Evidence map›Paper›PMID 38007531›Full record

ArticleBone marrow transplantation2024

Artificial intelligence methods to estimate overall mortality and non-relapse mortality following allogeneic HCT in the modern era: an EBMT-TCWP study.

A Mussetti, B Rius-Sansalvador, V Moreno, C Peczynski, E Polge, J E Galimard, N Kröger, D Blaise, R Peffault de Latour, A Kulagin and 25 more

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Article in Bone marrow transplantation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Trial
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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

35 authors.

A Mussetti *Department of Haematology, Institut Català d'Oncologia - Hospitalet, IDIBELL, University of Barcelona, Barcelona, Spain. amussetti@iconcologia.net.
B Rius-Sansalvador *Biomarkers and Susceptibility Unit (UBS), Oncology Data Analytics Program (ODAP), Catalan Institute of Oncology (ICO), L'Hospitalet del Llobregat, Barcelona, Spain.ORCID 0000-0001-9864-2906
V MorenoBiomarkers and Susceptibility Unit (UBS), Oncology Data Analytics Program (ODAP), Catalan Institute of Oncology (ICO), L'Hospitalet del Llobregat, Barcelona, Spain.
C PeczynskiEBMT Paris Study Office, Department of Haematology, Saint Antoine Hospital, INSERM Unité Mixte de Recherche (UMR)-S 938, Sorbonne University, Paris, France.ORCID 0000-0002-3829-0088
E PolgeEBMT Global Committee (Shanghai and Paris Offices) and Acute Leukaemia Working Party, Hospital Saint-Antoine APHP and Sorbonne University, Paris, France.
J E GalimardEBMT, Statistics Unit, Paris, France.ORCID 0000-0001-9102-4427
N KrögerDepartment of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-5103-9966
D BlaiseProgramme de Transplantation & Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.ORCID 0000-0002-5684-9447
R Peffault de LatourService d'Hématologie-Greffe, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.
A KulaginRaisa Memorial (RM) Gorbacheva Research Institute, Pavlov University, St. Petersburg, Russia.ORCID 0000-0002-9589-4136
A MousaviShariati Hospital, Haematology-Oncology and BMT Research, Tehran, Islamic Republic of Iran.
M StelljesDepartment of Medicine A, University Hospital Münster, Münster, Germany.
R M HamladjiCentre Pierre et Marie Curie, Service Hématologie Greffe de Moëlle, Alger, Algeria.
J M MiddekeMed. Klinik I, University Hospital, TU Dresden, Germany.
U SalmenniemiHUCH Comprehensive Cancer Center, Stem Cell Transplantation Unit, Helsinki, Finland.
H SengeloevBone Marrow Transplant Unit Copenhagen, Department of Haematology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
E ForcadeCHU Bordeaux, Service d'hématologie Clinique et Thérapie Cellulaire, 33000, Pessac, France.ORCID 0000-0002-8873-2868
U PlatzbeckerUniversity Hospital Leipzig, Leipzig, Germany.
P ReményiDepartment of Haematology and Stem Cell Transplant, Dél-pesti Centrumkórház - Országos Hematológiai és Infektológiai Intézet, Budapest, Hungary.
E AngelucciHaematology and Cellular Therapy Unit. IRCCS Ospedale Policlinico San Martino, Genova, Italy.
P ChevallierCHU Nantes, Nantes, France.ORCID 0000-0003-3142-5581
I Yakoub-AghaCHU de Lille LIRIC, INSERM U995, Université de Lille, Lille, France.ORCID 0000-0003-4524-8782
C CraddockDepartment of Haematology, University Hospital Birmingham NHS Trust, Queen Elizabeth Medical Centre, Edgbaston, Birmingham, UK.ORCID 0000-0001-5041-6678
F CiceriHaematology & Bone Marrow Transplant, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0003-0873-0123
T SchroederDepartment of Bone Marrow Transplantation, University Hospital, Essen, Germany.
M AljurfOncology Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.ORCID 0000-0003-3942-7370
Koenecke ChHannover Medical School, Hannover, Germany.ORCID 0000-0001-7025-1735
I MoiseevR.M.Gorbacheva Memorial Institute of Oncology, Haematology and Transplantation, Pavlov First Saint Petersburg State Medical University, Saint-Petersburg, Russian Federation.ORCID 0000-0002-4332-0114
O PenackDepartment of Haematology, Charité Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-4876-802X
H SchoemansDepartment of Haematology, University Hospitals Leuven, Leuven, Belgium.ORCID 0000-0002-7568-8239
M MohtyDepartment of Haematology, Saint Antoine Hospital, INSERM UMR 938, Sorbonne University, Paris, France.ORCID 0000-0002-7264-808X
B GlassKlinik für Hämatologie und Stammzelltransplantation, HELIOS Klinikum Berlin-Buch, Berlin, Germany.
A SuredaDepartment of Haematology, Institut Català d'Oncologia - Hospitalet, IDIBELL, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-1238-6970
G BasakDepartment of Haematology, Transplantation and Internal Medicine, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0003-3858-8180
Z PericSchool of medicine, University of Zagreb and University Hospital Centre Zagreb, Zagreb, Croatia.ORCID 0000-0001-9458-8025

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic haematopoietic cell transplantation (alloHCT) has curative potential counterbalanced by its toxicity. Prognostic scores fail to include current era patients and alternative donors. We examined adult patients from the EBMT registry who underwent alloHCT between 2010 and 2019 for oncohaematological disease. Our primary objective was to develop a new prognostic score for overall mortality (OM), with a secondary objective of predicting non-relapse mortality (NRM) using the OM score. AI techniques were employed. The model for OM was trained, optimized, and validated using 70%, 15%, and 15% of the data set, respectively. The top models, "gradient boosting" for OM (AUC = 0.64) and "elasticnet" for NRM (AUC = 0.62), were selected. The analysis included 33,927 patients. In the final prognostic model, patients with the lowest score had a 2-year OM and NRM of 18 and 13%, respectively, while those with the highest score had a 2-year OM and NRM of 82 and 93%, respectively. The results were consistent in the subset of the haploidentical cohort (n = 4386). Our score effectively stratifies the risk of OM and NRM in the current era but do not significantly improve mortality prediction. Future prognostic scores can benefit from identifying biological or dynamic markers post alloHCT.

Indexed as

Artificial IntelligenceHematopoietic Stem Cell TransplantationAdultChronic DiseaseHumansNeoplasm Recurrence, LocalPrognosisRetrospective StudiesTransplantation, Homologous

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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.