Evidence map›Paper›PMID 40644760›Full record

ArticleESMO open2025

Quantitative risk of underlying disease conditions for progression from monoclonal gammopathy to multiple myeloma: a nationwide cohort study.

H Ko, S Choi, S-S Park, S Jung, C H Lee, S Han, C-K Min

Abstract read
In one paragraph

Article in ESMO open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

H KoDepartment of Pharmacology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
S ChoiDepartment of Pharmacology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Division of Data Science, PIPET, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
S-S ParkDepartment of Hematology, Seoul St. Mary's Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Catholic Research Network for Multiple Myeloma, Seoul, Republic of Korea. Electronic address: sspark@catholic.ac.kr.
S JungDepartment of Pharmacology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Division of Data Science, PIPET, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
C H LeeDepartment of Pharmacology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Division of Data Science, PIPET, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
S HanDepartment of Pharmacology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Division of Data Science, PIPET, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea. Electronic address: waystolove@catholic.ac.kr.
C-K MinDepartment of Hematology, Seoul St. Mary's Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Catholic Research Network for Multiple Myeloma, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis nationwide real-world data cohort study developed a risk-scoring model to predict the progression of monoclonal gammopathy of undetermined significance (MGUS) to symptomatic multiple myeloma (MM) using prior disease conditions. MATERIALS AND

methodsThe Health Insurance Review and Assessment Service database, which covers nearly the entire Korean population, was utilized in this study. Out of 5361 MGUS patients, 345 (6.4%) were diagnosed with MM, with 253 (73.3%) of them progressing to symptomatic MM.

resultsWe identified female sex, chronic pulmonary disease, peptic ulcer disease, diabetes, and non-malignant hematologic disorder as significant risk factors and integrated these into the risk-scoring model. MGUS patients can be stratified into low-, intermediate-, and high-risk groups for progression to symptomatic MM using this model. The high-risk group showed a hazard ratio (HR) of 2.53 [95% confidence interval (CI) 1.70-3.75] compared with the low-risk group, and the intermediate-risk group showed an HR of 1.38 (95% CI 1.02-1.86) compared with the low-risk group.

conclusionThis scoring model will help in the early detection of MGUS patients at high risk for symptomatic MM and allow for a more efficient allocation of health care resources to those patients who require intensive monitoring.

Indexed as

Monoclonal Gammopathy of Undetermined SignificanceMultiple MyelomaAdultAgedCohort StudiesDisease ProgressionFemaleHumansMaleMiddle AgedRepublic of KoreaRisk AssessmentRisk FactorsMGUSmultiple myelomarisk scoring

Identifiers

PMID40644760
PMCPMC12308365

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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 OpenQuestion graph.