CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Perspectives on T-cell engaging therapies in relapsed/refractory indolent non-Hodgkin lymphoma.
Perspectives on T-cell engaging therapies in relapsed/refractory indolent non-Hodgkin lymphoma.
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滤泡性淋巴瘤(FL)和边缘区淋巴瘤(MZL)是非霍奇金淋巴瘤(iNHL)的惰性亚型,以复发缓解的疾病进程为特征。T细胞衔接疗法作为一类有前景的新型治疗手段崭露头角,包括CD19靶向CAR-T 细胞疗法和CD3xCD20靶向双特异性抗体(BsABs)。本综述对其在复发/难治性(r/r)iNHL中的疗效和安全性以及后勤方面的考量进行了全面评估。
几项关键性 CAR-T 试验在 r/r FL 中显示出令人瞩目的缓解率和持久缓解,而 MZL 中的数据仍然稀缺。CAR-T 以单次输注给药,但需要复杂的后勤基础设施。不同的 BsAbs 已显示出良好的疗效,且急性毒性发生率较低。即用型可及性有利于其使用,尽管 BsAbs 的长期给药可能给患者带来沉重负担。长期感染风险是两种治疗都令人担忧的问题。目前仍缺乏直接比较 CAR-T 与 BsAbs 的临床研究。总结:CAR-T 和 BsAbs 均已证明作为 iNHL 治疗方式具有良好疗效。T 细胞衔接疗法的决策应针对患者个体因素和可及性进行定制。随访数据的成熟将进一步指导 FL 和 MZL 的循证治疗选择。
PURPOSE OF REVIEW: Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent subtypes of non-Hodgkin lymphoma (iNHL) characterized by a relapsing-remitting disease course. A promising novel therapeutic class emerges with T-cell engaging therapies, which include CD19 directed chimeric antigen receptor T-cell (CAR-T) therapy and CD3xCD20 directed bispecific antibodies (BsABs). This review provides a comprehensive evaluation of their efficacy and safety along with logistical considerations in relapsed/refractory (r/r) iNHL. RECENT FINDINGS: Several pivotal CAR-T trials have presented impressive response rates and durable remissions in r/r FL, while data in MZL is scarce.
CAR-T is given as a single infusion, but requires a complex logistical infrastructure. Different BsAbs have shown favorable efficacy with a lower rate of acute toxicities. Off-the-shelve availability favors its usability, although prolonged administration of BsAbs might impose a substantial burden for patients. Long-term infection risk is a concern for both treatments.
Clinical studies that directly compare CAR-T and BsAbs are still lacking. SUMMARY: Both CAR-T and BsAbs have demonstrated promising efficacy as treatment modalities in iNHL. Decision making for T-cell engaging therapies should be tailored to patient specific factors and availability. Maturation of follow-up data will further guide evidence-based treatment choices in FL and MZL.
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