Evidence map›Paper›PMID 38493239›Full record

ArticleLeukemia2024

Beyond the marrow: insights from comprehensive next-generation sequencing of extramedullary multiple myeloma tumors.

T Jelinek, D Zihala, T Sevcikova, A Anilkumar Sithara, V Kapustova, H Sahinbegovic, O Venglar, L Muronova, L Broskevicova, S Nenarokov and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
16.4field-weighted citation impact, top 1% of its field
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

39 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
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  10. Article
  11. Article
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  13. Observational
  14. Extramedullary Disease-Achilles Heel in Myeloma?American journal of hematology · 2026
    Review
  15. Synthesis, preclinical evaluation and clinical application of a novel heterodimeric tracerEuropean journal of nuclear medicine and molecular imaging · 2026
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

22 authors at 3 institutions in 2 countries.

T Jelinek *Department of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.ORCID 0000-0002-5467-9253
D Zihala *Department of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
T Sevcikova *Department of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
A Anilkumar SitharaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.ORCID 0000-0003-2540-6966
V KapustovaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
H SahinbegovicDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
O VenglarDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
L MuronovaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
L BroskevicovaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
S NenarokovDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
D BilekDepartment of Biology and Ecology, Faculty of Science, University of Ostrava, Ostrava, Czech Republic.
T PopkovaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.ORCID 0000-0001-5885-4218
H PlonkovaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
J VranaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
V ZidlikDepartment of Pathology, University Hospital Ostrava, Ostrava, Czech Republic.
P HurnikDepartment of Pathology, University Hospital Ostrava, Ostrava, Czech Republic.
M HavelDepartment of Nuclear Medicine, University Hospital Ostrava, Ostrava, Czech Republic.ORCID 0000-0001-7444-5422
M HrdinkaDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.ORCID 0000-0002-2981-2825
Z ChyraDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
G StracquadanioSchool of Biological Sciences, The University of Edinburgh, Edinburgh, EH9 3BF, UK.ORCID 0000-0001-9819-3645
M SimicekDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.ORCID 0000-0003-2388-2723
R HajekDepartment of Hematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic. roman.hajek@fno.cz.ORCID 0000-0001-6955-6267
University of Ostrava · CZUniversity Hospital Ostrava · CZUniversity of Edinburgh · GB

Funding

Agentura Pro Zdravotnický Výzkum České Republiky (Czech Health Research Council) NU23-03-00374EC | European Regional Development Fund (Europski Fond za Regionalni Razvoj) CZ.02.1.01/0.0/0.0/16_019/0000868EC | European Regional Development Fund (Europski Fond za Regionalni Razvoj) No. CZ.02.1.01/0.0/0.0/16_019/0000868Ministerstvo Zdravotnictví Ceské Republiky (Ministry of Health of the Czech Republic) MH CZ- DRO-FNOs/2020
6 · The paper itself

Abstract

Extramedullary multiple myeloma (EMM) is an aggressive form of multiple myeloma (MM). This study represents the most comprehensive next-generation sequencing analysis of EMM tumors (N = 14) to date, uncovering key molecular features and describing the tumor microenvironment. We observed the co-occurrence of 1q21 gain/amplification and MAPK pathway mutations in 79% of EMM samples, suggesting that these are crucial mutational events in EMM development. We also demonstrated that patients with mutated KRAS and 1q21 gain/amplification at the time of diagnosis have a significantly higher risk of EMM development (HR = 2.4, p = 0.011) using data from a large CoMMpass dataset. We identified downregulation of CXCR4 and enhanced cell proliferation, along with reduced expression of therapeutic targets (CD38, SLAMF7, GPRC5D, FCRH5), potentially explaining diminished efficacy of immunotherapy. Conversely, we identified significantly upregulated EZH2 and CD70 as potential future therapeutic options. For the first time, we report on the tumor microenvironment of EMM, revealing CD8+ T cells and NK cells as predominant immune effector cells using single-cell sequencing. Finally, this is the first longitudinal study in EMM revealing the molecular changes from the time of diagnosis to EMM relapse.

Indexed as

High-Throughput Nucleotide SequencingMultiple MyelomaTumor MicroenvironmentAgedBiomarkers, TumorBone MarrowFemaleHumansMaleMiddle AgedMutationPrognosisBiomarkers, Tumor

Identifiers

PMID38493239
PMCPMC11147761
OpenAlexW4392881499

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.