Evidence map›Paper›PMID 35821023›Full record

ArticleBlood cancer journal2022

A scoring system for AML patients aged 70 years or older, eligible for intensive chemotherapy: a study based on a large European data set using the DATAML, SAL, and PETHEMA registries.

Emilie Bérard, Christoph Röllig, Sarah Bertoli, Arnaud Pigneux, Suzanne Tavitian, Michael Kramer, Hubert Serve, Martin Bornhäuser, Uwe Platzbecker, Carsten Müller-Tidow and 14 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2022. 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
1.1field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
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  4. 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

24 authors at 17 institutions in 4 countries.

Emilie BérardCentre Hospitalier Universitaire de Toulouse, Service d'Epidémiologie, CERPOP, Inserm, Université Toulouse III Paul Sabatier, Toulouse, France.
Christoph Röllig *Medizinische Klinik und Poliklinik I, Universitätsklinikum TU Dresden, Dresden, Germany.
Sarah BertoliCentre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Université Toulouse III Paul Sabatier, Toulouse, France.ORCID 0000-0003-1084-2781
Arnaud PigneuxCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Université de Bordeaux, Institut National de la Santé et de la Recherche Médicale, U1035, 33000, Bordeaux, France.
Suzanne TavitianCentre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Université Toulouse III Paul Sabatier, Toulouse, France.
Michael KramerMedizinische Klinik und Poliklinik I, Universitätsklinikum TU Dresden, Dresden, Germany.
Hubert ServeMedizinische Klinik 2, Universitätsklinikum Frankfurt, Frankfurt/Main, Germany.
Martin BornhäuserMedizinische Klinik und Poliklinik I, Universitätsklinikum TU Dresden, Dresden, Germany.
Uwe PlatzbeckerKlinik und Poliklinik für Hämatologie, Zelltherapie und Hämostaseologie, Universitätsklinikum Leipzig, Leipzig, Germany.
Carsten Müller-TidowKlinik für Hämatologie, Onkologie und Rheumatologie, Universitätsklinikum Heidelberg, Heidelberg, Germany.
Claudia D BaldusKlinik für Innere Medizin II, Universitätsklinikum Schleswig-Holstein, Kiel, Germany.ORCID 0000-0002-0748-834X
David Martínez-CuadrónHospital Universitari i Politècnic La Fe, Valencia, Spain; Instituto de Investigación Sanitaria La Fe (IISLAFE), Valencia, Spain.ORCID 0000-0001-7540-4091
Josefina SerranoHospital Universitario Reina Sofía-IMIBIC, Córdoba, Spain.
Pilar Martínez-SánchezHospital Universitario 12 de Octubre, Madrid, Spain.
Eduardo Rodríguez ArbolíHospital Universitario Virgen del Rocío, Sevilla, Spain.ORCID 0000-0002-2237-6733
Cristina GilHospital General Universitario de Alicante, Alicante, Spain.
Juan BerguaHospital San Pedro Alcántara, Cáceres, Spain.
Teresa BernalHospital Universitario Central de Asturias, Asturias, Spain.
Adolfo de la Fuente BurgueraMD Anderson Cancer Center Madrid, Madrid, Spain.
Eric DelabesseCentre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Laboratoire d'Hématologie Biologique, Toulouse, France.ORCID 0000-0002-0928-0753
Audrey BidetCHU Bordeaux, Laboratoire d'Hématologie Biologique, F-33000, Bordeaux, France.ORCID 0000-0003-0992-8377
Pierre-Yves Dumas *CHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Université de Bordeaux, Institut National de la Santé et de la Recherche Médicale, U1035, 33000, Bordeaux, France.
Pau Montesinos *Hospital Universitari i Politècnic La Fe, Valencia, Spain; Instituto de Investigación Sanitaria La Fe (IISLAFE), Valencia, Spain.ORCID 0000-0002-3275-5593
Christian Récher *Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Université Toulouse III Paul Sabatier, Toulouse, France. recher.christian@iuct-oncopole.fr.ORCID 0000-0002-3332-4525
Université Toulouse III - Paul Sabatier · FRKlinik und Poliklinik für Psychotherapie und Psychosomatik · DEHospital Universitari i Politècnic La Fe · ESUniversité de Bordeaux · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Toulouse · FRGoethe University Frankfurt · DEHeidelberg University · DEHospital San Pedro de Alcántara · ESHospital Universitario 12 De Octubre · ESHospital Universitario Central de Asturias · ESHospital Universitario Virgen del Rocío · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESMD Anderson Cancer Center Madrid · ESUniversity Hospital Leipzig · DEUniversity Medical Center · USUniversity of Alicante · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In a context of therapeutic revolution in older adults with AML, it is becoming increasingly important to select patients for the various treatment options by taking account of short-term efficacy and toxicity as well as long-term survival. Here, the data from three European registries for 1,199 AML patients aged 70 years or older treated with intensive chemotherapy were used to develop a prognostic scoring system. The median follow-up was 50.8 months. In the training set of 636 patients, age, performance status, secondary AML, leukocytosis, and cytogenetics, as well as NPM1 mutations (without FLT3-ITD), were all significantly associated with overall survival, albeit not to the same degree. These factors were used to develop a score that predicts long-term overall survival. Three risk-groups were identified: a lower, intermediate and higher-risk score with predicted 5-year overall survival (OS) probabilities of ≥12% (n = 283, 51%; median OS = 18 months), 3-12% (n = 226, 41%; median OS = 9 months) and <3% (n = 47, 8%; median OS = 3 months), respectively. This scoring system was also significantly associated with complete remission, early death and relapse-free survival; performed similarly in the external validation cohort (n = 563) and showed a lower false-positive rate than previously published scores. The European Scoring System ≥70, easy for routine calculation, predicts long-term survival in older AML patients considered for intensive chemotherapy.

Indexed as

Leukemia, Myeloid, AcuteNuclear ProteinsAgedHumansMutationNeoplasm Recurrence, LocalNucleophosminPrognosisRegistriesNuclear ProteinsNucleophosmin

Identifiers

PMID35821023
PMCPMC9276717
OpenAlexW4285039745

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.