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

Philipp Berning(University Hospital Münster), Evgenii Shumilov(University Hospital Münster), Markus Maulhardt(Universitätsmedizin Göttingen), Hristo Boyadzhiev(University of Bern), Andrea Kerkhoff(University Hospital Münster), Simon Call(University Hospital Münster), Christian Reicherts(University Hospital Münster), Anna Ossami Saidy(Helios Hospital Berlin-Buch), Enver Aydilek(Universitätsmedizin Göttingen), Michèle J. Hoffmann(University of Bern), Urban Novak(University of Bern), Michael Daskalakis(University of Bern), Norbert Schmitz(University Hospital Münster), Matthias Stelljes(University Hospital Münster), Gerald Wulf(Universitätsmedizin Göttingen), Ulrike Bacher(University of Bern), Georg Lenz(University Hospital Münster), Thomas Pabst(University of Bern)
HemaSphere
March 1, 2024
Cited by 32Open Access
Full Text

Abstract

Abstract CD19‐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.


Related Papers

No related papers found

Powered by citation graph analysis