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Artificial intelligence methods to estimate overall mortality and non-relapse mortality following allogeneic HCT in the modern era: an EBMT-TCWP study.
Mussetti, A; Rius-Sansalvador, B; Moreno, V; Peczynski, C; Polge, E; Galimard, J E; Kröger, N; Blaise, D; Peffault de Latour, R; Kulagin, A; Mousavi, A; Stelljes, M; Hamladji, R M; Middeke, J M; Salmenniemi, U; Sengeloev, H; Forcade, E; Platzbecker, U; Reményi, P; Angelucci, E; Chevallier, P; Yakoub-Agha, I; Craddock, C; Ciceri, F; Schroeder, T; Aljurf, M; Ch, Koenecke; Moiseev, I; Penack, O; Schoemans, H; Mohty, M; Glass, B; Sureda, A; Basak, G; Peric, Z.
Afiliação
  • Mussetti A; Department of Haematology, Institut Català d'Oncologia - Hospitalet, IDIBELL, University of Barcelona, Barcelona, Spain. amussetti@iconcologia.net.
  • Rius-Sansalvador B; Biomarkers and Susceptibility Unit (UBS), Oncology Data Analytics Program (ODAP), Catalan Institute of Oncology (ICO), L'Hospitalet del Llobregat, Barcelona, Spain.
  • Moreno V; ONCOBELL Program, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
  • Peczynski C; Biomarkers and Susceptibility Unit (UBS), Oncology Data Analytics Program (ODAP), Catalan Institute of Oncology (ICO), L'Hospitalet del Llobregat, Barcelona, Spain.
  • Polge E; ONCOBELL Program, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
  • Galimard JE; EBMT Paris Study Office, Department of Haematology, Saint Antoine Hospital, INSERM Unité Mixte de Recherche (UMR)-S 938, Sorbonne University, Paris, France.
  • Kröger N; EBMT Global Committee (Shanghai and Paris Offices) and Acute Leukaemia Working Party, Hospital Saint-Antoine APHP and Sorbonne University, Paris, France.
  • Blaise D; EBMT, Statistics Unit, Paris, France.
  • Peffault de Latour R; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Kulagin A; Programme de Transplantation & Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.
  • Mousavi A; Service d'Hématologie-Greffe, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.
  • Stelljes M; Université Paris Diderot, Institut Universitaire d'Hématologie, Sorbonne Paris Cité, Paris, France.
  • Hamladji RM; Raisa Memorial (RM) Gorbacheva Research Institute, Pavlov University, St. Petersburg, Russia.
  • Middeke JM; Shariati Hospital, Haematology-Oncology and BMT Research, Tehran, Islamic Republic of Iran.
  • Salmenniemi U; Department of Medicine A, University Hospital Münster, Münster, Germany.
  • Sengeloev H; Centre Pierre et Marie Curie, Service Hématologie Greffe de Moëlle, Alger, Algeria.
  • Forcade E; Med. Klinik I, University Hospital, TU Dresden, Germany.
  • Platzbecker U; HUCH Comprehensive Cancer Center, Stem Cell Transplantation Unit, Helsinki, Finland.
  • Reményi P; Bone Marrow Transplant Unit Copenhagen, Department of Haematology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
  • Angelucci E; CHU Bordeaux, Service d'hématologie Clinique et Thérapie Cellulaire, 33000, Pessac, France.
  • Chevallier P; University Hospital Leipzig, Leipzig, Germany.
  • Yakoub-Agha I; Department of Haematology and Stem Cell Transplant, Dél-pesti Centrumkórház - Országos Hematológiai és Infektológiai Intézet, Budapest, Hungary.
  • Craddock C; Haematology and Cellular Therapy Unit. IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Ciceri F; CHU Nantes, Nantes, France.
  • Schroeder T; CHU de Lille LIRIC, INSERM U995, Université de Lille, Lille, France.
  • Aljurf M; Department of Haematology, University Hospital Birmingham NHS Trust, Queen Elizabeth Medical Centre, Edgbaston, Birmingham, UK.
  • Ch K; Haematology & Bone Marrow Transplant, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Moiseev I; Department of Bone Marrow Transplantation, University Hospital, Essen, Germany.
  • Penack O; Oncology Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Schoemans H; Hannover Medical School, Hannover, Germany.
  • Mohty M; R.M.Gorbacheva Memorial Institute of Oncology, Haematology and Transplantation, Pavlov First Saint Petersburg State Medical University, Saint-Petersburg, Russian Federation.
  • Glass B; Department of Haematology, Charité Universitätsmedizin Berlin, Berlin, Germany.
  • Sureda A; Department of Haematology, University Hospitals Leuven, Leuven, Belgium.
  • Basak G; Department of Public Health and Primary Care, ACCENT VV, KU Leuven - University of Leuven, Leuven, Belgium.
  • Peric Z; Department of Haematology, Saint Antoine Hospital, INSERM UMR 938, Sorbonne University, Paris, France.
Bone Marrow Transplant ; 59(2): 232-238, 2024 02.
Article em En | MEDLINE | ID: mdl-38007531
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Transplante de Células-Tronco Hematopoéticas Limite: Adult / Humans Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Transplante de Células-Tronco Hematopoéticas Limite: Adult / Humans Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha
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