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淋巴瘤中基于嵌合抗原受体T细胞的疗法:当前实践与展望综述

CAR T-Based Therapies in Lymphoma: A Review of Current Practice and Perspectives.

作者信息

Sheikh Semira, Migliorini Denis, Lang Noémie

机构信息

Department of Hematology, Universitätsspital Basel, 4031 Basel, Switzerland.

Department of Oncology, Hôpitaux Universitaires de Genève, 1205 Geneva, Switzerland.

出版信息

Biomedicines. 2022 Aug 12;10(8):1960. doi: 10.3390/biomedicines10081960.

DOI:10.3390/biomedicines10081960
PMID:36009506
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9405554/
Abstract

While more than half of non-Hodgkin lymphomas (NHL) can be cured with modern frontline chemoimmunotherapy regimens, outcomes of relapsed and/or refractory (r/r) disease in subsequent lines remain poor, particularly if considered ineligible for hematopoietic stem cell transplantation. Hence, r/r NHLs represent a population with a high unmet medical need. This therapeutic gap has been partially filled by adoptive immunotherapy. CD19-directed autologous chimeric antigen receptor (auto-CAR) T cells have been transformative in the treatment of patients with r/r B cell malignancies. Remarkable response rates and prolonged remissions have been achieved in this setting, leading to regulatory approval from the U.S. Food and Drug Administration (FDA) of four CAR T cell products between 2017 and 2021. This unprecedented success has created considerable enthusiasm worldwide, and autologous CAR T cells are now being moved into earlier lines of therapy in large B cell lymphoma. Herein, we summarize the current practice and the latest progress of CD19 auto-CAR T cell therapy and the management of specific toxicities and discuss the place of allogeneic CAR T development in this setting.

摘要

虽然超过一半的非霍奇金淋巴瘤(NHL)可以通过现代一线化疗免疫治疗方案治愈,但后续治疗线中复发和/或难治性(r/r)疾病的预后仍然很差,特别是如果被认为不符合造血干细胞移植条件。因此,r/r NHL患者群体存在高度未满足的医疗需求。过继性免疫疗法部分填补了这一治疗空白。针对CD19的自体嵌合抗原受体(auto-CAR)T细胞在r/r B细胞恶性肿瘤患者的治疗中具有变革性。在这种情况下已取得了显著的缓解率和延长的缓解期,导致2017年至2021年间美国食品药品监督管理局(FDA)批准了四种CAR T细胞产品。这一前所未有的成功在全球范围内引发了极大的热情,自体CAR T细胞目前正被应用于大B细胞淋巴瘤的更早期治疗。在此,我们总结了CD19自体CAR T细胞治疗的当前实践和最新进展以及特定毒性的管理,并讨论了同种异体CAR T细胞在这种情况下的发展地位。