European journal of haematology
October 7, 2026 · via Europe PMC
BCMA-Targeted Immunotherapy in Early Relapsed/Refractory Multiple Myeloma: Mechanisms, Clinical Evidence, and Practical Management.
Martino M, Bilardi E, Pitea M, +6 more, Alati C
AI summary — for doctors, generated from the abstract only
BCMA-directed therapies are reshaping early relapsed myeloma, with CAR-T less effective after prior BCMA bispecific exposure than the reverse.
What was studied
Comparative narrative review of pivotal phase II-III trials of belantamab, BCMA bispecifics and BCMA CAR-T in early relapsed/refractory myeloma.
Key findings
- MajesTEC-3 teclistamab-daratumumab 36-month PFS 83.4% vs 29.7%; CARTITUDE-4 cilta-cel median PFS not reached vs 11.8 months
- DREAMM-7/8 belantamab regimens had modest MRD negativity (24.7% for DREAMM-7)
- Prior BCMA bispecific exposure compromises CAR-T efficacy
Clinical relevance
Highlights sequencing and the need for competency in managing ADC, bispecific and CAR-T toxicities.
Who should care
Limitations
Narrative review comparing different trial populations, so cross-trial comparisons are indirect.
Plan sequencing deliberately and be familiar with class-specific toxicities.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
BACKGROUND
B-cell maturation antigen (BCMA), a plasma cell-restricted member of the tumor necrosis factor receptor superfamily, has emerged as the premier immunotherapeutic target in Multiple Myeloma (MM).
METHODS
We performed a comprehensive, comparative review of pivotal Phase II and III clinical trials of BCMA-directed therapies, including the antibody-drug conjugate (ADC) belantamab mafodotin (belamaf), bispecific antibodies (BsAbs), and BCMA-directed chimeric antigen receptor T-cell (CAR-T) products, with explicit attention to balanced, platform-by-platform comparison of efficacy, durability, toxicity, and sequencing evidence rather than emphasis on a single agent.
RESULTS
BCMA-directed therapies deliver unprecedented benefit in early relapse settings. DREAMM-7 established belamaf plus bortezomib-dexamethasone (BVd) as a new reference point, and DREAMM-8 showed benefit for belamaf plus pomalidomide-dexamethasone (BPd), although both regimens achieved comparatively modest MRD-negativity rates (24.7% and pending, respectively) relative to CAR-T and emerging BsAb combinations, and depth of response requires further maturation. MajesTEC-3 showed teclistamab plus daratumumab achieved a 36-month PFS rate of 83.4%, compared with 29.7% for daratumumab-based triplets. CARTITUDE-4 showed ciltacabtagene autoleucel produced a median PFS not reached, compared with 11.8 months with standard of care in lenalidomide-refractory patients with 1-3 prior lines, with MRD-negativity of 60.6%. Sequencing data indicate an asymmetric effect: CAR-T efficacy is substantially compromised by prior BCMA-directed BsAb exposure, whereas BsAbs largely retain meaningful activity after prior BCMA-directed CAR-T.
CONCLUSIONS
BCMA-directed therapies are rapidly redefining early R/R MM treatment. Optimal sequencing, management of class-specific toxicities-including immune effector cell-associated hemophagocytic lymphohistiocytosis-like syndrome (IEC-HS), enterocolitis (IEC-EC), and hematotoxicity (ICAHT), in addition to CRS and ICANS-and inclusion in current guidelines require hematologists to develop competency across ADC, BsAb, and CAR-T platforms. Future directions include advancing BCMA therapies into frontline settings, next-generation and in vivo/allogeneic CAR-T approaches, and exploring novel combination strategies.
DOI
10.1111/ejh.70328
PMID
42841179
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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