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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:CD19 Directed CAR T Therapy for Transformed Follicular Lymphoma: A CIBMTR Analysis.
CD19 Directed CAR T Therapy for Transformed Follicular Lymphoma: A CIBMTR Analysis.
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。
转化型滤泡性淋巴瘤(tFL)通常与化疗耐药和不良预后相关。关于复发/难治性(R/R)tFL患者接受CD19靶向CAR-T 细胞治疗后的结局,目前数据有限。在国际血液和骨髓移植研究中心注册库中,共识别出923例在2017年至2023年间接受商业化CD19 CAR-T 治疗的R/R tFL成人患者。中位年龄为64岁(范围:30-86),中位既往治疗线数为4(范围:1-18)。大多数患者(78%)接受了axicabtagene ciloleucel,67%的患者在CAR-T 输注时存在耐药性疾病。
从CAR-T 输注起中位随访25个月(范围:1-72),2年总生存期(OS)率为57%(95% CI:53-60),无进展生存期(PFS)率为43%(95% CI:40-47)。2年复发或进展(rel/prog)及非复发死亡(NRM)的累积发生率分别为47%(95% CI:44-51)和9%(95% CI:7-11)。CAR-T 的总体缓解率为76%,完全缓解率为63%。7.1%的患者观察到3级细胞因子释放综合征(CRS),21.6%的患者观察到3级免疫效应细胞相关神经毒性综合征(ICANS)。多变量分析提示,CAR-T 时存在耐药性疾病状态、使用桥接治疗以及高合并症指数3与较差的PFS和OS相关。年龄60岁以上显著增加了NRM风险。我们的研究表明,CD19 CAR-T 对tFL有效且安全。
Transformed follicular lymphoma (tFL) is typically associated with chemotherapy resistance and a poor prognosis. There are limited data regarding outcomes after CD19-directed chimeric antigen receptor T-cell (CAR T) therapy in relapsed/refractory (R/R) tFL. A total of 923 adult patients with R/R tFL who received commercial CD19 CAR T therapy between 2017 and 2023 were identified in the Center for International Blood and Marrow Transplant Research registry. Median age was 64 years (range: 30-86) and median prior lines of therapy was 4 (range: 1-18). Most patients (78%) received axicabtagene ciloleucel, with 67% of patients having resistant disease at the time of CAR T infusion.
At a median follow-up of 25 months (range: 1-72) from CAR T infusion, the 2-year overall survival (OS) was 57% (95% CI: 53-60) and progression-free survival (PFS) was 43% (95% CI: 40-47). The 2-year cumulative incidences of relapse or progression (rel/prog) and non-relapse mortality (NRM) were 47% (95% CI: 44-51) and 9% (95% CI: 7-11), respectively. The overall response rate to CAR T was 76%, with a complete response rate of 63%.
Grade 3 cytokine release syndrome (CRS) was observed in 7. 1% and grade 3 immune effector cell-associated neurologic syndrome (ICANS) in 21. 6% of patients. Multivariable analysis suggested that resistant disease status at the time of CAR T, use of bridging therapy, and high comorbidity index 3 were associated with inferior PFS and OS. Older age 60 significantly increased the risk of NRM.
Our study suggests that CD19 CAR T is effective and safe for tFL.
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