Evidence map›Paper›PMID 34615986›Full record

Trial reportLeukemia2022

Machine learning identifies the independent role of dysplasia in the prediction of response to chemotherapy in AML.

Matthieu Duchmann, Orianne Wagner-Ballon, Thomas Boyer, Meyling Cheok, Elise Fournier, Estelle Guerin, Laurène Fenwarth, Bouchra Badaoui, Nicolas Freynet, Emmanuel Benayoun and 15 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-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

8 citing papers in PubMed, 12 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 9 institutions in 1 country.

Matthieu DuchmannLaboratoire d'Hématologie, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France.
Orianne Wagner-BallonDépartement d'Hématologie et Immunologie biologiques, Hôpital Henri-Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, France.ORCID http://orcid.org/0000-0001-9071-6683
Thomas BoyerService d'Hématologie Biologique, CHU Lille, Lille, France.
Meyling CheokUMR9020 CNRS - UMR-S1277 INSERM, Lille, France.ORCID http://orcid.org/0000-0002-7820-8026
Elise FournierService d'Hématologie Biologique, CHU Lille, Lille, France.
Estelle GuerinService d'Hématologie biologique, Hôpital Dupuytren, Limoges, France.
Laurène FenwarthUniversité Lille, CNRS, INSERM, CHU Lille, IRCL, UMR9020 - UMR1277 - Canther - Cancer Heterogeneity, Plasticity and Resistance to Therapies, 59000, Lille, France.ORCID http://orcid.org/0000-0003-2808-4843
Bouchra BadaouiDépartement d'Hématologie et Immunologie biologiques, Hôpital Henri-Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, France.
Nicolas FreynetDépartement d'Hématologie et Immunologie biologiques, Hôpital Henri-Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, France.
Emmanuel BenayounDépartement d'Hématologie et Immunologie biologiques, Hôpital Henri-Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, France.
Daniel LusinaLaboratoire d'Hématologie, Hôpital Avicenne, Assistance Publique-Hôpitaux de Paris, Université Sorbonne Paris Cité, Bobigny, France.
Isabel GarciaLaboratoire d'Hématologie, Hôpital André Mignot, Centre Hospitalier de Versailles, Le Chesnay, France.
Claude GardinDépartement d'Hématologie Clinique, Hôpital Avicenne, Assistance Publique-Hôpitaux de Paris, Bobigny, France.
Pierre FenauxDépartement d'Hématologie Clinique, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France.
Cécile PautasDépartement d'Hématologie clinique, Hôpital Henri-Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, France.
Bruno QuesnelCHU Lille, Service des Maladies du Sang, 59000, Lille, France.
Pascal TurlureDépartement d'Hématologie Clinique, CHU Limoges, Limoges, France.
Christine TerréLaboratoire de Cytogénétique, Hôpital André Mignot, Centre Hospitalier de Versailles, Le Chesnay, France.
Xavier ThomasDépartement d'Hématologie Clinique, Hospices Civils de Lyon, Hôpital Lyon-Sud, Pierre Bénite, France.
Juliette LambertDépartement d'Hématologie Clinique, Hôpital André Mignot, Centre Hospitalier de Versailles, Le Chesnay, France.
Aline RennevilleService d'Hématologie Biologique, CHU Lille, Lille, France.ORCID http://orcid.org/0000-0003-0805-9640
Claude PreudhommeUniversité Lille, CNRS, INSERM, CHU Lille, IRCL, UMR9020 - UMR1277 - Canther - Cancer Heterogeneity, Plasticity and Resistance to Therapies, 59000, Lille, France.
Hervé DombretDépartement d'Hématologie Clinique, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, EA-3518, Institut de Recherche Saint-Louis, Université de Paris, Paris, France.
Raphael Itzykson *Université de Paris, Génomes, biologie cellulaire et thérapeutique U944, INSERM, CNRS, 75010, Paris, France. raphael.itzykson@aphp.fr.ORCID http://orcid.org/0000-0003-2139-6262
Thomas Cluzeau *Département d'Hématologie, Université Côte d'Azur, CHU de Nice, Nice, France. cluzeau.t@chu-nice.fr.ORCID http://orcid.org/0000-0002-6745-1127
Centre National de la Recherche Scientifique · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Lille · FRHôpital André Mignot · FRUniversité Paris Cité · FRCentre Hospitalier Universitaire de Limoges · FRHospices Civils de Lyon · FRInserm · FRUniversité Côte d'Azur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The independent prognostic impact of specific dysplastic features in acute myeloid leukemia (AML) remains controversial and may vary between genomic subtypes. We apply a machine learning framework to dissect the relative contribution of centrally reviewed dysplastic features and oncogenetics in 190 patients with de novo AML treated in ALFA clinical trials. One hundred and thirty-five (71%) patients achieved complete response after the first induction course (CR). Dysgranulopoiesis, dyserythropoiesis and dysmegakaryopoiesis were assessable in 84%, 83% and 63% patients, respectively. Multi-lineage dysplasia was present in 27% of assessable patients. Micromegakaryocytes (q = 0.01), hypolobulated megakaryocytes (q = 0.08) and hyposegmented granulocytes (q = 0.08) were associated with higher ELN-2017 risk. Using a supervised learning algorithm, the relative importance of morphological variables (34%) for the prediction of CR was higher than demographic (5%), clinical (2%), cytogenetic (25%), molecular (29%), and treatment (5%) variables. Though dysplasias had limited predictive impact on survival, a multivariate logistic regression identified the presence of hypolobulated megakaryocytes (p = 0.014) and micromegakaryocytes (p = 0.035) as predicting lower CR rates, independently of monosomy 7 (p = 0.013), TP53 (p = 0.004), and NPM1 mutations (p = 0.025). Assessment of these specific dysmegakarypoiesis traits, for which we identify a transcriptomic signature, may thus guide treatment allocation in AML.

Indexed as

AdultAgedAntineoplastic AgentsCytogenetic AnalysisFemaleHumansLeukemia, Myeloid, AcuteMachine LearningMaleMegakaryocytesMiddle AgedPrognosisTreatment OutcomeAntineoplastic Agents

Identifiers

PMID34615986
OpenAlexW3204419783

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.