Evidence map›Paper›PMID 37841754›Full record

ArticleHemaSphere2023

Machine Learning Improves Risk Stratification in Myelodysplastic Neoplasms: An Analysis of the Spanish Group of Myelodysplastic Syndromes.

Adrian Mosquera Orgueira, Manuel Mateo Perez Encinas, Nicolas A Diaz Varela, Elvira Mora, Marina Díaz-Beyá, María Julia Montoro, Helena Pomares, Fernando Ramos, Mar Tormo, Andres Jerez and 12 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 16 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

22 authors at 18 institutions in 1 country.

Adrian Mosquera OrgueiraComplexo Hospitalario Universitario de Santiago de Compostela, Department of Hematology, Instituto de Investigacións Sanitarias de Santiago, Santiago de Compostela, Spain.
Manuel Mateo Perez EncinasComplexo Hospitalario Universitario de Santiago de Compostela, Department of Hematology, Instituto de Investigacións Sanitarias de Santiago, Santiago de Compostela, Spain.
Nicolas A Diaz VarelaHospital Central de Asturias, Oviedo, Spain.
Elvira MoraHematology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.ORCID https://orcid.org/0000-0003-3361-8803
Marina Díaz-BeyáHospital Clinic, Dept. of Hematology, IDIBAPS, Barcelona, Spain.
María Julia MontoroDepartment of Hematology, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Helena PomaresHematology Department., Hospital Duran i Reynals. Institut Català d'Oncologia, Hospital Duran i Reynals. Institut Català d'Oncologia, Hospitalet, Barcelona, Spain.
Fernando RamosDepartment of Hematology, Hospital Universitario de León, Spain.
Mar TormoServicio de Hematología. Hospital Clínico Universitario de Valencia, Spain.
Andres JerezHematology and Medical Oncology Department, Hospital Morales Meseguer, IMIB, Murcia, Spain.
Josep F NomdedeuHematology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Carlos De Miguel SanchezHospital Universitario de Álava - Sede Txagorritxu, Vitoria-Gasteiz, Spain.
Arenillas LeonorLaboratoris de Citologia Hematològica i Citogenètica, servei de Patologia, Hospital del Mar. GRETNHE- Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain.
Paula CárcelDepartment of Hematology, Hospital Público Universitario de la Ribera, Alzira, Valencia, Spain.
Maria Teresa Cedena RomeroHospital Universitario 12 de Octubre, Instituto de Investigación Sanitaria i+12, Madrid, Spain.
Blanca XicoyHU German Trias i Pujol - Institut Català d' Oncologia, Josep Carreras Leukemia Research Institute, Universitat Autònoma de Barcelona, Badalona, Spain.
Eugenia RiveroDepartment of Hematology, University Hospital Arnau de Vilanova, Lleida, Spain.
Rafael Andres Del Orbe BarretoEdif. Laboratorios, planta baja., Hospital Universitario Cruces Servicio de Hematología. Sección Eritropatología - Hem. Molecular, Barakaldo, Spain.
Maria Diez-CampeloHematology Department, Institute of Biomedical Research of Salamanca, University Hospital of Salamanca, Spain.
Luis E BenllochGrupo Español de Síndromes Mielodisplásicos (GESMD), Valencia, Spain.
Davide CrucittiInstituto de Investigacions Sanitarias de Santiago de Compostela (IDIS-CHUS), Santiago de Compostela, Spain.
David ValcárcelDepartment of Hematology, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Instituto de Investigación Sanitaria de Santiago · ESVall d'Hebron Hospital Universitari · ESHospital Clínic de Barcelona · ESHospital Clínico Universitario de Valencia · ESHospital de Cruces · ESHospital de La Ribera · ESHospital de León · ESHospital del Mar Research Institute · ESHospital de Sant Pau · ESHospital General Universitario Morales Meseguer · ESHospital Txagorritxu · ESHospital Universitari Arnau de Vilanova · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario 12 De Octubre · ESHospital Universitario Central de Asturias · ESInstitut Català d'Oncologia · ESUniversidad de Salamanca · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelodysplastic neoplasms (MDS) are a heterogeneous group of hematological stem cell disorders characterized by dysplasia, cytopenias, and increased risk of acute leukemia. As prognosis differs widely between patients, and treatment options vary from observation to allogeneic stem cell transplantation, accurate and precise disease risk prognostication is critical for decision making. With this aim, we retrieved registry data from MDS patients from 90 Spanish institutions. A total of 7202 patients were included, which were divided into a training (80%) and a test (20%) set. A machine learning technique (random survival forests) was used to model overall survival (OS) and leukemia-free survival (LFS). The optimal model was based on 8 variables (age, gender, hemoglobin, leukocyte count, platelet count, neutrophil percentage, bone marrow blast, and cytogenetic risk group). This model achieved high accuracy in predicting OS (c-indexes; 0.759 and 0.776) and LFS (c-indexes; 0.812 and 0.845). Importantly, the model was superior to the revised International Prognostic Scoring System (IPSS-R) and the age-adjusted IPSS-R. This difference persisted in different age ranges and in all evaluated disease subgroups. Finally, we validated our results in an external cohort, confirming the superiority of the Artificial Intelligence Prognostic Scoring System for MDS (AIPSS-MDS) over the IPSS-R, and achieving a similar performance as the molecular IPSS. In conclusion, the AIPSS-MDS score is a new prognostic model based exclusively on traditional clinical, hematological, and cytogenetic variables. AIPSS-MDS has a high prognostic accuracy in predicting survival in MDS patients, outperforming other well-established risk-scoring systems.

Identifiers

PMID37841754
PMCPMC10569758
OpenAlexW4387574400

What OpenQuestion holds

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LicenceCC BY
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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.