City of Hope, Lennar Foundation Cancer Center, Irvine, CA.
City of Hope, Lennar Foundation Cancer Center, Irvine, CA.
Semin Hematol. 2024 Apr;61(2):119-130. doi: 10.1053/j.seminhematol.2024.01.001. Epub 2024 Jan 5.
Immunotherapies, such as chimeric antigen receptor (CAR) T-cell therapy and bispecific antibodies or T-cell engagers, have revolutionized the treatment landscape for various B-cell malignancies, including B-acute lymphoblastic leukemia and many non-Hodgkin lymphomas. Despite their significant impact on these malignancies, their application in chronic lymphocytic leukemia (CLL) management is still largely under investigation. Although the initial success of CD19-directed CAR T-cell therapy was observed in 3 multiply relapsed CLL patients, with 2 of them surviving over 10 years without relapse, recent CAR T-cell therapy trials in CLL have shown reduced response rates compared to their efficacy in other B-cell malignancies. One of the challenges with using immunotherapy in CLL is the compromised T-cell fitness from persistent CLL-related antigenic stimulation, and an immunosuppressive tumor microenvironment (TME). These challenges underscore a critical gap in therapeutic options for CLL patients intolerant or resistant to current therapies, emphasizing the imperative role of effective immunotherapy. Encouragingly, innovative strategies are emerging to overcome these challenges. These include integrating synergistic agents like ibrutinib to enhance CAR T-cell function and persistence and engineering newer CAR T-cell constructs targeting diverse antigens or employing dual-targeting approaches. Bispecific antibodies are an exciting "off-the-shelf" prospect for these patients, with their investigation in CLL currently entering the realm of clinical trials. Additionally, the development of allogeneic CAR T-cells and natural killer (NK) cells from healthy donors presents a promising solution to address the diminished T-cell fitness observed in CLL patients. This comprehensive review delves into the latest insights regarding the role of immunotherapy in CLL, the complex landscape of resistance mechanisms, and a spectrum of innovative approaches to surmount therapeutic challenges.
免疫疗法,如嵌合抗原受体(CAR)T 细胞疗法和双特异性抗体或 T 细胞衔接器,已经彻底改变了各种 B 细胞恶性肿瘤的治疗格局,包括 B 急性淋巴细胞白血病和许多非霍奇金淋巴瘤。尽管它们对这些恶性肿瘤有重大影响,但它们在慢性淋巴细胞白血病(CLL)管理中的应用仍在很大程度上有待研究。尽管 CD19 靶向 CAR T 细胞疗法在 3 例多次复发的 CLL 患者中取得了初步成功,其中 2 例患者在没有复发的情况下存活了 10 年以上,但最近 CLL 的 CAR T 细胞治疗试验显示,与其他 B 细胞恶性肿瘤相比,其反应率降低。在 CLL 中使用免疫疗法的挑战之一是持续的 CLL 相关抗原刺激导致 T 细胞功能受损,以及免疫抑制的肿瘤微环境(TME)。这些挑战凸显了对于不能耐受或对现有疗法耐药的 CLL 患者的治疗选择存在重大差距,强调了有效免疫疗法的重要作用。令人鼓舞的是,正在出现创新策略来克服这些挑战。这些策略包括整合协同剂,如伊布替尼,以增强 CAR T 细胞的功能和持久性,并设计针对多种抗原的新型 CAR T 细胞结构或采用双靶向方法。双特异性抗体是这些患者令人兴奋的“现成”选择,目前正在对其进行 CLL 的临床试验研究。此外,从健康供体中开发同种异体 CAR T 细胞和自然杀伤(NK)细胞为解决 CLL 患者中观察到的 T 细胞功能下降提供了一个有前途的解决方案。本综述深入探讨了免疫疗法在 CLL 中的作用、耐药机制的复杂景观以及克服治疗挑战的一系列创新方法的最新见解。