Sequencing BCMA-Directed Therapies in Relapsed/Refractory Multiple Myeloma: A Real-World Comparison of CAR T-Cell Therapy and Bispecific Antibodies
Background: Several B-cell maturation antigen (BCMA)-directed therapy (BDT) modalities have been approved by the US Food and Drug Administration (FDA) for relapsed-refractory multiple myeloma (RRMM). Ideal sequencing of these therapies remains unknown. Methods: We report one of the largest multicenter retrospective patient cohorts in this real-world analysis of patients receiving a BDT in both BDT-naïve and exposed settings at major academic centers. Results: In the BDT-naïve setting, which included 276 patients, 169 (61%) received chimeric antigen receptor T-cell therapy (CAR-T), whereas 107 (39%) received bispecific antibodies (BsAbs). Median progression-free survival (PFS) in the BDT-naïve setting was significantly longer with CAR-T than with BsAbs (16.1 vs. 13.5 months, p = 0.007) with a higher overall response rate (ORR) (87 vs. 68%). Multivariable Cox regression analysis revealed that receiving CAR-T (hazard ratio [HR] = 0.41), cytokine release syndrome (CRS) of any grade (HR = 0.50), achieving a best response of ≥very good partial response (VGPR) (HR = 0.12), and high-risk cytogenetic abnormalities (HRCA) (HR = 2.29) were all significant prognostic indicators of PFS. Similarly, HRCA (HR = 2.32), CRS (HR = 0.36), and a best response of ≥VGPR (HR = 0.16) were all independent prognostic factors of overall survival (OS). Of the 80 patients who received prior BDT, 22 received CAR-T (28%) and 58 (72%) received BsAbs. The median PFS was 6.3 months in the CAR-T group, with 64% ORR, vs. 4.4 months in the BsAb group, with 53% ORR (PFS HR, 0.93). Only the best response, ≥VGPR (HR = 0.20), achieved significance in the multivariable model. Conclusions: CAR-T led to more durable responses in the BDT-naïve setting than BsAbs. Responses to either modality were weaker in the BDT-exposed setting. These results highlight the importance of sequencing BDT in RRMM.
Authors
- Mansi R. Shah (ORCID: https://orcid.org/0000-0001-8884-3085)
- Christopher Sun Strouse (ORCID: https://orcid.org/0000-0003-4964-167X)
- Abdullah Khan (ORCID: https://orcid.org/0000-0003-2166-2583)
- Zahra Mahmoudjafari (ORCID: https://orcid.org/0000-0002-3168-2521)
- Jeries Kort (ORCID: https://orcid.org/0000-0001-9182-3931)
- Al-Ola A. Abdallah (ORCID: https://orcid.org/0000-0002-6603-185X)
- Osama Mustafa Younis (ORCID: https://orcid.org/0009-0004-1027-554X)
- Andrew J. Vegel (ORCID: https://orcid.org/0000-0002-1882-0504)
- Muhammad Umair Mushtaq (ORCID: https://orcid.org/0000-0001-8122-0563)
- Shebli Atrash (ORCID: https://orcid.org/0000-0003-4547-7534)
- Prerna Mewawalla (ORCID: https://orcid.org/0009-0008-7464-6898)
- Emily Struble (ORCID: https://orcid.org/0000-0003-0660-3446)
- Joseph P. McGuirk (ORCID: https://orcid.org/0000-0002-0539-4796)
- Omar Abed Alkharabsheh (ORCID: https://orcid.org/0000-0002-5299-4233)
- Abhiraj Saxena (ORCID: https://orcid.org/0009-0009-7338-2269)
- Jordan Andrew Snyder (ORCID: https://orcid.org/0000-0002-1001-134X)
- Hira Ghazal Shaikh (ORCID: https://orcid.org/0000-0001-5604-4166)
- Sencer Göklemez (ORCID: https://orcid.org/0000-0002-0487-2426)
- Anita Mazloom (ORCID: https://orcid.org/0009-0009-7899-7078)
- Barry A. Paul (ORCID: https://orcid.org/0000-0003-2702-8225)
- Alma Habib (ORCID: https://orcid.org/0000-0003-4429-3602)
- Carmel Awadallah
Institutions
- University of Jordan (JO)
- University of Iowa (US)
- Allegheny Health Network (US)
- USA Mitchell Cancer Institute (US)
- St. Luke's Episcopal Hospital (US)
- University of Kansas Medical Center (US)
- Rutgers Cancer Institute (US)
- Wake Forest University (US)
- The Ohio State University (US)
- University of Cincinnati (US)
Publication Details
- Journal
- Cancers
- Published
- 2026-09-29
- DOI
- https://doi.org/10.3390/cancers18193147
- Primary Topic
- CAR-T cell therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00