Chimeric antigen receptor‐T cell therapy shows similar efficacy and toxicity in patients with diffuse large B‐cell lymphoma aged 70 and older compared to younger patients: A multicenter cohort study

Author:

Berning Philipp1ORCID,Shumilov Evgenii1,Maulhardt Markus2,Boyadzhiev Hristo34,Kerkhoff Andrea1,Call Simon1,Reicherts Christian1,Saidy Anna O.5,Aydilek Enver2ORCID,Hoffmann Michèle3,Novak Urban3,Daskalakis Michael6,Schmitz Norbert1,Stelljes Matthias1,Wulf Gerald2,Bacher Ulrike6,Lenz Georg1,Pabst Thomas3

Affiliation:

1. Department of Hematology and Oncology University Hospital Muenster Muenster Germany

2. Department of Hematology and Medical Oncology University Hospital Göttingen Göttingen Germany

3. Department of Medical Oncology, University Hospital Bern University of Bern Bern Switzerland

4. Habichtswald Hospital Kassel Germany

5. Department of Hematology, Oncology, and Tumor Immunology Helios Klinikum Berlin‐Buch Berlin Germany

6. Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital University of Bern Bern Switzerland

Abstract

AbstractCD19‐directed chimeric antigen receptor (CAR)‐T cell therapy has become a standard treatment for relapsed/refractory diffuse large B‐cell lymphoma (r/r DLBCL). While the benefits of CAR‐T cell treatment are clear in the general patient population, there remains a relative scarcity of real‐world evidence regarding its efficacy and toxicity in patients (pts) aged ≥70 years with DLBCL. We conducted a multicenter retrospective analysis including 172 r/r DLBCL pts with CAR‐T cell treatment, axicabtagene ciloleucel or tisagenlecleucel, between 2019 and 2023 at three tertiary centers. Pts were grouped by age at CAR‐T infusion (<70 vs. ≥70 years). Subsequently, descriptive and survival analyses, including propensity score matching, were performed to compare outcomes between both age groups. We identified 109 pts aged <70 and 63 pts aged ≥70 years. Overall response rates for both age groups were comparable (77.7% vs. 78.3%; p = 0.63). With a median follow‐up of 8.3 months, median progression‐free survival was 10.2 months (95% confidence interval [CI]: 6.5–21.8) and 11.1 months (95% CI: 4.9–NR) (p = 0.93) for both cohorts. Median overall survival reached 21.8 months (95% CI: 11.8–NR) and 34.4 months (95% CI: 10.1–NR) (p = 0.97), respectively. No significant differences in the incidence of cytokine release syndrome (p = 0.53) or grade ≥3 neurotoxicity (p = 0.56) were observed. Relapse and nonrelapse mortality were not significantly different between both groups. Our findings provide additional support that CAR‐T cell therapy is feasible and effective in patients with r/r DLBCL aged 70 years or older, demonstrating outcomes comparable to those observed in younger patients. CAR‐T cell therapy should be not withheld for elderly patients with r/r DLBCL.

Publisher

Wiley

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