Evidence map›Paper›PMID 33916787›Full record

ArticleCancers2021

B-Cell Regeneration Profile and Minimal Residual Disease Status in Bone Marrow of Treated Multiple Myeloma Patients.

Robéria Mendonça de Pontes, Juan Flores-Montero, Luzalba Sanoja-Flores, Noemi Puig, Roberto J Pessoa de Magalhães, Alba Corral-Mateos, Anna Beatriz Salgado, Omar García-Sánchez, José Pérez-Morán, Maria-Victoria Mateos and 15 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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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

25 authors at 11 institutions in 4 countries.

Robéria Mendonça de PontesInternal Medicine Postgraduate Program, Faculty of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-617, Brazil.ORCID 0000-0003-3608-8254
Juan Flores-MonteroTranslational and Clinical Research Program, Cancer Research Center (IBMCC, USAL-CSIC), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca, Institute of Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain.ORCID 0000-0002-1119-4387
Luzalba Sanoja-FloresCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.ORCID 0000-0002-9275-7793
Noemi PuigCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.
Roberto J Pessoa de MagalhãesDepartment of Internal Medicine, University Hospital Clementino Fraga Filho, Faculty of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-617, Brazil.
Alba Corral-MateosTranslational and Clinical Research Program, Cancer Research Center (IBMCC, USAL-CSIC), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca, Institute of Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain.
Anna Beatriz SalgadoInternal Medicine Postgraduate Program, Faculty of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-617, Brazil.
Omar García-SánchezCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.
José Pérez-MoránCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.
Maria-Victoria MateosCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.ORCID 0000-0003-2390-1218
Leire BurgosCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.
Bruno PaivaCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.
Jeroen Te MarveldeDepartment of Immunology, Erasmus MC, (EMC) University Medical Center Rotterdam, 3015 GA Rotterdam, The Netherlands.
Vincent H J van der VeldenDepartment of Immunology, Erasmus MC, (EMC) University Medical Center Rotterdam, 3015 GA Rotterdam, The Netherlands.
Carlos AguilarDepartment of Hematology, Hospital General de Santa Bárbara, 42005 Soria, Spain.ORCID 0000-0002-5225-6687
Abelardo BárezDepartment of Hematology, Complejo Asistencial de Ávila, 05071 Ávila, Spain.ORCID 0000-0001-8982-6105
Aranzazú García-MateoDepartment of Hematology, Complejo Asistencial de Segovia, 40002 Segovia, Spain.
Jorge LabradorDepartment of Hematology and Research Unit, Hospital Universitario de Burgos, 09006 Burgos, Spain.ORCID 0000-0002-3696-0287
Pilar LeozCentro de Investigación Biomédica en Red de Cáncer (CIBERONC) (CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489 and CB16/12/00480), Instituto Carlos III, 28029 Madrid, Spain.
Carmen Aguilera-SanzDepartment of Hematology, Hospital El Bierzo, 24404 Ponferrada, Spain.
Brian DurieCedars-Sinai Samuel Oschin Cancer Center, Los Angeles, CA 90048, USA.
Jacques J M van DongenDepartment of Immunology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Angelo MaiolinoInternal Medicine Postgraduate Program, Faculty of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-617, Brazil.
Elaine Sobral da CostaInternal Medicine Postgraduate Program, Faculty of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro 21941-617, Brazil.
Alberto OrfaoTranslational and Clinical Research Program, Cancer Research Center (IBMCC, USAL-CSIC), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca, Institute of Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain.ORCID 0000-0002-0007-7230
Universidad de Salamanca · ESUniversidade Federal do Rio de Janeiro · BRErasmus MC · NLNavarre Institute of Health Research · ESCatholic University of Ávila · ESCedars-Sinai Medical Center · USConsejo Superior de Investigaciones Científicas · ESHospital El Bierzo · ESHospital General De Segovia · ESHospital Universitario de Burgos · ESLeiden University Medical Center · NL

Funding

Centro de Investigación Biomédica en Red de Cáncer CB16/12/00400, CB16/12/00233, CB16/12/00369, CB16/12/00489, CB16/12/00480Conselho Nacional de Desenvolvimento Científico e Tecnológico of Brazil (CNPQ) 400194/2014-7Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES/DGPU) 000281/2016-06Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES-PROEX) 641/2018Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro of Brazil (FAPERJ) E26/110.105/2014, E26/102.191/2013 and E01/200/537/2018
6 · The paper itself

Abstract

B-cell regeneration during therapy has been considered as a strong prognostic factor in multiple myeloma (MM). However, the effects of therapy and hemodilution in bone marrow (BM) B-cell recovery have not been systematically evaluated during follow-up. MM (n = 177) and adult (≥50y) healthy donor (HD; n = 14) BM samples were studied by next-generation flow (NGF) to simultaneously assess measurable residual disease (MRD) and residual normal B-cell populations. BM hemodilution was detected in 41 out of 177 (23%) patient samples, leading to lower total B-cell, B-cell precursor (BCP) and normal plasma cell (nPC) counts. Among MM BM, decreased percentages (vs. HD) of BCP, transitional/naïve B-cell (TBC/NBC) and nPC populations were observed at diagnosis. BM BCP increased after induction therapy, whereas TBC/NBC counts remained abnormally low. At day+100 postautologous stem cell transplantation, a greater increase in BCP with recovered TBC/NBC cell numbers but persistently low memory B-cell and nPC counts were found. At the end of therapy, complete response (CR) BM samples showed higher CD19

Indexed as

B-cell regenerationhemodilutionimmunophenotypingmeasurable residual diseasemultiple myeloma

Identifiers

PMID33916787
PMCPMC8038337
OpenAlexW3145332580

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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.