Evidence map›Paper›PMID 33526859›Full record

ArticleLeukemia2021

Impact of measurable residual disease by decentralized flow cytometry: a PETHEMA real-world study in 1076 patients with acute myeloid leukemia.

Bruno Paiva, María-Belen Vidriales, Amparo Sempere, Fabián Tarín, Enrique Colado, Celina Benavente, María-Teresa Cedena, Joaquín Sánchez, Teresa Caballero-Velazquez, Lourdes Cordón and 28 more

Abstract read
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In one paragraph

Article in Leukemia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Measurable Residual Disease.Methods in molecular biology (Clifton, N.J.) · 2027
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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

38 authors at 20 institutions in 4 countries.

Bruno Paiva *Clínica Universidad de Navarra, Centro de Investigación Médica Aplicada (CIMA), IDISNA, CIBER-ONC number CB16/12/00369, Pamplona, Spain.ORCID http://orcid.org/0000-0003-1977-3815
María-Belen Vidriales *Department of Hematology, University Hospital of Salamanca (HUS/IBSAL), CIBERONC (CB16/12/002333) and Center for Cancer Research-IBMCC (USAL-CSIC), Salamanca, Spain.ORCID http://orcid.org/0000-0001-5049-3673
Amparo Sempere *Hospital Universitario y Politécnico La Fe, CIBER-ONC number CB16/12/00284, Valencia, Spain.
Fabián TarínHospital General Universitario de Alicante, Alicante, Spain.
Enrique ColadoHospital Universitario Central de Asturias, Instituto de Investigación Sanitaria y Universitario Oncológico del Principado de Asturias (ISPA / IUOPA), Oviedo, Spain.
Celina BenaventeHospital Clínico San Carlos, Madrid, Spain.
María-Teresa CedenaHospital Universitario 12 de Octubre, Madrid, Spain.
Joaquín SánchezHospital Reina Sofía, Córdoba, Spain.
Teresa Caballero-VelazquezHopsital Universitario Virgen del Rocío, Instituto de Biomedicina (IBIS / CSIC / CIBERONC), Universidad de Sevilla, Sevilla, Spain.
Lourdes CordónHospital Universitario y Politécnico La Fe, CIBER-ONC number CB16/12/00284, Valencia, Spain.ORCID http://orcid.org/0000-0002-8808-3423
Juan-Jose GarcesClínica Universidad de Navarra, Centro de Investigación Médica Aplicada (CIMA), IDISNA, CIBER-ONC number CB16/12/00369, Pamplona, Spain.ORCID http://orcid.org/0000-0001-9235-4671
Catia SimoesClínica Universidad de Navarra, Centro de Investigación Médica Aplicada (CIMA), IDISNA, CIBER-ONC number CB16/12/00369, Pamplona, Spain.
David Martínez-CuadrónHospital Universitario y Politécnico La Fe, CIBER-ONC number CB16/12/00284, Valencia, Spain.ORCID http://orcid.org/0000-0001-7540-4091
Teresa BernalHospital Universitario Central de Asturias, Instituto de Investigación Sanitaria y Universitario Oncológico del Principado de Asturias (ISPA / IUOPA), Oviedo, Spain.ORCID http://orcid.org/0000-0002-2338-513X
Carmen BotellaHospital General Universitario de Alicante, Alicante, Spain.
Sofia GrilleHospital de Clinicas. Montevideo, Uruguay, Spain.
Josefina SerranoHospital Reina Sofía, Córdoba, Spain.
Carlos Rodríguez-MedinaHospital Universitario de Gran Canaria Doctor Negrin, Las Palmas, Spain.
Lorenzo AlgarraHospital General de Albacete, Albacete, Spain.
Juan-Manuel Alonso-DomínguezHospital Universitario Fundación Jiménez Díaz, Madrid, Spain.ORCID http://orcid.org/0000-0001-6233-5912
María-Luz AmigoHospital Morales Messeguer, Murcia, Spain.ORCID http://orcid.org/0000-0002-3356-9290
Manuel BarriosHospital Regional Universitario de Málaga, Malaga, Spain.
Raimundo García-BoyeroHospital General Universitario de Castellón, Castellón de la Plana, Spain.
Mercedes ColoradoHospital Universitario Marqués de Valdecilla, Santander, Spain.
Jaime Pérez-OteyzaHospital HM Madrid, Madrid, Spain.
Manuel Pérez-EncinasHospital Clinico de Santiago de Compostela, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0001-9943-4404
Lisette Costilla-BarrigaHospital Miguel Servet, Zaragoza, Spain.
María-José SayasHospital Universitario Dr. Peset, Valencia, Spain.
Olga PérezHospital Universitario Virgen Macarena, Sevilla, Spain.
Marcos González-DíazDepartment of Hematology, University Hospital of Salamanca (HUS/IBSAL), CIBERONC (CB16/12/002333) and Center for Cancer Research-IBMCC (USAL-CSIC), Salamanca, Spain.
José A Pérez-SimónHopsital Universitario Virgen del Rocío, Instituto de Biomedicina (IBIS / CSIC / CIBERONC), Universidad de Sevilla, Sevilla, Spain.
Joaquín Martínez-LópezHospital Universitario 12 de Octubre, Madrid, Spain.ORCID http://orcid.org/0000-0001-7908-0063
Claudia SossaClinica FOSCAL, Santander, Colombia.
Alberto OrfaoCancer Research Center (IBMCC-CSIC/USAL-IBSAL); Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca, Salamanca, Spain.ORCID http://orcid.org/0000-0002-0007-7230
Jesús F San MiguelClínica Universidad de Navarra, Centro de Investigación Médica Aplicada (CIMA), IDISNA, CIBER-ONC number CB16/12/00369, Pamplona, Spain.
Miguel-Ángel SanzHospital Universitario y Politécnico La Fe, CIBER-ONC number CB16/12/00284, Valencia, Spain.ORCID http://orcid.org/0000-0003-1489-1177
Pau MontesinosHospital Universitario y Politécnico La Fe, CIBER-ONC number CB16/12/00284, Valencia, Spain. montesinos_pau@gva.es.ORCID http://orcid.org/0000-0002-3275-5593
PETHEMA (Programa para el Estudio de la Terapéutica en Hemopatías Malignas) cooperative study group
Hospital Universitari i Politècnic La Fe · ESClinica Universidad de Navarra · ESCentro de Investigación Biomédica en Red de Cáncer · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital Universitario 12 De Octubre · ESHospital Universitario Reina Sofía · ESInstituto de Investigación Biomédica de Salamanca · ESInstituto de Investigación Sanitaria del Principado de Asturias · ESComplejo Hospitalario Universitario de Santiago · ESFoscal Hospital · COHospital Clínico San Carlos · ESHospital de Clínicas · UYHospital General Universitari de Castelló · ESHospital General Universitario de Albacete · ESHospital General Universitario Morales Meseguer · ESHospital Regional Universitario de Málaga · ESHospital Universitario de Gran Canaria Doctor Negrín · ESHospital Universitario Doctor Peset · ESHospital Universitario Fundación Jiménez Díaz · ESHospital Universitario Miguel Servet · ES

Funding

Cancer Research UK
6 · The paper itself

Abstract

The role of decentralized assessment of measurable residual disease (MRD) for risk stratification in acute myeloid leukemia (AML) remains largely unknown, and so it does which methodological aspects are critical to empower the evaluation of MRD with prognostic significance, particularly if using multiparameter flow cytometry (MFC). We analyzed 1076 AML patients in first remission after induction chemotherapy, in whom MRD was evaluated by MFC in local laboratories of 60 Hospitals participating in the PETHEMA registry. We also conducted a survey on technical aspects of MRD testing to determine the impact of methodological heterogeneity in the prognostic value of MFC. Our results confirmed the recommended cutoff of 0.1% to discriminate patients with significantly different cumulative-incidence of relapse (-CIR- HR:0.71, P < 0.001) and overall survival (HR: 0.73, P = 0.001), but uncovered the limited prognostic value of MFC based MRD in multivariate and recursive partitioning models including other clinical, genetic and treatment related factors. Virtually all aspects related with methodological, interpretation, and reporting of MFC based MRD testing impacted in its ability to discriminate patients with different CIR. Thus, this study demonstrated that "real-world" assessment of MRD using MFC is prognostic in patients at first remission, and urges greater standardization for improved risk-stratification toward clinical decisions in AML.

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyDisease ProgressionFemaleFlow CytometryFollow-Up StudiesHematopoietic Stem Cell TransplantationHumansInduction ChemotherapyLeukemia, Myeloid, AcuteMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm, ResidualPrognosis

Identifiers

PMID33526859
OpenAlexW3128365485

What OpenQuestion holds

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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.