American journal of hematology · 2025
CD19 Directed CAR T Therapy for Transformed Follicular Lymphoma: A CIBMTR Analysis.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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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
Аннотация
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.