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ASH 2025 | The incidence of CNS relapse after CAR T-cell therapy for R/R large B-cell lymphoma

Gloria Iacoboni, MD, PhD, Vall d’Hebron Institute of Oncology, Barcelona, Spain, discusses the low incidence of central nervous system (CNS) relapse after CAR T-cell therapy in patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL), highlighting that a recent analysis found the risk to be similar to that observed with chemoimmunotherapy. This interview took place at the 67th ASH Annual Meeting and Exposition, held in Orlando, FL.

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Transcript

Yes, so at this ASH meeting 2025, we have a poster which has been presented on Monday looking at the incidence of CNS relapse after CAR-T cell therapy and patients who had no previous history of CNS involvement. So patients… we excluded patients with primary CNS lymphoma, with secondary CNS infiltration, even patients who had CNS involvement at diagnosis and had cleared that prior to CAR T-cells; those patients were also excluded...

Yes, so at this ASH meeting 2025, we have a poster which has been presented on Monday looking at the incidence of CNS relapse after CAR-T cell therapy and patients who had no previous history of CNS involvement. So patients… we excluded patients with primary CNS lymphoma, with secondary CNS infiltration, even patients who had CNS involvement at diagnosis and had cleared that prior to CAR T-cells; those patients were also excluded. So definitely excluding all patients with any kind of a history of CNS involvement. 

And we eventually had a patient population of a thousand plus patients who had received CAR T-cell therapy, and we observed that the incidence of CNS relapse was indeed very low. Interestingly, we compared this to a chemoimmunotherapy cohort to try and hypothesize that perhaps, as CAR T-cell therapy, CAR T-cells cross the blood-brain barrier, there would be some kind of protective effect from CAR T-cell therapy, even if the patient was relapsing to that treatment, compared to chemoimmunotherapy in the second-line setting with a platinum-based salvage chemoimmunotherapy regimen. However, in this analysis, we observed a similar low risk of CNS relapse, both in the CAR-T-cell therapy cohort and the chemoimmunotherapy cohort. I think, you know, definitely it will be very valuable to see, you know, the first-line CAR T-cell trials, you know, the ZUMA-12 and the ZUMA-23, look at the CNS relapse incidence in these patients, you know, after CAR T-cells, if they relapse, you know, that will definitely shed some additional light on this question. So this will be presented as a poster on Monday, and we’re very excited to share this data with everyone.

 

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