Chimeric Antigen Receptor T-Cell Therapy for Refractory Multiple Myeloma: A Twenty Four Month Prospective Cohort: Response Rates, Toxicity Profile, and Predictors of Durable Remission

Author
Dr. Ankit Paliwal, Ritu Verma, Dr. Rashmi Sharma
Keywords
Multiple Myeloma; CAR-T Cell Therapy; BCMA; Cytokine Release Syndrome; ICANS; Relapsed Refractory; Idecabtagene; Ciltacabtagene.
Abstract
Chimeric antigen receptor T-cell (CAR-T) therapy targeting B-cell maturation antigen (BCMA) has transformed the treatment of relapsed/refractory multiple myeloma, producing unprecedented response rates in patients with otherwise treatment-resistant disease. Real-world outcomes data from South Asian populations remain limited. We prospectively followed 164 patients infused with anti-BCMA CAR-T therapy (idecabtagene vicleucel or ciltacabtagene autoleucel) at a tertiary cancer centre between 2022 and 2024 over 24 months. Overall response rate was 86.6% with complete or stringent complete response in 35.4%. Median progression-free survival was 11.6 months and 12-month overall survival was 76%. Cytokine release syndrome occurred in 76.8% (grade ≥3 in 13.4%) and ICANS in 37.8% (grade ≥3 in 7.3%). Strongest independent predictors of durable response included achievement of sCR/CR at 3 months, ≤3 prior lines of therapy, absence of extramedullary disease, standard-risk cytogenetics, and high BCMA expression pre-infusion. The findings reproduce trial-level effect sizes in a real-world setting while highlighting infrastructure, cost, and toxicity-management demands of CAR-T programmes.
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Received : 08 May 2026
Accepted : 03 July 2026
Published : 14 July 2026
DOI: 10.30726/esij/v13.i3.2026.1330042

A-38-CART-Myeloma.pdf