Evidence map›Paper›PMID 38072838›Full record

ArticleBlood cancer journal2023

Immunophenotypic assessment of clonal plasma cells and B-cells in bone marrow and blood in the diagnostic classification of early stage monoclonal gammopathies: an iSTOPMM study.

Oihane Pérez-Escurza, Juan Flores-Montero, Jón Þórir Óskarsson, Luzalba Sanoja-Flores, Julio Del Pozo, Quentin Lecrevisse, Silvia Martín, Elín Ruth Reed, Guðlaug Katrín Hákonardóttir, Stephen Harding and 6 more

Abstract read
In one paragraph

Article in Blood cancer journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

16 authors.

Oihane Pérez-EscurzaTranslational and Clinical Research Program, Cancer Research Center (IBMCC, CSIC-University of Salamanca); Cytometry Service, NUCLEUS; Department of Medicine, University of Salamanca (Universidad de Salamanca), Salamanca, Spain.ORCID 0000-0002-6966-4337
Juan Flores-MonteroTranslational and Clinical Research Program, Cancer Research Center (IBMCC, CSIC-University of Salamanca); Cytometry Service, NUCLEUS; Department of Medicine, University of Salamanca (Universidad de Salamanca), Salamanca, Spain.ORCID 0000-0002-1119-4387
Jón Þórir ÓskarssonFaculty of Medicine, University of Iceland, Reykjavík, Iceland.ORCID 0000-0002-9201-1166
Luzalba Sanoja-FloresBiomedical Research Networking Centre Consortium of Oncology (CIBERONC), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0002-9275-7793
Julio Del PozoTranslational and Clinical Research Program, Cancer Research Center (IBMCC, CSIC-University of Salamanca); Cytometry Service, NUCLEUS; Department of Medicine, University of Salamanca (Universidad de Salamanca), Salamanca, Spain.
Quentin LecrevisseTranslational and Clinical Research Program, Cancer Research Center (IBMCC, CSIC-University of Salamanca); Cytometry Service, NUCLEUS; Department of Medicine, University of Salamanca (Universidad de Salamanca), Salamanca, Spain.ORCID 0000-0001-8715-5846
Silvia MartínTranslational and Clinical Research Program, Cancer Research Center (IBMCC, CSIC-University of Salamanca); Cytometry Service, NUCLEUS; Department of Medicine, University of Salamanca (Universidad de Salamanca), Salamanca, Spain.
Elín Ruth ReedFaculty of Medicine, University of Iceland, Reykjavík, Iceland.
Guðlaug Katrín HákonardóttirFaculty of Medicine, University of Iceland, Reykjavík, Iceland.
Stephen HardingThe Binding Site Group, Birmingham, UK.
Sigrún ÞorsteinsdóttirFaculty of Medicine, University of Iceland, Reykjavík, Iceland.ORCID 0000-0001-5017-3530
Sæmundur RögnvaldssonFaculty of Medicine, University of Iceland, Reykjavík, Iceland.
Thorvardur Jon LoveFaculty of Medicine, University of Iceland, Reykjavík, Iceland.
Brian DurieDepartment of Hematology and Oncology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Sigurður Yngvi KristinssonFaculty of Medicine, University of Iceland, Reykjavík, Iceland.ORCID 0000-0002-4964-7476
Alberto OrfaoTranslational and Clinical Research Program, Cancer Research Center (IBMCC, CSIC-University of Salamanca); Cytometry Service, NUCLEUS; Department of Medicine, University of Salamanca (Universidad de Salamanca), Salamanca, Spain. orfao@usal.es.ORCID 0000-0002-0007-7230

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 716677, 101045549Icelandic Centre for Research (Rannsóknamiðstöð Íslands) 173857, 217897-051 and 228521-051
6 · The paper itself

Abstract

Monoclonal gammopathy of undetermined significance (MGUS) is the earliest discernible stage of multiple myeloma (MM) and Waldenström's macroglobulinemia (WM). Early diagnosis of MG may be compromised by the low-level infiltration, undetectable to low-sensitive methodologies. Here, we investigated the prevalence and immunophenotypic profile of clonal (c) plasma cells (PC) and/or cB-lymphocytes in bone marrow (BM) and blood of subjects with a serum M-component from the iSTOPMM program, using high-sensitive next-generation flow cytometry (NGF), and its utility in the diagnostic classification of early-stage MG. We studied 164 paired BM and blood samples from 82 subjects, focusing the analysis on: 55 MGUS, 12 smoldering MM (SMM) and 8 smoldering WM (SWM). cPC were detected in 84% of the BM samples and cB-lymphocytes in 45%, coexisting in 39% of cases. In 29% of patients, the phenotypic features of cPC and/or cB-lymphocytes allowed a more accurate disease classification, including: 19/55 (35%) MGUS, 1/12 (8%) SMM and 2/8 (25%) SWM. Blood samples were informative in 49% of the BM-positive cases. We demonstrated the utility of NGF for a more accurate diagnostic classification of early-stage MG.

Indexed as

Monoclonal Gammopathy of Undetermined SignificanceMultiple MyelomaParaproteinemiasSmoldering Multiple MyelomaWaldenstrom MacroglobulinemiaB-LymphocytesBone MarrowHumansPlasma Cells

Identifiers

PMID38072838
PMCPMC10711003

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