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Hematopoietic Cell Transplantation Comorbidity Index Predicts Outcomes in Patients with Acute Myeloid Leukemia and Myelodysplastic Syndromes Receiving CD34+ Selected Grafts for Allogeneic Hematopoietic Cell Transplantation
Authors:Pere Barba,Ravin Ratan,Christina Cho,Izaskun Ceberio,Patrick Hilden,Sean M. Devlin,Molly A. Maloy,Juliet N. Barker,Hugo Castro-Malaspina,Ann A. Jakubowski,Guenther Koehne,Esperanza B. Papadopoulos,Doris M. Ponce,Craig Sauter,Roni Tamari,Marcel R.M. van den Brink,James W. Young,Richard J. O&#x  Reilly,Miguel-Angel Perales
Affiliation:1. Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York;2. Hematology Department, Hospital Universitario Vall d''Hebron-Universidad Autonoma de Barcelona, Barcelona, Spain;3. Department of Medicine, Weill Cornell Medical College, New York, New York;4. Hematology Department of Hospital Universitario Donostia, Donostia, Spain;5. Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York;6. Department of Pediatrics, Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York
Abstract:
To evaluate the association between the hematopoietic cell transplantation-comorbidity index (HCT-CI) and the recently developed age-adjusted HCT-CI (HCT-CI/age) and transplant outcomes in the setting of CD34-selected allogeneic HCT, we analyzed a homogeneous population of patients undergoing allogeneic HCT with CD34-selected grafts for acute myeloid leukemia and myelodysplastic syndrome (n?=?346). Median HCT-CI and HCT-CI/age scores were 2 (percentile 25 to 75, 1 to 4) and 3 (percentile 25 to 75, 1 to 5), respectively. Higher HCT-CI and HCT-CI/age scores were associated with higher nonrelapse mortality (NRM) and lower overall survival (OS). The HCT-CI distinguished 2 risk groups (0 to 2 versus ≥3), whereas, with the HCT-CI/age, there was a progressive increase in NRM and decrease in OS with increasing scores in all 4 groups (0 versus 1 to 2 versus 3 to 4 versus ≥5). Higher scores in both models were associated with lower chronic graft-versus-host disease relapse-free survival but not with higher relapse. Both models showed a promising predictive accuracy for NRM (c??= .616 for HCT-CI and c??=?.647 for HCT-CI/age). In conclusion, the HCT-CI and HCT-CI/age predict transplant outcomes in CD34-selected allo-HCT, including NRM, OS, and chronic graft-versus-host disease relapse-free survival and may be used to select appropriate patients for this approach.
Keywords:HCT-CI  T cell depletion  Allogeneic hematopoietic cell transplantation  Comorbidity
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