Inferior survival in double refractory large B-cell lymphoma eligible for third-line CD19 CAR T-cell therapy

Outcomes following CD19 chimeric antigen receptor (CAR) T-cell therapy in third-line treatment and beyond for patients with large B-cell lymphoma (LBCL) refractory to both an anthracycline during initial and platinum-based salvage therapy, referred to as double refractory (DR), are not well-described. It is also unclear if these patients may be less likely to proceed to CAR T-cell infusion. Our objectives were to assess third-line CAR T-cell survival outcomes in DR- and non-DR (NDR)-LBCL cohorts including the failure rates to proceed to cell infusion. Review of 199 patients with LBCL referred for CAR T-cell treatment at our center, demonstrates that the DR-LBCL patients (n = 68) have an inferior 12-month (overall survival [OS], 47.1% vs 66.7%, respectively;) when compared to the patients with NDR-LBCL (n = 131). This OS difference is driven by a higher failure rate to proceed to CAR T-cell infusion (32% vs 18%). For patients unable to proceed to CAR T-cell infusion median OS was 2.56 months; DR-LBCL 1.94 months vs NDR-LBCL 3.42 months. The 12-month OS (65% vs 72.3%) and 6-month progression-free survival (46.5% vs 57.2%) of patients with DR- and NDR-LBCL proceeding to CAR T-cell infusion, appears similar. Our study highlights a high-risk subgroup characterized by inferior OS with challenges in getting to CAR T-cell infusion and could benefit from different management approaches such as novel bridging or "off-the-shelf" strategies.

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Publication Details

Journal
Blood Neoplasia
Published
2025-09-01
DOI
https://doi.org/10.1016/j.bneo.2025.100164
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
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article

Inferior survival in double refractory large B-cell lymphoma eligible for third-line CD19 CAR T-cell therapy

Carmel Waldron, Richard Tsang, David Hodgson, Danielle Rodin et al.
Blood Neoplasia
CAR-T cell therapy research
article

Inferior survival in double refractory large B-cell lymphoma eligible for third-line CD19 CAR T-cell therapy

Carmel Waldron, Richard Tsang, David Hodgson, Danielle Rodin, Anca A. Prica, Chathuri Abeyakoon, Robert Kridel, Katrina Hueniken, Nauman Malik, Michael Crump, Vishal Kukreti, Sita Bhella, Rachel Aitken, Abi Vijenthira, John Kuruvilla, Woodrow Wells, Christine Chen, Jing Yang
article en

Abstract

Outcomes following CD19 chimeric antigen receptor (CAR) T-cell therapy in third-line treatment and beyond for patients with large B-cell lymphoma (LBCL) refractory to both an anthracycline during initial and platinum-based salvage therapy, referred to as double refractory (DR), are not well-described. It is also unclear if these patients may be less likely to proceed to CAR T-cell infusion. Our objectives were to assess third-line CAR T-cell survival outcomes in DR- and non-DR (NDR)-LBCL cohorts including the failure rates to proceed to cell infusion. Review of 199 patients with LBCL referred for CAR T-cell treatment at our center, demonstrates that the DR-LBCL patients (n = 68) have an inferior 12-month (overall survival [OS], 47.1% vs 66.7%, respectively;) when compared to the patients with NDR-LBCL (n = 131). This OS difference is driven by a higher failure rate to proceed to CAR T-cell infusion (32% vs 18%). For patients unable to proceed to CAR T-cell infusion median OS was 2.56 months; DR-LBCL 1.94 months vs NDR-LBCL 3.42 months. The 12-month OS (65% vs 72.3%) and 6-month progression-free survival (46.5% vs 57.2%) of patients with DR- and NDR-LBCL proceeding to CAR T-cell infusion, appears similar. Our study highlights a high-risk subgroup characterized by inferior OS with challenges in getting to CAR T-cell infusion and could benefit from different management approaches such as novel bridging or "off-the-shelf" strategies.

Blood NeoplasiaVol. 2(4)
University Health Network (CA), University of Toronto (CA), Princess Margaret Cancer Centre (CA)
Openalex Percentile: Top 68%
CAR-T cell therapy research
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