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Efficacy and Safety Comparisons of Four Approved Chimeric Antigen Receptor T-Cell Therapies in Multiple Myeloma.

Hematological oncology 2026 Vol.44(2) p. e70179

Song Z, Fu Q, Du J

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Despite significant advances in novel therapies, multiple myeloma (MM) remains incurable due to inevitable relapse.

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APA Song Z, Fu Q, Du J (2026). Efficacy and Safety Comparisons of Four Approved Chimeric Antigen Receptor T-Cell Therapies in Multiple Myeloma.. Hematological oncology, 44(2), e70179. https://doi.org/10.1002/hon.70179
MLA Song Z, et al.. "Efficacy and Safety Comparisons of Four Approved Chimeric Antigen Receptor T-Cell Therapies in Multiple Myeloma.." Hematological oncology, vol. 44, no. 2, 2026, pp. e70179.
PMID 41721717
DOI 10.1002/hon.70179

Abstract

Despite significant advances in novel therapies, multiple myeloma (MM) remains incurable due to inevitable relapse. Chimeric antigen receptor (CAR) T-cell therapy is an innovative immunotherapy that has demonstrated remarkable efficacy in patients with relapsed/refractory (R/R) MM. To date, four B-cell maturation antigen (BCMA)-targeting CAR T-cell therapies have been approved in the United States and China for the treatment of R/R MM: idecabtagene vicleucel, ciltacabtagene autoleucel, equecabtagene autoleucel, and zevorcabtagene autoleucel. Although these four CAR T-cell therapies have achieved encouraging response rates in R/R MM, a comprehensive comparative analysis of their efficacy and toxicity profiles is still lacking. In this review, we compare the efficacy and safety of these four approved BCMA-directed CAR T-cell therapies. We also discuss potential factors underlying the observed differences and highlight strategies that may further improve the clinical outcomes of this revolutionary therapy.

MeSH Terms

Humans; Multiple Myeloma; Immunotherapy, Adoptive; Receptors, Chimeric Antigen; B-Cell Maturation Antigen

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