Your browser doesn't support javascript.
loading
Risk score to predict event-free survival after hematopoietic cell transplant for sickle cell disease.
Brazauskas, Ruta; Scigliuolo, Graziana M; Wang, Hai-Lin; Cappelli, Barbara; Ruggeri, Annalisa; Fitzhugh, Courtney D; Hankins, Jane S; Kanter, Julie; Meerpohl, Joerg J; Panepinto, Julie A; Rondelli, Damiano; Shenoy, Shalini; Walters, Mark C; Wagner, John E; Tisdale, John F; Gluckman, Eliane; Eapen, Mary.
Affiliation
  • Brazauskas R; Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, WI.
  • Scigliuolo GM; Monacord, Centre Scientifique de Monaco, Monaco, Monaco.
  • Wang HL; Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
  • Cappelli B; Monacord, Centre Scientifique de Monaco, Monaco, Monaco.
  • Ruggeri A; Hematology and Bone Marrow Transplant Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Fitzhugh CD; Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.
  • Hankins JS; Department of Hematology, St. Jude Children's Research Hospital, Memphis, TN.
  • Kanter J; Division of Hematology and Oncology, Department of Medicine, University of Alabama, Birmingham, AL.
  • Meerpohl JJ; Institute for Evidence in Medicine, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Panepinto JA; Department of Pediatrics, Medical College of Wisconsin/Children's of Wisconsin, Milwaukee, WI.
  • Rondelli D; Division of Hematology/Oncology, University of Illinois at Chicago, Chicago, IL.
  • Shenoy S; Department of Pediatrics, Washington University, St. Louis, MO.
  • Walters MC; University of California San Francisco Benioff Children's Hospital, Oakland CA.
  • Wagner JE; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN; and.
  • Tisdale JF; Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.
  • Gluckman E; Monacord, Centre Scientifique de Monaco, Monaco, Monaco.
  • Eapen M; Eurocord, Université de Paris, Institut de Recherche de Saint-Louis, Paris, France.
Blood ; 136(5): 623-626, 2020 07 30.
Article in En | MEDLINE | ID: mdl-32518950
We developed a risk score to predict event-free survival (EFS) after allogeneic hematopoietic cell transplantation for sickle cell disease. The study population (n = 1425) was randomly split into training (n = 1070) and validation (n = 355) cohorts. Risk factors were identified and validated via Cox regression models. Two risk factors of 9 evaluated were predictive for EFS: age at transplantation and donor type. On the basis of the training cohort, patients age 12 years or younger with an HLA-matched sibling donor were at the lowest risk with a 3-year EFS of 92% (score, 0). Patients age 13 years or older with an HLA-matched sibling donor or age 12 years or younger with an HLA-matched unrelated donor were at intermediate risk (3-year EFS, 87%; score, 1). All other groups, including patients of any age with a haploidentical relative or HLA-mismatched unrelated donor and patients age 13 years or older with an HLA-matched unrelated donor were high risk (3-year EFS, 57%; score, 2 or 3). These findings were confirmed in the validation cohort. This simple risk score may guide patients with sickle cell disease and hematologists who are considering allogeneic transplantation as a curative treatment relative to other available contemporary treatments.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Anemia, Sickle Cell Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2020 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Anemia, Sickle Cell Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2020 Document type: Article Country of publication: United States