特刊:CAR-T细胞治疗血液恶性肿瘤

Immunomedicine Pub Date : 2022-08-24 DOI:10.1002/imed.1038
Yongxian Hu MD, PhD, He Huang MD, PhD
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引用次数: 0

摘要

嵌合抗原受体T (CAR-T)细胞疗法已经彻底改变了复发/难治性(R/R) b细胞来源的血液系统恶性肿瘤的治疗,包括急性淋巴细胞白血病(ALL)、b细胞非霍奇金淋巴瘤(B-NHL)和多发性骨髓瘤(MM)。cd19靶向CAR-T细胞在R/R ALL中的完全缓解率约为90%,在R/R NHL中的完全缓解率约为50%,而bcma靶向CAR-T细胞在R/R MM中的完全缓解率约为50% - 80%。值得注意的是,美国食品和药物管理局已经批准了6种CAR-T细胞产品(tisagenlecleucel, axicabtagene ciloleucel, brexabtagene自甲醇,isocabtagene maraleucel, idecabtagene vicleucel和ciltacabtagene自甲醇)用于治疗R/R B-NHL, R/R ALL和R/R MM。CAR-T细胞输注后,一些患者可能对这种治疗无反应或快速复发,这可能是由于CAR-T细胞功能障碍和持久性差或特异性抗原的调节。因此,必须研究替代治疗策略。此外,越来越多的研究发现了具有治疗效果和效用的新抗原靶点,用于生成CAR-T细胞治疗急性髓性白血病(AML)。CAR-T细胞治疗期间的安全性是另一个重要问题,涉及诸如细胞因子释放综合征、免疫效应细胞相关神经毒性综合征(ICANS)、全血细胞减少症和感染等并发症。尽管这些副作用大多数都很小,但危及生命的危险仍然存在。对严重不良事件的谨慎治疗需要多学科合作,不仅需要肿瘤学家的参与,也需要其他内科医生的参与,以保证及时诊断和治疗。因此,了解CAR-T细胞治疗的新进展至关重要。这一期《免疫医学》特刊聚焦于CAR-T细胞治疗血液恶性肿瘤的新进展。王向民(https://doi.org/10.1002/imed.1030)的综述总结了非bcma靶向CAR-T细胞治疗MM的方法,包括CS1、CD38、CD138、NKG2D、CD70、TACI等新靶点可能具有预防复发和提高治疗效率的潜力。Elaine Tan Su Yin (https://doi.org/10.1002/imed.1039)综述了目前cd20靶向CAR-T细胞治疗血液系统恶性肿瘤,特别是R/R B-NHL的突破和未来前景。Huang Yue (https://doi.org/10.1002/imed.1031)综述了目前CAR-T细胞治疗在AML临床前研究和临床试验中的成就和潜在的AML相关细胞标志物,并讨论了CAR-T细胞治疗在AML患者中的未来发展方向。郝媛媛(https://doi.org/10.1002/imed.1029)综述了肿瘤源性外泌体(TEXs)对T细胞亚群存活和功能的影响及其临床应用。本期特刊还包含三篇报道CAR-T细胞治疗临床试验的原创研究文章。周凌辉等(https://doi.org/10.1002/imed.1036)报道了CAR-T细胞治疗后感染的数据,发现这是CD19 CAR-T细胞治疗的血液系统恶性肿瘤患者常见的并发症,这意味着临床医生应该更加重视这种情况。唐凯婷等(https://doi.org/10.1002/imed.1037)报道了3例富有同情心的CAR-T细胞治疗晚期B-ALL的病例,并分享了他们治疗高疾病负担患者的经验。Yue Huang等(https://doi.org/10.1002/imed.1032)报道了一名高白血病负担和中枢神经系统受累的R/R ALL患者,对供体来源的hla匹配异体CAR-T治疗有反应,并取得了快速的cr。我们感谢所有作者的深刻贡献。这期特刊概述了CAR-T细胞治疗的最新进展,包括CAR-T细胞的功能、不同的应用以及应对策略的并发症。我们希望这个问题能够吸引研究人员,因为他们正在探索CAR-T细胞治疗的基础和临床方面。
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Special issue: CAR-T cell therapy for hematological malignancies

Chimeric antigen receptor T (CAR-T) cell therapy has revolutionized the treatment of relapsed/refractory (R/R) B-cell derived hematological malignancies, including acute lymphoblastic leukemia (ALL), B-cell non-Hodgkin lymphoma (B-NHL), and multiple myeloma (MM). CD19-targeted CAR-T cells yield complete remission (CR) rates of about 90% in R/R ALL and about 50% in R/R NHL, respectively, while BCMA-targeted CAR-T cells yield CR rate of about 50%−80% in R/R MM. Notably, the US Food and Drug Administration have approved six CAR-T cell products (tisagenlecleucel, axicabtagene ciloleucel, brexucabtagene autoleucel, lisocabtagene maraleucel, idecabtagene vicleucel, and ciltacabtagene autoleucel) for the treatment of R/R B-NHL, R/R ALL, and R/R MM. However, some patients might not respond to such therapy or quickly relapse after CAR-T cell infusion, which is likely due to the dysfunction and poor persistence of CAR-T cells or the modulation of specific antigen. Thus, alternative treatment strategies must be investigated. In addition, accumulating research have been conducted to discover novel target of antigens with therapeutic efficacy and utility for generating CAR-T cells against acute myeloid leukemia (AML). Safety during CAR-T cell treatment is another important issue, concerning complications such as cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome (ICANS), pancytopenia, and infection. Despite the fact that the majority of those adverse effects are minimal, the risk of a life-threatening situation still exists. Cautious treatment for severe adverse events requires a multidisciplinary approach with involvement of not only oncologists but also other internal medicine doctors to guarantee diagnosis and treatment in time. Therefore, it is of vital importance to understand the novel advances of CAR-T cell therapy.

This special issue of ImmunoMedicine focuses on novel developments of CAR-T cell therapy for hematological malignancies. The review from Xiangmin Wang (https://doi.org/10.1002/imed.1030) summarized the non-BCMA targeted CAR-T cell therapies for MM. Novel targets including CS1, CD38, CD138, NKG2D, CD70, TACI, and etc. might have the potential to prevent the recurrence and enhance treatment efficiency. The review from Elaine Tan Su Yin (https://doi.org/10.1002/imed.1039) summarized the current breakthrough and future perspectives of CD20-targeted CAR-T cell therapy for hematologic malignancies, especially for R/R B-NHL. The review from Yue Huang (https://doi.org/10.1002/imed.1031) summarized the current achievement and potential AML-associated cell markers of CAR-T cell therapy in AML preclinical studies and clinical trials, and discusses the future directions of CAR-T cell therapy in patients with AML. The review from Yuanyuan Hao (https://doi.org/10.1002/imed.1029) summarized the effects of tumor-derived exosomes (TEXs) on the survival and functions of T cell subsets, as well as their clinical applications.

This special issue also contains three original research articles reporting clinical trials of CAR-T cell therapy. Linghui Zhou et al. (https://doi.org/10.1002/imed.1036) reported the data of infections post CAR-T cell therapy, and found that it was a common complication in patients with hematological malignancies treated by CD19 CAR-T cells, which means clinicians should pay more attention to such situations. Kaiting Tang et al. (https://doi.org/10.1002/imed.1037) presented three cases of compassionate CAR-T cell therapy in advanced B-ALL, and shared their experiences on treating patients with high disease burden. Yue Huang et al. (https://doi.org/10.1002/imed.1032) reported an R/R ALL patient with high leukemia burden and central nervous system involvement, who responded to donor-derived HLA-matched allogeneic CAR-T treatment and achieved quick CR.

We thank all the authors for their insightful contributions. This special issue provides an overview of the current knowledge regarding the most recent advances of CAR-T cell therapy, including CAR-T cell function, diverse applications, and complications with coping strategies. We hope that this issue will appeal to researchers as they explore fundamental and clinical aspects of CAR-T cell therapy.

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