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      Multi-centre validation of the prognostic value of the haematopoietic cell transplantation- specific comorbidity index among recipient of allogeneic haematopoietic cell transplantation.

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          Abstract

          The haematopoietic cell transplantation-specific comorbidity index (HCT-CI) was developed in a single centre as a weighted scoring system to predict risks of non-relapse mortality (NRM) following allogeneic haematopoietic cell transplantation. Information on the performance of the HCT-CI in multi-centre studies is lacking in the literature. To that end, a collaborative multicentre retrospective study was initiated. Comorbidity data from 2523 consecutive recipients of human leucocyte antigen-matched grafts from five different US institutions were analysed. Among all patients, HCT-CI scores of 0 vs. 1-2 vs. ≥3 were associated with 2-year NRM rates of 14%, 23% and 39% (P < 0·0001), respectively, and 2-year overall survival (OS) rates of 74%, 61% and 39%, respectively (P < 0·0001). Using regression models, increasing HCT-CI scores were independently associated with increases in hazard ratios for NRM and worse survival within individual institutions. The HCT-CI retained independent capacity for association with outcomes within different age as well as conditioning intensity groups. C-statistic estimates for the prognostic power of the HCT-CI for NRM and OS were 0·66 and 0·64, respectively. The estimates within each institution were overall similar. The HCT-CI is a valid tool for capturing comorbidities and predicting mortality after haematopoietic cell transplantation across different institutions.

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          Author and article information

          Journal
          Br. J. Haematol.
          British journal of haematology
          Wiley-Blackwell
          1365-2141
          0007-1048
          Aug 2015
          : 170
          : 4
          Affiliations
          [1 ] Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
          [2 ] National Cancer Institute, Cairo University, Cairo, Egypt.
          [3 ] Clinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
          [4 ] Department of Biostatistics, University of Washington School of Public Health, Seattle, WA, USA.
          [5 ] Division of Hematology/Blood and Marrow Transplantation, University of Utah School of Medicine, Logan, UT, USA.
          [6 ] Pediatric Blood and Marrow Transplant Program, Primary Children's Medical Center, Huntsman Cancer Institute, Salt Lake City, UT, USA.
          [7 ] Center for Hematologic Malignancies, OHSU Knight Cancer Institute, Portland, OR, USA.
          [8 ] Division of Hematology and Medical Oncology, Oregon Health & Science University School of Medicine, Portland, OR, USA.
          [9 ] Department of Population Sciences, Center for Cancer Survivorship, City of Hope School of Medicine, Duarte, CA, USA.
          [10 ] Colorado Blood Cancer Institute School of Medicine, Denver, CO, USA.
          [11 ] Department of Psychiatry and Behavioral Sciences, University of Washington School of Medicine Seattle, Seattle, WA, USA.
          [12 ] Division of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.
          Article
          NIHMS686605
          10.1111/bjh.13476
          4526353
          25945807
          79f5f64b-88aa-46f9-b6fc-9b8fe065e3c1
          History

          validation,HCT-CI,haematopoietic cell transplantation,comorbidities,allogeneic

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