4.7 Article

Disease Risk Comorbidity Index for Patients Receiving Haploidentical Allogeneic Hematopoietic Transplantation

期刊

ENGINEERING
卷 7, 期 2, 页码 162-169

出版社

ELSEVIER
DOI: 10.1016/j.eng.2020.12.005

关键词

Disease risk index; Disease risk comorbidity index; Hematopoietic cell transplantation comorbidity index; Hematopoietic stem cell transplantation; Haploidentical

资金

  1. National Key Research and Development Program of China [2017YFA0104500]
  2. Foundation for Innovative Research Groups of the National Natural Science Foundation of China [81621001]
  3. National Natural Science Foundation of China [81930004]
  4. Capital's Funds for Health Improvement and Research [2018-4-4089]
  5. CAMS Innovation Fund for Medical Sciences (CIFMS) [2019-I2M-5-034]
  6. Science and Technology Project of Guangdong Province of China [2016B030230003]
  7. Project of Health Collaborative Innovation of Guangzhou City [201704020214]
  8. Peking University Clinical Scientist Program [BMU2019LCKXJ003]
  9. Fundamental Research Funds for the Central Universities

向作者/读者索取更多资源

The development of Disease Risk Comorbidity Index (DRCI) based on Disease Risk Index (DRI) and Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) allows for effective risk stratification of patients receiving haploidentical hematopoietic stem cell transplantation. The DRCI accurately predicts disease-free survival, particularly in disease-specific subgroups such as acute leukemia patients. This index also shows predictive value for relapse, non-relapse mortality, overall survival, and can aid in identifying patients who will benefit most from the transplantation procedure.
We aimed to develop a disease risk comorbidity index (DRCI) based on disease risk index (DRI) and Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) in patients receiving haploidentical hematopoietic stem cell transplantation (haplo-HSCT). We identified the prognostic factors of disease-free survival (DFS) in a training subset (n = 593), then assigned a weighted score using these factors to the remaining patients (validation subset; n = 296). The multivariable model identified two independent predictors of DFS: DRI and HCT-CI before transplantation. In this scoring system, we assigned a weighted score of 2 to very high-risk DRI, and assigned a weighted score of 1 to high-risk DRI and intermediate- and high-risk HCT-CI (i.e., haplo-DRCI). In the validation cohort, the three-year DFS rate was 65.2% (95% confidence interval (CI), 58.2%-72.2%), 55.8% (95% CI, 44.9%-66.7%), and 32.0% (95% CI, 5.8%-58.2%) for the low-, intermediate-, and high-risk group, respectively (P = 0.005). Haplo-DRCI can also predict DFS in disease-specific subgroups, particularly in acute leukemia patients. Increasing score was also significantly predictive of increased relapse, increased non-relapse mortality (NRM), decreased DFS, and decreased overall survival (OS) in an independent historical cohort (n = 526). These data confirmed that haplo-DRCI could effectively risk stratify haplo-HSCT recipients and provide a tool to better predict who will best benefit from haplo-HSCT. (C) 2020 THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company.

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