Efficacy and safety of frail patients treated with ciltacabtagene autoleucel in the real world: A Center for International Blood and Marrow Transplant Research analysis
BACKGROUND: Ciltacabtagene autoleucel (cilta-cel), an anti-B-cell maturation antigen (BCMA) chimeric antigen receptor T-cell (CAR-T) therapy, is approved for relapsed/refractory multiple myeloma (RRMM). METHODS: Using the Center for International Blood and Marrow Transplant Research registry, this study evaluated outcomes of frail patients receiving commercial cilta-cel from March 2022 to December 2023. Frailty was defined by an adapted simplified score incorporating age, performance status, and comorbidities. RESULTS: Among 541 patients with available frailty status, 183 (33.8%) were frail and 358 (66.2%) were nonfrail. Overall response rates were comparable (frail 82.8% vs. nonfrail 88.5%). However, frail patients had inferior progression-free survival (PFS) (12-month PFS, 62.7% [95% confidence interval (CI), 53.6%-71.3%] vs. 75.9% [95% CI, 70.4%-81.1%]; p < .01) and overall survival (OS) (12-month OS 72.8% [95% CI, 64.9%-80.0%] vs. 90.4% [95% CI, 86.6%-93.7%]; p < .01). Twelve-month treatment-related mortality in frail patients was 6.8% (95% CI, 3.4%-11.2%) versus 3.6% (95% CI, 1.8%-6.1%), p = .12. Cytokine release syndrome (grade ≥2) occurred in 22.4% of frail versus 17.9% of nonfrail patients (p = .05), and immune effector cell-associated neurotoxicity (ICANS) of any grade was reported in 32.2% versus 17.6% (p < .01). Rates of cranial nerve palsies and Parkinsonism were comparable. Prolonged cytopenia (>day 30) was more common in frail patients (30.6% vs. 21.2%; p < .01). On multivariable analysis, frailty independently predicted worse PFS (hazard ratio [HR], 1.67; 95% CI, 1.16-2.40), OS (HR, 2.46; 95% CI, 1.57-3.87), and higher odds of any-grade ICANS (odds ratio, 2.01; 95% CI, 1.32-3.08) (all p < .01). CONCLUSIONS: Cilta-cel remains effective in frail RRMM, but frailty is associated with reduced survival and increased toxicity, supporting tailored CAR-T strategies.
Authors
- Hamza Hashmi (ORCID: https://orcid.org/0000-0002-4129-5867)
- Aimaz Afrough (ORCID: https://orcid.org/0000-0003-2645-8557)
- Heather J. Landau
- Surbhi Sidana (ORCID: https://orcid.org/0000-0003-3288-7614)
- Ashley Elizabeth Rosko (ORCID: https://orcid.org/0000-0001-5875-3214)
- Rahul Kumar Banerjee (ORCID: https://orcid.org/0000-0003-3781-5441)
- Danai Dima (ORCID: https://orcid.org/0000-0002-3587-7975)
- Othman Salim Akhtar (ORCID: https://orcid.org/0000-0003-1673-9670)
- Meera Mohan (ORCID: https://orcid.org/0000-0002-6913-6526)
- Binod Dhakal (ORCID: https://orcid.org/0000-0002-4377-9742)
- Taiga Nishihori (ORCID: https://orcid.org/0000-0002-2621-7924)
- Tiening Chen
- Temitope Oloyede
- Marcelo C. Pasquini (ORCID: https://orcid.org/0000-0003-1579-2293)
- Lohith Gowda (ORCID: https://orcid.org/0009-0001-1726-9749)
- Aram Bidikian
- Hira Mian (ORCID: https://orcid.org/0000-0003-1584-1067)
- Saad Usmani
- Mark Schroeder
- Ajoy Dias
- Lazaros Lekakis
- Jesus Berdeja
- Jakob Devos
- Ravi Narra
- Krina Patel
- Larry D. Anderson
- Nausheen Ahmed
- Doris K. Hansen
- Abu‐Sayeef Mirza
- Ruta Brazauskas
- Muhammad Salman Faisal
- Yvonne A. Efebera
Institutions
- OhioHealth (US)
- Cleveland Clinic (US)
- Memorial Sloan Kettering Cancer Center (US)
- The University of Texas MD Anderson Cancer Center (US)
- University of Miami (US)
- Medical College of Wisconsin (US)
- Washington University in St. Louis (US)
- Juravinski Cancer Centre (CA)
- The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (US)
- Yale Cancer Center (US)
- Moffitt Cancer Center (US)
- Fred Hutch Cancer Center (US)
- Southwestern Medical Center (US)
- Versiti Blood Center of Wisconsin (US)
- University of Kansas Medical Center (US)
- National Cancer Institute (US)
- The University of Texas Southwestern Medical Center (US)
- Stanford University (US)
Publication Details
- Journal
- Cancer
- Published
- 2026-09-24
- DOI
- https://doi.org/10.1002/cncr.70614
- Primary Topic
- CAR-T cell therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00