Outcomes of CD19 CAR-T therapy in central nervous system lymphoma: Insights from a multicentre experience Journal Article


Authors: Cassanello, G.; Luttwak, E.; Brown, S.; Devlin, S. M.; Imber, B.; Ip, A.; Leslie, L. A.; Accav, N. G.; Avigdor, A.; Marcus, R.; Beyar-Katz, O.; Corona, M.; Luna De Abia, A.; Calabrese De Feo, J.; Rivas Delgado, A.; Lue, J. K.; Grommes, C.; Shah, G. L.; Park, J.; Perales, M. A.; Salles, G.; Shouval, R.; Scordo, M.; Palomba, M. L.
Article Title: Outcomes of CD19 CAR-T therapy in central nervous system lymphoma: Insights from a multicentre experience
Abstract: Chimeric antigen receptor (CAR) T-cell therapy has reshaped the treatment paradigm for relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL). However, its role in central nervous system lymphoma (CNSL) remains uncertain. We conducted a multicentre, retrospective study on 54 adult R/R CNSL patients treated at four international institutions with commercial (axi-cel, tisa-cel, liso-cel) or a point of care (POC) CD19-CAR T-cell products. At day 100 post CAR-T infusion, 65% of patients attained a complete response as their best response in both systemic and central nervous system compartments. The median progression-free survival (PFS) was 7.5 months, with a 1-year PFS of 35%. The median overall survival (OS) was 19 months, with a 1-year OS of 63%. In multivariable analyses, CAR-T product was significantly associated with PFS (p = 0.009) and OS (p = 0.013), with patients receiving tisa-cel exhibiting poorer outcomes than axi-cel and patients receiving liso-cel or POC CAR-T product demonstrating better outcomes than axi-cel. Toxicity profiles were consistent with pivotal trials in R/R DLBCL. Grade ≥3 cytokine release syndrome occurred in 11% of patients, while grade ≥3 immune-effector cell-associated neurotoxicity syndrome was observed in 28%. Our study supports the feasibility and safety of anti-CD19 CAR-T therapy in CNSL. The specific CAR-T product infused emerged as a factor influencing outcomes. © 2025 British Society for Haematology and John Wiley & Sons Ltd.
Keywords: immunotherapy; lymphoma; cellular therapies; haematological oncology
Journal Title: British Journal of Haematology
ISSN: 0007-1048
Publisher: John Wiley & Sons  
Publication status: Online ahead of print
Date Published: 2025-07-01
Online Publication Date: 2025-07-01
Language: English
DOI: 10.1111/bjh.20234
PROVIDER: scopus
PUBMED: 40589238
DOI/URL:
Notes: Article -- MSK Cancer Center Support Grant (P30 CA008748) acknowledged in PubMed and PDF -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics