Evidence map›Paper›PMID 32475991›Full record

ArticleLeukemia2020

Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma.

Juan-José Garcés, Gabriel Bretones, Leire Burgos, Rafael Valdes-Mas, Noemi Puig, Maria-Teresa Cedena, Diego Alignani, Idoia Rodriguez, Diana Álvarez Puente, Miguel-García Álvarez and 24 more

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In one paragraph

Article in Leukemia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 44 citations in OpenAlex.

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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

34 authors at 9 institutions in 2 countries.

Juan-José Garcés *Clinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.ORCID http://orcid.org/0000-0001-9235-4671
Gabriel Bretones *Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Universidad de Oviedo, Oviedo, Spain.
Leire Burgos *Clinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.
Rafael Valdes-MasDepartamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Universidad de Oviedo, Oviedo, Spain.
Noemi PuigHospital Universitario de Salamanca, Instituto de Investigacion Biomedica de Salamanca (IBSAL), Centro de Investigación del Cancer (IBMCC-USAL, CSIC), Salamanca, Spain.
Maria-Teresa CedenaHospital Universitario 12 de Octubre, Madrid, Spain.
Diego AlignaniClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.
Idoia RodriguezClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.
Diana Álvarez PuenteDepartamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Universidad de Oviedo, Oviedo, Spain.
Miguel-García ÁlvarezDepartamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Universidad de Oviedo, Oviedo, Spain.
Ibai GoicoecheaClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.ORCID http://orcid.org/0000-0002-5329-2225
Sara RodriguezClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.
Maria-Jose CalasanzClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.
Xabier AgirreClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.ORCID http://orcid.org/0000-0002-6558-9560
Juan Flores-MonteroCancer Research Center (IBMCC-CSIC/USAL-IBSAL), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca (USAL), Salamanca, Spain.ORCID http://orcid.org/0000-0002-1119-4387
Luzalba Sanoja-FloresCancer Research Center (IBMCC-CSIC/USAL-IBSAL), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca (USAL), Salamanca, Spain.ORCID http://orcid.org/0000-0002-9275-7793
Paula Rodriguez-OteroClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.
Rafael RiosHospital Universitario Virgen de las Nieves, Granada, Spain.
Joaquin Martinez-LopezHospital Universitario 12 de Octubre, Madrid, Spain.
Pamela MillacoyComplejo Hospitalario de Navarra, Pamplona, Spain.
Luis PalomeraHospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.
Rafael Del OrbeBiocruces Health Research Institute, Barakaldo, Spain.ORCID http://orcid.org/0000-0002-1240-1958
Albert Pérez-MontañaHospital Universitario Son Espases, Palma, Spain.
Halima El OmriNational Center for Cancer Care and Research, Hamad Medical Corporation, Doha, Qatar.
Felipe ProsperClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.ORCID http://orcid.org/0000-0001-6115-8790
Maria-Victoria MateosHospital Universitario de Salamanca, Instituto de Investigacion Biomedica de Salamanca (IBSAL), Centro de Investigación del Cancer (IBMCC-USAL, CSIC), Salamanca, Spain.ORCID http://orcid.org/0000-0003-2390-1218
Laura RosiñolHospital Clínic, IDIBAPS, Barcelona, Spain.
Joan BladeHospital Clínic, IDIBAPS, Barcelona, Spain.
Juan-Jose LahuertaHospital Universitario 12 de Octubre, Madrid, Spain.
Alberto OrfaoCancer Research Center (IBMCC-CSIC/USAL-IBSAL), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca (USAL), Salamanca, Spain.
Carlos Lopez-OtinDepartamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Universidad de Oviedo, Oviedo, Spain.ORCID http://orcid.org/0000-0001-6964-1904
Jesus F San MiguelClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain.
Bruno PaivaClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), Navarra, Spain. bpaiva@unav.es.ORCID http://orcid.org/0000-0003-1977-3815
GEM/PETHEMA (Grupo Español de Mieloma/Programa para el Estudio de la Terapéutica en Hemopatías Malignas) cooperative study group
Navarre Institute of Health Research · ESUniversidad de Oviedo · ESHospital Universitario 12 De Octubre · ESUniversidad de Salamanca · ESBioCruces Health research Institute · ESComplejo Hospitalario de Navarra · ESHospital Clínic de Barcelona · ESClinica Universidad de Navarra · ESNational Center for Cancer Care and Research · QA

Funding

American Association for Cancer Research (American Association for Cancer Research, Inc.) 15-40-38-PAIVInternational Myeloma Foundation (IMF) Black Swan Research InitiativeLeukemia Research Foundation (LRF) NAMultiple Myeloma Research Foundation (Multiple Myeloma Research Foundation, Inc.) 2019 Research Fellowship AwardQatar National Research Fund (QNRF) 7-916-3-237
6 · The paper itself

Abstract

Multiple myeloma (MM) patients undergo repetitive bone marrow (BM) aspirates for genetic characterization. Circulating tumor cells (CTCs) are detectable in peripheral blood (PB) of virtually all MM cases and are prognostic, but their applicability for noninvasive screening has been poorly investigated. Here, we used next-generation flow (NGF) cytometry to isolate matched CTCs and BM tumor cells from 53 patients and compared their genetic profile. In eight cases, tumor cells from extramedullary (EM) plasmacytomas were also sorted and whole-exome sequencing was performed in the three spatially distributed tumor samples. CTCs were detectable by NGF in the PB of all patients with MM. Based on the cancer cell fraction of clonal and subclonal mutations, we found that ~22% of CTCs egressed from a BM (or EM) site distant from the matched BM aspirate. Concordance between BM tumor cells and CTCs was high for chromosome arm-level copy number alterations (≥95%) though not for translocations (39%). All high-risk genetic abnormalities except one t(4;14) were detected in CTCs whenever present in BM tumor cells. Noteworthy, ≥82% mutations present in BM and EM clones were detectable in CTCs. Altogether, these results support CTCs for noninvasive risk-stratification of MM patients based on their numbers and genetic profile.

Indexed as

Biomarkers, TumorComputational BiologyDNA Copy Number VariationsDNA Mutational AnalysisFemaleGenetic HeterogeneityHumansImmunophenotypingLiquid BiopsyMaleMultiple MyelomaMutationNeoplasm StagingNeoplastic Cells, CirculatingPrognosisRecurrenceBiomarkers, Tumor

Identifiers

PMID32475991
OpenAlexW3031012053

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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.