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:Treatments of Ph-like acute lymphoblastic leukemia: a real-world retrospective analysis from a single large center in China.
Treatments of Ph-like acute lymphoblastic leukemia: a real-world retrospective analysis from a single large center in China.
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费城染色体样急性淋巴细胞白血病(Ph样ALL)是ALL的一种高危亚型。本研究回顾性分析70例Ph样ALL患者,是目前该白血病CAR-T 细胞治疗和单倍体相合造血干细胞移植(haplo-HSCT)规模最大的研究。患者中位年龄26岁,中位白细胞计数31.44×10⁹/L。接受化疗、激酶抑制剂(KI)、CAR-T 细胞及异基因HSCT的患者比例分别为19%、30%、46%和61%。KI联合化疗治疗1个月后、CAR-T 治疗后及异基因HSCT后的总缓解率分别为62%、73%和100%。5年无病生存期(DFS)和总生存期(OS)分别为35%和51%;5年累积复发率和非复发死亡率分别为63%和11%。单变量分析显示,异基因HSCT与更好的DFS(P=0.010)和OS(P=0.000)相关。综上,在KI基础上联合化疗或CAR-T 后进行异基因HSCT,是治疗Ph样ALL安全且可行的方法。
Philadelphia chromosome-like acute lymphoblastic leukemia (Ph-like ALL) is a high-risk subtype of ALL.
We retrospectively studied 70 cases with Ph-like ALL and here present the largest study of CAR-T cell treatment and haplo-HSCT for this leukemia. Median age was 26 years and median leukocyte count was 31. 44 10 9 /L. The proportion of patients receiving chemotherapy, KIs, CAR-T cells, and allo-HSCT was 19%, 30%, 46%, and 61%, respectively.
The overall response rate was 62%, 73%, and 100% after one month of KI treatment combined with chemotherapy, CAR-T cell therapy, and allo-HSCT, respectively. Five-year DFS and OS were 35% and 51%, respectively. The five-year cumulative incidence of relapse and non-relapse mortality was 63% and 11%, respectively. Allo-HSCT was associated with a better DFS ( p = 0. 010) and OS ( p = 0. 000) by univariate analysis.
In conclusion, allo-HSCT after KIs together with chemotherapy or CAR-T cell therapy is a safe and feasible treatment modality for Ph-like ALL.
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