Nagle Sarah J, Garfall Alfred L, Stadtmauer Edward A
From the Division of Hematology/Oncology, Department of Medicine and Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Cancer J. 2016 Jan-Feb;22(1):27-33. doi: 10.1097/PPO.0000000000000166.
Relapsed and refractory hematologic malignancies have a very poor prognosis. Chimeric antigen receptor T cells are emerging as a powerful therapy in this setting. Early clinical trials of genetically modified T cells for the treatment of non-Hodgkin lymphoma, chronic lymphocytic leukemia, and acute lymphoblastic leukemia have shown high complete response rates in patients with few therapeutic options. Exploration is ongoing for other hematologic malignancies including multiple myeloma, acute myeloid leukemia, and Hodgkin lymphoma (HL). At the same time, the design and production of chimeric antigen receptor T cells are being advanced so that this therapy can be more widely utilized. Cytokine release syndrome and neurotoxicity are common, but they are treatable and fully reversible. This review will review available data as well as future developments and challenges in the field.
复发难治性血液系统恶性肿瘤的预后非常差。嵌合抗原受体T细胞正在成为这种情况下的一种有效治疗方法。针对非霍奇金淋巴瘤、慢性淋巴细胞白血病和急性淋巴细胞白血病的基因改造T细胞早期临床试验表明,在治疗选择有限的患者中,完全缓解率很高。目前正在探索将其用于包括多发性骨髓瘤、急性髓系白血病和霍奇金淋巴瘤(HL)在内的其他血液系统恶性肿瘤。与此同时,嵌合抗原受体T细胞的设计和生产也在不断改进,以便这种疗法能够得到更广泛的应用。细胞因子释放综合征和神经毒性很常见,但它们是可治疗且完全可逆的。本综述将回顾该领域的现有数据以及未来的发展和挑战。