CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Case Report: Subtotal Lymphoid and Total Marrow Irradiation as Bridge Therapy to CD19-Directed CAR T Cells in a Chemorefractory DLBCL With Leukemic Involvement.
Case Report: Subtotal Lymphoid and Total Marrow Irradiation as Bridge Therapy to CD19-Directed CAR T Cells in a Chemorefractory DLBCL With Leukemic Involvement.
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CAR-T 细胞疗法已经改变了复发/难治性弥漫大B细胞淋巴瘤(R/R DLBCL)的挽救治疗策略。在产品制造期间,CAR-T 细胞输注前维持疾病控制(即所谓的桥接治疗)是优化结局的重要步骤。在可能的桥接治疗中,放射治疗(RT)是一种有价值的选择,尤其是当疾病局限时。
在此,我们首次报告一例化疗难治性转化型DLBCL患者,表现为淋巴结、结外和大量骨髓(BM)淋巴瘤浸润并伴有白血病样受累,通过次全淋巴/全骨髓照射联合噻替派,随后回输CD34+自体造血干细胞,成功桥接至CD19靶向CAR-T 细胞治疗。这种新型桥接方案使淋巴结和BM肿瘤体积显著缩小,同时在CAR-T 细胞输注前改善了血细胞计数。治疗后1、3和6个月进行的PET-CT扫描和BM评估显示疾病完全缓解。约1年时因CD19抗原逃逸在淋巴结发生复发,而BM仍无疾病。这种扩展放疗方法可能是一种有效的桥接治疗,适用于适合CAR-T 细胞治疗且呈现高肿瘤负荷的化疗难治性DLBCL患者,包括伴有白血病样受累的大量BM浸润。这一初步证据值得在更多患者中加以证实。
CAR T cell therapy has transformed the salvage approach for relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). Maintaining disease control before CAR T cell infusion during product manufacturing (so-called bridging therapy) is an important step to optimizing outcome. Among possible bridging therapies, radiation therapy (RT) represents a valuable option, particularly when the disease is limited.
Here, we report for the first time on a patient with chemorefractory-transformed DLBCL showing nodal, extranodal, and massive bone marrow (BM) lymphoma infiltration associated with leukemic involvement, a successful bridge therapy to CD19-directed CAR T cell therapy by subtotal lymphoid/total marrow irradiation plus thiothepa followed by reinfusion of CD34+ autologous hematopoietic stem cells. Such a novel bridging regimen allowed a significant reduction of nodal and BM tumor volume while improving blood cell count before CAR T cell infusion.
The PET-CT scan and BM evaluation performed at 1, 3, and 6 months after treatment showed complete remission of the disease. A relapse occurred at almost 1 year in lymph nodes because of CD19 antigen escape while the BM remained free of disease. This extended radiotherapy approach may be an effective bridging therapy for chemorefractory DLBCL patients eligible for CAR T cells who present with a high tumor burden, including massive BM involvement associated with leukemic involvement. This preliminary evidence is worth confirming in additional patients.
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