Evidence map›Paper›PMID 42458324›Full record

ArticleBMC cancer2026

Validation and prognostic utility of the mSMART 4.0 risk stratification system in Chinese patients with multiple myeloma.

Jian Yin, Rui Liu, Yanping Zhang, Zeshi Liu, Yangyang Gong, Aili He

Abstract readValidation Study
In one paragraph

Article in BMC cancer, 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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5 · Who and what money

Authors and funding

6 authors.

Jian YinDepartment of Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004, China.
Rui LiuDepartment of Hematology, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157 West Five Road, Xi'an, Shaanxi, 710004, China. sszhu250@stu.xjtu.edu.cn.
Yanping ZhangDepartment of Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004, China.
Zeshi LiuDepartment of Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004, China.
Yangyang GongDepartment of Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710004, China.
Aili HeDepartment of Hematology, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157 West Five Road, Xi'an, Shaanxi, 710004, China. heaili@xjtu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe 2024 Mayo Clinic mSMART 4.0 risk stratification system features significant revisions, yet its utility in Chinese multiple myeloma (MM) patients remains unvalidated. This study evaluates its prognostic performance in a Chinese cohort.

methodsWe retrospectively collected clinical data from newly diagnosed MM (NDMM) patients and followed them up. Clinical characteristics, therapeutic responses, and survival were compared between high-risk and standard-risk groups defined by mSMART 4.0. Harrell's concordance index (C-index) analysis was used to compare the predictive efficacy of mSMART 4.0 versus version 3.0.

resultsAmong 202 patients, 69 (34.2%) were high-risk according to mSMART 4.0. The mSMART 4.0 high-risk group demonstrated significantly lower deep response rates, alongside shorter median PFS (P < 0.001) and OS (P < 0.001). The proportion of the high-risk group was lower under mSMART 4.0 (34.2%) compared to mSMART 3.0 (51.9%). C-index revealed that mSMART 4.0 possessed superior prognostic predictive validity (C-index = 0.738, 95% CI: 0.677-0.792) relative to mSMART 3.0 (C-index = 0.572, 95% CI: 0.490-0.649). The increase in the C-index was statistically significant (ΔC-index = 0.167, 95% CI: 0.065-0.269, P = 0.003). Multivariate analysis identified mSMART 4.0 high-risk status as an independent adverse prognostic factor for both PFS (HR = 2.027; 95% CI: 1.364-3.012) and OS (HR = 5.352; 95% CI: 2.794-10.250). Additionally, elevated lactate dehydrogenase (LDH) was an independent predictor of poor PFS (HR = 1.002; 95% CI: 1.001-1.004).

conclusionIn this Chinese cohort, mSMART 4.0 effectively stratifies multiple myeloma patients and serves as an independent predictor of inferior prognosis, demonstrating superior prognostic value over version 3.0.

Indexed as

Multiple MyelomaAdultAgedAged, 80 and overChinaEast Asian PeopleFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesRisk AssessmentClinical characteristicsmSMART 3.0mSMART 4.0Multiple myelomaPrognosis

Identifiers

PMID42458324
PMCPMC13678907

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