Comparative survival and time toxicity outcomes of CAR-T versus bispecific antibody therapies in relapsed/refractory FL

Chimeric antigen receptor T-cell (CAR-T) and CD20xCD3 bispecific antibody (BsAb) therapies are both effective for relapsed/refractory (R/R) follicular lymphoma (FL), but comparative real-world survival outcomes and time toxicity have not been characterized. We performed a multicenter retrospective study of 228 patients with R/R FL treated with standard-of-care CAR-T (n = 141) or BsAb (n = 87) across 17 U.S. academic centers in the third-line or later setting. Progression-free survival (PFS) and overall survival (OS) were stratified by 2 or ≥3 prior lines of therapy (LOT2 or LOT3+), including propensity matching. Time toxicity was measured by physical health care contact days. Median PFS was not reached (NR) with CAR-T and 581 days with BsAb in the LOT2 cohort (p < .0001), and was NR with CAR-T and 584 days with BsAb in the LOT3+ cohort (p = .0064). CAR-T recipients were younger (p < .0001) and had better performance status (p = .007) but were more refractory to prior LOT (p = .017). PFS advantages of CAR-T were independent of these differences. OS did not differ between treatment groups. CAR-T had significantly greater time toxicity over the first year, with higher mean contact days than BsAb in both the LOT2 (58 vs 44) and LOT3+ (69 vs 49) cohorts. In this large multicenter cohort of patients with R/R FL, CAR-T was associated with superior PFS but greater time toxicity compared with BsAb therapy. These findings provide real-world outcomes data and time toxicity benchmarks to support treatment sequencing decision-making in R/R FL.

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Publication Details

Journal
Blood Advances
Published
2026-10-30
DOI
https://doi.org/10.1182/bloodadvances.2026020899
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Comparative survival and time toxicity outcomes of CAR-T versus bispecific antibody therapies in relapsed/refractory FL

Reem Karmali, Hua-Jay Jeffery Cherng, Nicole Altomare, Danielle S. Wallace et al.
6 links
Blood Advances
CAR-T cell therapy research
article

Comparative survival and time toxicity outcomes of CAR-T versus bispecific antibody therapies in relapsed/refractory FL

Reem Karmali, Hua-Jay Jeffery Cherng, Nicole Altomare, Danielle S. Wallace, Brian Thomas Hill, Arjab Adhikari, Mazie Tsang, Danny Trotier, Edd Ricker, Arjun Gupta, Jose Caetano Villasboas, Dilan Anil Patel, Allison Marie Bock, Taylor Brooks, Pallawi Torka, Christopher Mwaniki Wanjiku, Madiha Iqbal, Jennifer C. Keenan, Jonathan Harry Schatz, Asaad Trabolsi, Jordan Andrew Snyder, Ajay Major, Samin Houshyar, Charlotte Burton Wagner, Priyanka Avinash Pophali, Timothy J. Voorhees, Nausheen Ahmed, Supriya Gupta, Nidhi Desai, Diana Abbott, John Sharp, Jessica A. Chicola, Haya Al Any, Mohamed Rajab, Alline Nogueira Serodio
article en

Abstract

Chimeric antigen receptor T-cell (CAR-T) and CD20xCD3 bispecific antibody (BsAb) therapies are both effective for relapsed/refractory (R/R) follicular lymphoma (FL), but comparative real-world survival outcomes and time toxicity have not been characterized. We performed a multicenter retrospective study of 228 patients with R/R FL treated with standard-of-care CAR-T (n = 141) or BsAb (n = 87) across 17 U.S. academic centers in the third-line or later setting. Progression-free survival (PFS) and overall survival (OS) were stratified by 2 or ≥3 prior lines of therapy (LOT2 or LOT3+), including propensity matching. Time toxicity was measured by physical health care contact days. Median PFS was not reached (NR) with CAR-T and 581 days with BsAb in the LOT2 cohort (p < .0001), and was NR with CAR-T and 584 days with BsAb in the LOT3+ cohort (p = .0064). CAR-T recipients were younger (p < .0001) and had better performance status (p = .007) but were more refractory to prior LOT (p = .017). PFS advantages of CAR-T were independent of these differences. OS did not differ between treatment groups. CAR-T had significantly greater time toxicity over the first year, with higher mean contact days than BsAb in both the LOT2 (58 vs 44) and LOT3+ (69 vs 49) cohorts. In this large multicenter cohort of patients with R/R FL, CAR-T was associated with superior PFS but greater time toxicity compared with BsAb therapy. These findings provide real-world outcomes data and time toxicity benchmarks to support treatment sequencing decision-making in R/R FL.

Blood Advances
Northwestern University (US), City Of Hope National Medical Center (US), University of Minnesota (US), Cleveland Clinic (US), Mayo Clinic (US), Memorial Sloan Kettering Cancer Center (US), University of Wisconsin–Madison (US), University of Miami (US), University of Kansas (US), Colorado School of Public Health (US), Oregon Health & Science University (US), Washington University in St. Louis (US), Columbia University Irving Medical Center (US), Ochsner Medical Center (US), Huntsman Cancer Institute (US), University of Rochester Medical Center (US), The University of Kansas Cancer Center (US), University of Wisconsin Carbone Cancer Center (US), City of Hope (US), Mayo Clinic Hospital (US), Mayo Clinic in Florida (US), UNC Lineberger Comprehensive Cancer Center (US), Masonic Cancer Center (US), Cleveland Clinic Abu Dhabi (AE), University of Colorado Anschutz Medical Campus (US), The Ohio State University (US), University of Colorado Denver (US)
Incyte, Genentech
Good health and well-being
Openalex Percentile: Top 16%
CAR-T cell therapy research
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