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The Hematopoietic Cell Transplant Comorbidity Index predicts survival after allogeneic transplant for nonmalignant diseases.
Thakar, Monica S; Broglie, Larisa; Logan, Brent; Artz, Andrew; Bunin, Nancy; Burroughs, Lauri M; Fretham, Caitrin; Jacobsohn, David A; Loren, Alison W; Kurtzberg, Joanne; Martinez, Caridad A; Mineishi, Shin; Nelson, Adam S; Woolfrey, Ann; Pasquini, Marcelo C; Sorror, Mohamed L.
Afiliación
  • Thakar MS; Division of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, Department of Pediatrics, and.
  • Broglie L; Division of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, Department of Pediatrics, and.
  • Logan B; Division of Biostatistics, Medical College of Wisconsin, Milwaukee, WI.
  • Artz A; Section of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL.
  • Bunin N; Cellular Therapy and Transplant Section, Division of Oncology, Department of Pediatrics, The Children's Hospital of Philadelphia, Pennsylvania, PA.
  • Burroughs LM; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Fretham C; Division of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, Department of Pediatrics, University of Washington, Seattle, WA.
  • Jacobsohn DA; Division of Biostatistics, Center for International Blood and Marrow Transplant Research, National Marrow Donor Program, Minneapolis, MN.
  • Loren AW; Division of Blood and Marrow Transplantation, Department of Pediatrics, Children's National Health System and George Washington University, Washington, DC.
  • Kurtzberg J; Division of Hematology Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Martinez CA; Division of Pediatric Blood and Marrow Transplant, Department of Pediatrics, Duke University Medical Center, Durham, NC.
  • Mineishi S; Center for Cell and Gene Therapy, Baylor College of Medicine and Texas Children's Hospital, Houston, TX.
  • Nelson AS; Blood and Marrow Transplant Program, Division of Hematology and Oncology, Department of Medicine, Penn State Hershey Medical Center, Hershey, PA.
  • Woolfrey A; Division of Bone Marrow Transplant and Immune Deficiency, Department of Pediatrics, Cincinnati Children's Hospital, Cincinnati, OH.
  • Pasquini MC; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Sorror ML; Division of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, Department of Pediatrics, University of Washington, Seattle, WA.
Blood ; 133(7): 754-762, 2019 02 14.
Article en En | MEDLINE | ID: mdl-30545834
ABSTRACT
Despite improvements, mortality after allogeneic hematopoietic cell transplantation (HCT) for nonmalignant diseases remains a significant problem. We evaluated whether pre-HCT conditions defined by the HCT Comorbidity Index (HCT-CI) predict probability of posttransplant survival. Using the Center for International Blood and Marrow Transplant Research database, we identified 4083 patients with nonmalignant diseases transplanted between 2007 and 2014. Primary outcome was overall survival (OS) using the Kaplan-Meier method. Hazard ratios (HRs) were estimated by multivariable Cox regression models. Increasing HCT-CI scores translated to decreased 2-year OS of 82.7%, 80.3%, 74%, and 55.8% for patients with HCT-CI scores of 0, 1 to 2, 3 to 4, and ≥5, respectively, regardless of conditioning intensity. HCT-CI scores of 1 to 2 did not differ relative to scores of 0 (HR, 1.12 [95% CI, 0.93-1.34]), but HCT-CI of 3 to 4 and ≥5 posed significantly greater risks of mortality (HR, 1.33 [95% CI, 1.09-1.63]; and HR, 2.31 [95% CI, 1.79-2.96], respectively). The effect of HCT-CI differed by disease indication. Patients with acquired aplastic anemia, primary immune deficiencies, and congenital bone marrow failure syndromes with scores ≥3 had increased risk of death after HCT. However, higher HCT-CI scores among hemoglobinopathy patients did not increase mortality risk. In conclusion, this is the largest study to date reporting on patients with nonmalignant diseases demonstrating HCT-CI scores ≥3 that had inferior survival after HCT, except for patients with hemoglobinopathies. Our findings suggest that using the HCT-CI score, in addition to disease-specific factors, could be useful when developing treatment plans for nonmalignant diseases.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Enfermedades de la Médula Ósea / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped / Hemoglobinuria Paroxística / Anemia Aplásica / Enfermedades Metabólicas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Blood Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Enfermedades de la Médula Ósea / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped / Hemoglobinuria Paroxística / Anemia Aplásica / Enfermedades Metabólicas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Blood Año: 2019 Tipo del documento: Article