Thiruvengadam Swetha Kambhampati, Ahn Kwang Woo, Patel Jinalben, Lian Qinghua, Hertzberg Mark, Epperla Narendranath, Metheny Leland, Hong Sanghee, Jain Tania, Aljurf Mahmoud, Beitinjaneh Amer, Vaughn John, Gopal Ajay, Iqbal Madiha, Wirk Baldeep, Manjappa Shivaprasad, Oliver Carolina, Mohty Razan, Shadman Mazyar, Turtle Cameron, Hamadani Mehdi, Herrera Alex F
Department of Hematology and Hematopoietic Stem Cell Transplantation, City of Hope National Medical Center, Duarte, California, USA.
Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Am J Hematol. 2025 Oct;100(10):1803-1812. doi: 10.1002/ajh.70027. Epub 2025 Aug 5.
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.
转化型滤泡性淋巴瘤(tFL)通常与化疗耐药及预后不良相关。关于复发/难治性(R/R)tFL患者接受靶向CD19嵌合抗原受体T细胞(CAR T)治疗后的预后数据有限。国际血液和骨髓移植研究中心登记处识别出了2017年至2023年间共923例接受商业化CD19 CAR T治疗的R/R tFL成年患者。中位年龄为64岁(范围:30 - 86岁),既往治疗的中位疗程数为4个(范围:1 - 18个)。大多数患者(78%)接受了阿基仑赛注射液,67%的患者在接受CAR T输注时患有耐药性疾病。自CAR T输注起,中位随访25个月(范围:1 - 72个月),2年总生存率(OS)为57%(95%置信区间:53 - 60),无进展生存率(PFS)为43%(95%置信区间:40 - 47)。2年复发或进展(rel/prog)及非复发死亡率(NRM)的累积发生率分别为47%(95%置信区间:44 - 51)和9%(95%置信区间:7 - 11)。CAR T的总体缓解率为76%,完全缓解率为63%。7.1%的患者出现≥3级细胞因子释放综合征(CRS),21.6%的患者出现≥3级免疫效应细胞相关神经综合征(ICANS)。多变量分析表明,CAR T治疗时的耐药疾病状态、桥接治疗的使用以及高合并症指数≥3与较差的PFS和OS相关。年龄≥60岁显著增加了NRM风险。我们的研究表明,CD19 CAR T治疗tFL有效且安全。