Nair Ranjit, Neelapu Sattva S
Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX, 77030, USA.
Best Pract Res Clin Haematol. 2018 Sep;31(3):293-298. doi: 10.1016/j.beha.2018.07.011. Epub 2018 Aug 1.
Relapsed or refractory aggressive B-cell lymphoma has an extremely poor prognosis and efforts to develop novel therapies for these patients have failed for almost four decades until the advent of chimeric antigen receptor (CAR) T-cell therapy. Within the last one year, two anti-CD19 CAR T-cell therapy products, axicabtagene ciloleucel and tisagenlecleucel, were approved by the United States Food and Drug Administration for the treatment of relapsed or refractory large B-cell lymphoma after at least two lines of systemic therapy based on multicenter single-arm phase two clinical trials. Here, we will discuss the different components of the CAR construct and their mechanisms of action, the role of conditioning chemotherapy, the efficacy and toxicity observed with anti-CD19 CAR T-cell therapies in aggressive B-cell lymphomas, and emerging strategies to further improve the safety and efficacy of these highly promising approaches.
复发或难治性侵袭性B细胞淋巴瘤预后极差,在嵌合抗原受体(CAR)T细胞疗法出现之前,近四十年来为这些患者开发新疗法的努力均以失败告终。在过去一年中,基于多中心单臂二期临床试验,两种抗CD19 CAR T细胞疗法产品——阿基仑赛注射液和替雷利珠单抗,被美国食品药品监督管理局批准用于治疗经至少两线全身治疗后的复发或难治性大B细胞淋巴瘤。在此,我们将讨论CAR构建体的不同组成部分及其作用机制、预处理化疗的作用、抗CD19 CAR T细胞疗法在侵袭性B细胞淋巴瘤中的疗效和毒性,以及进一步提高这些极具前景的疗法的安全性和疗效的新兴策略。