Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Nat Rev Clin Oncol. 2019 Jun;16(6):372-385. doi: 10.1038/s41571-019-0184-6.
The successes with chimeric antigen receptor (CAR) T cell therapy in early clinical trials involving patients with pre-B cell acute lymphoblastic leukaemia (ALL) or B cell lymphomas have revolutionized anticancer therapy, providing a potentially curative option for patients who are refractory to standard treatments. These trials resulted in rapid FDA approvals of anti-CD19 CAR T cell products for both ALL and certain types of B cell lymphoma - the first approved gene therapies in the USA. However, growing experience with these agents has revealed that remissions will be brief in a substantial number of patients owing to poor CAR T cell persistence and/or cancer cell resistance resulting from antigen loss or modulation. Furthermore, the initial experience with CAR T cells has highlighted challenges associated with manufacturing a patient-specific therapy. Understanding the limitations of CAR T cell therapy will be critical to realizing the full potential of this novel treatment approach. Herein, we discuss the factors that can preclude durable remissions following CAR T cell therapy, with a primary focus on the resistance mechanisms that underlie disease relapse. We also provide an overview of potential strategies to overcome these obstacles in an effort to more effectively incorporate this unique therapeutic strategy into standard treatment paradigms.
嵌合抗原受体 (CAR) T 细胞疗法在涉及前体 B 细胞急性淋巴细胞白血病 (ALL) 或 B 细胞淋巴瘤患者的早期临床试验中的成功,彻底改变了癌症治疗方法,为那些对标准治疗方法产生耐药性的患者提供了一种潜在的治愈选择。这些试验导致抗 CD19 CAR T 细胞产品在美国迅速获得 FDA 批准,用于 ALL 和某些类型的 B 细胞淋巴瘤 - 这是美国批准的首批基因治疗药物。然而,随着这些药物的应用经验不断增加,由于 CAR T 细胞持续存在不良和/或由于抗原丢失或调节导致的癌细胞耐药性,大量患者的缓解将是短暂的。此外,CAR T 细胞的初步应用经验突出了与制造患者特异性治疗相关的挑战。了解 CAR T 细胞治疗的局限性对于充分发挥这种新型治疗方法的潜力至关重要。本文讨论了 CAR T 细胞治疗后可能无法持久缓解的因素,主要侧重于导致疾病复发的耐药机制。我们还概述了克服这些障碍的潜在策略,以努力更有效地将这种独特的治疗策略纳入标准治疗模式。