Evidence map›Paper›PMID 41664570›Full record

ArticleJournal of Korean medical science2026

Complementary Roles of Next-Generation Flow and Next-Generation Sequencing for Measurable Residual Disease Assessment in Multiple Myeloma.

Min-Seung Park, Dae Jin Lim, Hee-Jin Kim, Duck Cho, Sang Eun Yoon, Seok Jin Kim, Kihyun Kim, Hyun-Young Kim

Abstract read
In one paragraph

Article in Journal of Korean medical science, 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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0citing papers in PubMed
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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

8 authors.

Min-Seung Park *Department of Laboratory Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-4482-3098
Dae Jin Lim *Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-3079-5716
Hee-Jin KimDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-3741-4613
Duck ChoDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-6861-3282
Sang Eun YoonDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0379-5297
Seok Jin KimDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-2776-4401
Kihyun KimDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. kihyunkimk@gmail.com.ORCID https://orcid.org/0000-0002-5878-8895
Hyun-Young KimDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. hysck.kim@gmail.com.ORCID https://orcid.org/0000-0003-0553-7096

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHighly sensitive measurable residual disease (MRD) assays play a crucial role in predicting prognosis and guiding further treatment in multiple myeloma (MM). This study aimed to compare the diagnostic performance and clinical utility of next-generation flow (NGF)- and next-generation sequencing (NGS)-based MRD assays in patients with MM.

methodsWe evaluated 55 bone marrow (BM) aspirate samples from 41 MM patients for MRD. NGF-MRD was performed on fresh BM specimens in accordance with EuroFlow standard operating procedures, whereas NGS-MRD was conducted on archived BM DNA using the LymphoTrack

resultsThe MRD detection rates were 43.6% (24/55) for NGF-MRD and 29.1% (16/55) for NGS-MRD with 67.3% (37/55) concordance rate between two MRD assays, and correlation coefficient (

conclusionBoth NGF-MRD and NGS-MRD play critical and complementary roles in monitoring MRD in MM. Notably, even isolated MRD positivity detected by either method was associated with disease progression in certain cases, underscoring the importance of both MRD assays.

Indexed as

High-Throughput Nucleotide SequencingMultiple MyelomaNeoplasm, ResidualAdultAgedBone MarrowFemaleHumansMaleMiddle AgedPrognosisProgression-Free SurvivalMeasurable Residual DiseaseMultiple MyelomaNext-Generation FlowNext-Generation SequencingProgression-Free Survival

Identifiers

PMID41664570
PMCPMC12890463

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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.