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:Salvage CD20-SD-CART therapy in aggressive B-cell lymphoma after CD19 CART treatment failure.
Salvage CD20-SD-CART therapy in aggressive B-cell lymphoma after CD19 CART treatment failure.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
CD20-SD-CART 可作为 CD19 CAR-T 治疗失败后复发/难治性侵袭性 B 细胞淋巴瘤患者的有效治疗选择。
回顾纳入2019年12月至2022年5月在北京博仁医院CD19 CAR-T 治疗失败患者,后续接受CD20 CAR-T 或非CAR-T 治疗(含或不含泊洛妥珠单抗)。
93例患者中54例接受CD20 CAR-T。中位随访18.54个月后,与非CAR-T 组相比,CD20 CAR-T 组中位无进展生存期和总生存期更长,完全缓解率也更高。多变量分析证实CD20 CAR-T 与总生存期及无进展生存期改善独立相关。
CD19 CAR-T 失败后的复发/难治性侵袭性B细胞淋巴瘤患者,可考虑CD20靶向CAR-T 作为有效治疗选择。
This retrospective cohort study enrolled patients with aBCL after the failure of CD19 CART treatment at Beijing Gobroad Boren Hospital from December 2019 to May 2022. Patients were subsequently treated with CD20CART therapy or non-CART therapy (polatuzumab or non-polatuzumab).
A total of 93 patients were included in the study, with 54 patients receiving CD20-SD-CART therapy. After a median follow-up of 18.54 months, the CD20-SD-CART group demonstrated significantly longer median progression-free survival (4.04 months vs. 2.27 months, p=0.0032) and median overall survival (8.15 months vs. 3.02 months, p<0.0001) compared to the non-CART group. The complete response rate in the CD20-SD-CART group (15/54, 27.8%) was also significantly higher than the non-CART group (3/38, 7.9%, p=0.03). Multivariate analysis further confirmed that CD20CART treatment was independently associated with improved overall survival (HR, 0.28; 95% CI, 0.16-0.51; p<0.0001) and progression-free survival (HR, 0.46; 95% CI, 0.27-0.8; p=0.005).
CD20-SD-CART could serve as an effective therapeutic option for patients with relapsed or refractory aggressive B-cell lymphoma after CD19CART treatment failure.
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