综述
期刊
Mediterranean journal of hematology and infectious diseases2024
原文标识
PubMed 38882451 · DOI 10.4084/MJHID.2024.045