Extramedullary disease but not paraskeletal disease portends inferior outcomes after CAR T cell therapy in multiple myeloma
- PMID: 40319194
- DOI: 10.1038/s41409-025-02593-3
Extramedullary disease but not paraskeletal disease portends inferior outcomes after CAR T cell therapy in multiple myeloma
Abstract
Chimeric antigen receptor (CAR) T cell therapy is effective for multiple myeloma (MM), yet patients with plasmacytomas, either paraskeletal disease (PSD) or extramedullary disease (EMD), have poorer outcomes. To better distinguish the effects of EMD and PSD on outcomes, we conducted a single-center, retrospective study of 134 relapsed/refractory MM patients treated with CAR T cells. With a median follow-up of 30.2 months, patients with EMD (n = 34) had significantly worse progression-free survival (PFS) and overall survival (OS) than those with bone marrow-only disease (n = 75): PFS was 24.2 months vs. 9.0 months (HR 2.15, 95% CI 1.31-3.54), and OS was not reached vs. 24.0 months (HR 3.79, 95% CI 1.81-7.94). In contrast, patients with PSD did not experience significantly shorter PFS or OS. Among patients with EMD, those with high extramedullary tumor burden had a lower overall response rate (ORR). For extramedullary tumor burden <25 cm2, 25-50 cm2, and >50 cm2, ORR was 81.0% (66.7% complete response, CR), 83.3% (50% CR), and 57.1% (0% CR), respectively. Importantly, EMD-positive relapses post-CAR T cell therapy comprised half of all relapses observed. In summary, our findings indicate that EMD, but not PSD, is strongly associated with poor outcomes with CAR T cell therapy.
© 2025. The Author(s), under exclusive licence to Springer Nature Limited.
Conflict of interest statement
Competing interests: DP: Honoraria from Sanofi. THM: Advisory board fees for Sanofi. JR: Consultant/advisory board: Janssen, BMS, Pfizer, Karyopharm, Sanofi, Takeda, Genentech, Abbvie, Regeneron, Forus, Menarini, Speakers Bureau: Janssen, BMS, Sanofi, Adaptive Biotechnologies. SP: Advisory board for Grail; research support from Celgene/BMS Corporation, Grail, Caribou. SJ: Consulting for Janssen Pharmaceuticals, BMS, Caribou Biosciences, Legend Biotech, Regeneron Pharmaceuticals, Takeda Pharmaceuticals, Sanofi, Poseida Therapeutics; Advisory board for Janssen Pharmaceuticals, BMS, GSK; Data Safety Monitoring Board for Janssen Pharmaceuticals, Sanofi, Genmab. LJS: Consulting/advisory board for Janssen Pharmaceuticals. CR: Advisory board for Janssen Pharmaceuticals, Takeda Pharmaceuticals, BMS, Amgen, Karyopharm Therapeutics. ACR: Consulting for Johnson & Johnson, Adaptive, BMS, Sanofi. HJC: Employment: The Multiple Myeloma Research Foundation, Research funding: Genentech/Roche, BMS, Takeda. The remaining authors declare no relevant competing financial interests. Ethics approval: Patient data was retrospectively collected and analyzed in accordance with the Declaration of Helsinki. As many patients were deceased, obtaining informed consent was not possible. Therefore, a waiver of informed consent was granted, and the study was approved by the institutional review board of Mount Sinai (IRB#11-01978-MOD0013).
References
-
- Munshi NC, Anderson LD Jr, Shah N, Madduri D, Berdeja J, Lonial S, et al. Idecabtagene vicleucel in relapsed and refractory multiple myeloma. N Engl J Med. 2021;384:705–16. - PubMed
-
- Berdeja JG, Madduri D, Usmani SZ, Jakubowiak A, Agha M, Cohen AD, et al. Ciltacabtagene autoleucel, a B-cell maturation antigen-directed chimeric antigen receptor T-cell therapy in patients with relapsed or refractory multiple myeloma (CARTITUDE-1): a phase 1b/2 open-label study. Lancet. 2021;398:314–24. - PubMed
-
- Weinstock M, Ghobrial IM. Extramedullary multiple myeloma. Leuk lymphoma. 2013;54:1135–41. - PubMed
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