Your browser doesn't support javascript.
loading
An adapted European LeukemiaNet genetic risk stratification for acute myeloid leukemia patients undergoing allogeneic hematopoietic cell transplant. A CIBMTR analysis.
Jimenez Jimenez, Antonio M; De Lima, Marcos; Komanduri, Krishna V; Wang, Trent P; Zhang, Mei-Jie; Chen, Karen; Abdel-Azim, Hisham; Abid, Muhammad Bilal; Aljurf, Mahmoud; Alkhateeb, Hassan; Assal, Amer; Bacher, Ulrike; Baron, Frédéric; Battiwalla, Minoo; Beitinjaneh, Amer; Bejanyan, Nelli; Bhatt, Vijaya Raj; Byrne, Michael; Cahn, Jean-Yves; Cairo, Mitchell; Castillo, Paul; Copelan, Edward; DeFilipp, Zachariah; Perez, Miguel Angel Diaz; Elsawy, Mahmoud; Gale, Robert Peter; George, Biju; Grunwald, Michael R; Hildebrandt, Gerhard C; Hogan, William J; Kanakry, Christopher G; Kansagra, Ankit; Kharfan-Dabaja, Mohamed A; Khera, Nandita; Krem, Maxwell M; Lazaryan, Aleksandr; Maakaron, Joseph; Martino, Rodrigo; McGuirk, Joseph; Michelis, Fotios V; Milone, Giuseppe; Mishra, Asmita; Murthy, Hemant S; Mussetti, Alberto; Nathan, Sunita; Nishihori, Taiga; Olsson, Richard F; Palmisiano, Neil; Patel, Sagar; Saad, Ayman.
Afiliación
  • Jimenez Jimenez AM; Division of Transplantation and Cellular Therapy, University of Miami Miller School of Medicine, Miami, FL, USA. amjimenez@med.miami.edu.
  • De Lima M; Department of Medicine, Seidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH, USA.
  • Komanduri KV; Division of Transplantation and Cellular Therapy, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Wang TP; Division of Transplantation and Cellular Therapy, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Zhang MJ; (CIBMTR)® Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Chen K; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Abdel-Azim H; (CIBMTR)® Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Abid MB; Division of Hematology, Oncology and Blood & Marrow Transplantation, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, CA, USA.
  • Aljurf M; Divisions of Hematology/Oncology & Infectious Diseases, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Alkhateeb H; Department of Oncology, King Faisal Specialist Hospital Center & Research, Riyadh, Saudi Arabia.
  • Assal A; Mayo Clinic Rochester, Rochester, MN, USA.
  • Bacher U; Columbia University Irving Medical Center, Department of Medicine, Bone Marrow Transplant and Cell Therapy Program, New York, NY, USA.
  • Baron F; Department of Hematology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
  • Battiwalla M; CHU and University of Liege, Liege, Belgium.
  • Beitinjaneh A; Sarah Cannon Blood Cancer Network, Nashville, TN, USA.
  • Bejanyan N; Division of Transplantation and Cellular Therapy, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Bhatt VR; Department of Blood & Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, FL, USA.
  • Byrne M; The Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, USA.
  • Cahn JY; Vanderbilt University Medical Center, Nashville, TN, USA.
  • Cairo M; Department of Hematology, CHU Grenoble Alpes, Université Grenoble Alpes, Grenoble, France.
  • Castillo P; Division of Pediatric Hematology, Oncology and Stem Cell Transplantation, Department of Pediatrics, New York Medical College, Valhalla, NY, USA.
  • Copelan E; UF Health Shands Children's Hospital, Gainesville, FL, USA.
  • DeFilipp Z; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Perez MAD; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA, USA.
  • Elsawy M; Department of Hematology/Oncology, Hospital Infantil Universitario Niño Jesus, Madrid, Spain.
  • Gale RP; Division of Hematology, Department of Medicine, Dalhousie University, Halifax, Canada.
  • George B; Haematology Research Centre, Department of Immunology and Inflammation, Imperial College London, London, UK.
  • Grunwald MR; Christian Medical College, Vellore, India.
  • Hildebrandt GC; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Hogan WJ; Markey Cancer Center, University of Kentucky, Lexington, KY, USA.
  • Kanakry CG; Division of Hematology/BMT, Mayo Clinic, Rochester, MN, USA.
  • Kansagra A; Experimental Transplantation and Immunotherapy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Kharfan-Dabaja MA; UT Southwestern Medical Center, Blood and Marrow Transplant Program, Dallas, TX, USA.
  • Khera N; Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL, USA.
  • Krem MM; Department of Hematology/Oncology, Mayo Clinic, Phoenix, AZ, USA.
  • Lazaryan A; Markey Cancer Center, University of Kentucky College of Medicine, Lexington, KY, USA.
  • Maakaron J; Department of Blood & Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, FL, USA.
  • Martino R; Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.
  • McGuirk J; Divison of Clinical Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Michelis FV; Division of Hematologic Malignancies and Cellular Therapeutics, The University of Kansas Cancer Center, Minneapolis, MN, USA.
  • Milone G; Allogeneic Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, Toronto, Canada.
  • Mishra A; Azienda Ospedaliera Universitaria Policlinico-San Marco, Catania, Italy.
  • Murthy HS; Department of Blood & Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, FL, USA.
  • Mussetti A; Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL, USA.
  • Nathan S; Hematology Department, Institut Catalá d' Oncologia-Hospitalet, Barcelona, Spain.
  • Nishihori T; IDIBELL-Institut Catalá d' Oncologia, l'Hospitalet de Llobregat, El Prat de Llobregat, Spain.
  • Olsson RF; Section of Bone Marrow Transplant and Cell Therapy, Rush University Medical Center, Chicago, IL, USA.
  • Palmisiano N; Department of Blood & Marrow Transplant and Cellular Immunotherapy (BMT CI), Moffitt Cancer Center, Tampa, FL, USA.
  • Patel S; Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Saad A; Centre for Clinical Research Sormland, Uppsala University, Uppsala, Sweden.
Bone Marrow Transplant ; 56(12): 3068-3077, 2021 12.
Article en En | MEDLINE | ID: mdl-34584240
ABSTRACT
Cytogenetic and molecular abnormalities are known to influence post-transplant outcomes in acute myeloid leukemia (AML) but data assessing the prognostic value of combined genetic models in the HCT setting are limited. We developed an adapted European LeukemiaNet (aELN) risk classification based on available genetic data reported to the Center for International Blood and Marrow Transplant Research, to predict post-transplant outcomes in 2289 adult AML patients transplanted in first remission, between 2013 and 2017. Patients were stratified according to aELN into three groups favorable (Fav, N = 181), intermediate (IM, N = 1185), and adverse (Adv, N = 923). Univariate analysis demonstrated significant differences in 2-year overall survival (OS) (Fav 67.7%, IM 64.9% and Adv 53.9%; p < 0.001); disease-free survival (DFS) (Fav 57.8%, IM 55.5% and Adv 45.3; p < 0.001) and relapse (Fav 28%, IM 27.5% and Adv 37.5%; p < 0.001). Multivariate analysis (MVA) revealed no differences in outcomes between the Fav and IM groups, thus they were combined. On MVA, patients in the Adv risk group had the highest risk of relapse (HR 1.47 p ≤ 0.001) and inferior DFS (HR 1.35 p < 0.001) and OS (HR 1.39 p < 0.001), even using myeloablative conditioning or in those without the pre-HCT measurable-residual disease. Novel approaches to mitigate relapse in this high-risk group are urgently needed.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos