Sheikh Semira, Migliorini Denis, Lang Noémie
Department of Hematology, Universitätsspital Basel, 4031 Basel, Switzerland.
Department of Oncology, Hôpitaux Universitaires de Genève, 1205 Geneva, Switzerland.
Biomedicines. 2022 Aug 12;10(8):1960. doi: 10.3390/biomedicines10081960.
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.
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。