决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Chimeric Antigen Receptor T-Cell Therapy for Hematologic Malignancies: A Practical Review.
CAR-T 细胞疗法已成为治疗血液系统恶性肿瘤的成熟治疗方法。
CAR-T 细胞疗法已成为治疗血液系统恶性肿瘤的既定治疗方法。该领域持续快速发展,新一代构建体正在设计中,以增强增殖能力,并实现长期持久性和更高疗效,同时总体毒性发生率更低。CAR-T疗法的初始临床应用主要集中在复发和/或难治性血液系统恶性肿瘤,美国食品药品监督管理局批准的靶向CD19的CAR-T产品可用于B细胞急性淋巴细胞白血病和低级别及高级别B细胞非霍奇金淋巴瘤,靶向B细胞成熟抗原的产品可用于多发性骨髓瘤。细胞因子释放综合征和免疫效应细胞相关神经毒性综合征已被认为是与这些新型疗法相关的类别特异性毒性。在本综述中,我们重点关注CAR-T疗法在成人血液系统恶性肿瘤患者中的临床应用,包括可及性问题、门诊给药以及将患者转诊至CAR-T治疗中心的适当时机。
Chimeric antigen receptor T-cell (CAR-T) therapy has become an established therapeutic approach for the treatment of hematologic malignancies. The field continues to evolve rapidly and newer-generation constructs are being designed to enhance proliferative capacity, and achieve long-term persistence and greater efficacy with an overall lower incidence of toxicity. Initial clinical application of CAR-T therapies has focused on relapsed and/or refractory hematologic malignancies, and Food and Drug Administration-approved CAR-T products targeting CD19 are available for B-cell acute lymphoblastic leukemia and low- and high-grade B-cell non-Hodgkin lymphoma, and targeting B-cell maturation antigen are available for multiple myeloma. Cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome have been recognized as class specific toxicities associated with these novel therapies. In this review, we focus on the clinical application of CAR-T therapies in adult patients with hematologic malignancies, including access issues, outpatient administration, and appropriate timing for referring a patient to a CAR-T treatment center.
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