Evidence map›Paper›PMID 41649556›Full record

ArticleAnnals of hematology2026

Real-world outcomes of SLiM-only multiple myeloma: Korean Multicenter Retrospective analysis (KMM2401 study).

Jun Ho Yi, Dok Hyun Yoon, Sung-Soo Park, Chang-Ki Min, Ji Hyun Lee, Sung-Hoon Jung, Youngil Koh, Hyun Jung Lee, Jae-Cheol Jo, Kihyun Kim

Abstract readMulticenter Study
In one paragraph

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

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jun Ho YiDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Dok Hyun YoonDepartment of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Sung-Soo ParkDepartment of Hematology, Catholic Hematology Hospital, Seoul St. Mary's Hospital, Catholic University, Seoul, Korea.
Chang-Ki MinDepartment of Hematology, Catholic Hematology Hospital, Seoul St. Mary's Hospital, Catholic University, Seoul, Korea.
Ji Hyun LeeDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Sung-Hoon JungDepartment of Hematology-Oncology, Chonnam National University Hwasun Hospital and Chonnam National University Medical School, Hwasun-Gun, Jeollanam-Do, Korea.
Youngil KohDepartment of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Hyun Jung LeeDivision of Hematology and Medical Oncology, Department of Internal Medicine, Kyung Hee University College of Medicine, Kyung Hee University Hospital, Seoul, Korea.
Jae-Cheol JoDepartment of Hematology and Oncology, Ulsan University Hospital, University of Ulsan College of Medicine, Dong-Gu, Ulsan, 44033, Korea.
Kihyun KimDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. kihyunk@skku.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the 2014 update, SLiM biomarkers were included into the "myeloma defining events" as these markers were shown to be significantly associated with early progression to active multiple myeloma (MM). However, several subsequent studies have reported more favorable outcomes. To further clarify the clinical implications, we conducted a retrospective analysis. Patients diagnosed with MM based solely on SLiM biomarkers (SLiM-only MM) 8-17were included. Patients were analyzed according to whether they underwent active observation (group 1) or immediate treatment (group 2). From 2011 to 2023, 72 cases were collected from 8 tertiary institutes in Korea. The median age was 65, and 40 (56%) were male. In terms of the SLiM criteria, 27 patients had bone marrow plasma cell(BMPC) ≥ 60%, 31 patients had serum free light chain ratio (FLCr) ≥ 100, and 35 patients had > 1 focal lesion on MRI. Thirty-five patients were included in group 1, and the median time to progression to MM was 75.8 months. Regardless of the fulfilled SLiM criteria, patients exhibited lower 2-year risk of progression to MM compared with previous studies. Patients with > 1 focal lesion on MRI showed significantly lower 2-year risk of progression than those with BMPC ≥ 60% or FLCr ≥ 100 (p = 0.014). In group 2, the estimated median PFS was 56.8 months. Patients with SLiM-only MM exhibited an extended TTP without treatment compared to prior studies, particularly those with > 1 focal lesions on MRI. In addition, the first-line treatment resulted in favorable outcomes, which may support the benefit of earlier initiation of treatment.

Indexed as

Biomarkers, TumorMultiple MyelomaAgedDisease ProgressionFemaleHumansImmunoglobulin Light ChainsMaleMiddle AgedPlasma CellsRepublic of KoreaRetrospective StudiesTreatment OutcomeBiomarkers, TumorImmunoglobulin Light ChainsDiagnosisMultiple myelomaSLiM criteriaTreatment

Identifiers

PMID41649556
PMCPMC12881067

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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.