Evidence map›Paper›PMID 42020379›Full record

ArticleBlood cancer journal2026

Validation and refinement of the new Consensus Genomic Staging (CGS) of high-risk multiple myeloma (HRMM) in relapsed and refractory patients treated with BCMA CAR-T.

Joshua N Gustine, Narsis Attar, Benjamin R Puliafito, Diana D Cirstea, Andrew R Branagan, Andrew J Yee, Noopur S Raje

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Article in Blood cancer journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Joshua N GustineMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA, USA.ORCID 0009-0008-8300-1266
Narsis AttarMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA, USA.
Benjamin R PuliafitoMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA, USA.
Diana D CirsteaMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA, USA.
Andrew R BranaganMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-3868-9267
Andrew J YeeMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-3623-7491
Noopur S RajeMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA, USA. nraje@mgh.harvard.edu.ORCID 0000-0003-3066-1275

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The new Consensus Genomic Staging (CGS) of high-risk multiple myeloma (MM) was recently updated by the International Myeloma Society and International Myeloma Working Group. We performed a retrospective study to validate the revised HRMM criteria in relapsed and refractory MM patients treated with BCMA CAR-T. A total of 158 patients were included, of whom 75 (47%) met criteria for HRMM. The median follow-up was 24.8 months (95% CI 22.5-30.3). On multivariable analysis, patients with HRMM had significantly shorter PFS (HR 1.89, p = 0.003) and OS (HR 3.06, p < 0.001) compared to standard-risk MM (SRMM) following BCMA CAR-T. LDH > 210 U/L and EMD were also identified as independent adverse risk factors. Based on survival analyses, we constructed a reclassified staging system incorporating LDH and EMD into the CGS-HRMM criteria. Patients were divided into four discrete risk groups: low risk (SRMM with normal LDH and no EMD; n = 42, 26%), intermediate-low risk (HRMM with normal LDH and no EMD; n = 31, 20%), intermediate-high risk (SRMM with high LDH, EMD, or both; n = 41, 26%), and high risk (HRMM with high LDH, EMD, or both; n = 44, 28%). Patients with low, intermediate-low, intermediate-high, and high-risk disease had a median PFS of 35.0, 19.6, 10.4, and 6.6 months, respectively (p < 0.0001), and an estimated 24-month OS of 90%, 69%, 66%, and 26%, respectively (p < 0.0001). In summary, we validated the new CGS-HRMM criteria in relapsed and refractory MM patients treated with BCMA CAR-T. We also propose a reclassified staging system to further improve risk stratification in MM patients treated with BCMA CAR-T.

Indexed as

B-Cell Maturation AntigenImmunotherapy, AdoptiveMultiple MyelomaAdultAgedAged, 80 and overFemaleGenomicsHumansMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingRetrospective StudiesB-Cell Maturation Antigen

Identifiers

PMID42020379
PMCPMC13233846

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.