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The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT

Individual comorbidities have distinct contributions to nonrelapse mortality (NRM) following allogeneic hematopoietic cell transplantation (allo-HCT). We studied the impact of comorbidities individually and in combination in a single-center cohort of 573 adult patients who underwent CD34-selected al...

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Autores principales: Shouval, Roni, Fein, Joshua A., Cho, Christina, Avecilla, Scott T., Ruiz, Josel, Tomas, Ana Alarcon, Sanchez-Escamilla, Miriam, Flores, Nerea Castillo, Yáñez, Lucrecia, Barker, Juliet N., Dahi, Parastoo, Giralt, Sergio A., Geyer, Alexander I., Gyurkocza, Boglarka, Jakubowski, Ann A., Lin, Richard J., O’Reilly, Richard J., Papadopoulos, Esperanza B., Politikos, Ioannis, Ponce, Doris M., Sauter, Craig S., Scordo, Michael, Shaffer, Brian, Shah, Gunjan L., Sullivan, James P., Tamari, Roni, van den Brink, Marcel R. M., Young, James W., Nagler, Arnon, Devlin, Sean, Shimoni, Avichai, Perales, Miguel-Angel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905694/
https://www.ncbi.nlm.nih.gov/pubmed/34507354
http://dx.doi.org/10.1182/bloodadvances.2021004319
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author Shouval, Roni
Fein, Joshua A.
Cho, Christina
Avecilla, Scott T.
Ruiz, Josel
Tomas, Ana Alarcon
Sanchez-Escamilla, Miriam
Flores, Nerea Castillo
Yáñez, Lucrecia
Barker, Juliet N.
Dahi, Parastoo
Giralt, Sergio A.
Geyer, Alexander I.
Gyurkocza, Boglarka
Jakubowski, Ann A.
Lin, Richard J.
O’Reilly, Richard J.
Papadopoulos, Esperanza B.
Politikos, Ioannis
Ponce, Doris M.
Sauter, Craig S.
Scordo, Michael
Shaffer, Brian
Shah, Gunjan L.
Sullivan, James P.
Tamari, Roni
van den Brink, Marcel R. M.
Young, James W.
Nagler, Arnon
Devlin, Sean
Shimoni, Avichai
Perales, Miguel-Angel
author_facet Shouval, Roni
Fein, Joshua A.
Cho, Christina
Avecilla, Scott T.
Ruiz, Josel
Tomas, Ana Alarcon
Sanchez-Escamilla, Miriam
Flores, Nerea Castillo
Yáñez, Lucrecia
Barker, Juliet N.
Dahi, Parastoo
Giralt, Sergio A.
Geyer, Alexander I.
Gyurkocza, Boglarka
Jakubowski, Ann A.
Lin, Richard J.
O’Reilly, Richard J.
Papadopoulos, Esperanza B.
Politikos, Ioannis
Ponce, Doris M.
Sauter, Craig S.
Scordo, Michael
Shaffer, Brian
Shah, Gunjan L.
Sullivan, James P.
Tamari, Roni
van den Brink, Marcel R. M.
Young, James W.
Nagler, Arnon
Devlin, Sean
Shimoni, Avichai
Perales, Miguel-Angel
author_sort Shouval, Roni
collection PubMed
description Individual comorbidities have distinct contributions to nonrelapse mortality (NRM) following allogeneic hematopoietic cell transplantation (allo-HCT). We studied the impact of comorbidities individually and in combination in a single-center cohort of 573 adult patients who underwent CD34-selected allo-HCT following myeloablative conditioning. Pulmonary disease, moderate to severe hepatic comorbidity, cardiac disease of any type, and renal dysfunction were associated with increased NRM in multivariable Cox regression models. A Simplified Comorbidity Index (SCI) composed of the 4 comorbidities predictive of NRM, as well as age >60 years, stratified patients into 5 groups with a stepwise increase in NRM. NRM rates ranged from 11.4% to 49.9% by stratum, with adjusted hazard ratios of 1.84, 2.59, 3.57, and 5.38. The SCI was also applicable in an external cohort of 230 patients who underwent allo-HCT with unmanipulated grafts following intermediate-intensity conditioning. The area under the receiver operating characteristic curve (AUC) of the SCI for 1-year NRM was 70.3 and 72.0 over the development and external-validation cohorts, respectively; corresponding AUCs of the Hematopoietic Cell Transplantation–specific Comorbidity Index (HCT-CI) were 61.7 and 65.7. In summary, a small set of comorbidities, aggregated into the SCI, is highly predictive of NRM. The new index stratifies patients into distinct risk groups, was validated in an external cohort, and provides higher discrimination than does the HCT-CI.
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spelling pubmed-89056942022-03-09 The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT Shouval, Roni Fein, Joshua A. Cho, Christina Avecilla, Scott T. Ruiz, Josel Tomas, Ana Alarcon Sanchez-Escamilla, Miriam Flores, Nerea Castillo Yáñez, Lucrecia Barker, Juliet N. Dahi, Parastoo Giralt, Sergio A. Geyer, Alexander I. Gyurkocza, Boglarka Jakubowski, Ann A. Lin, Richard J. O’Reilly, Richard J. Papadopoulos, Esperanza B. Politikos, Ioannis Ponce, Doris M. Sauter, Craig S. Scordo, Michael Shaffer, Brian Shah, Gunjan L. Sullivan, James P. Tamari, Roni van den Brink, Marcel R. M. Young, James W. Nagler, Arnon Devlin, Sean Shimoni, Avichai Perales, Miguel-Angel Blood Adv Transplantation Individual comorbidities have distinct contributions to nonrelapse mortality (NRM) following allogeneic hematopoietic cell transplantation (allo-HCT). We studied the impact of comorbidities individually and in combination in a single-center cohort of 573 adult patients who underwent CD34-selected allo-HCT following myeloablative conditioning. Pulmonary disease, moderate to severe hepatic comorbidity, cardiac disease of any type, and renal dysfunction were associated with increased NRM in multivariable Cox regression models. A Simplified Comorbidity Index (SCI) composed of the 4 comorbidities predictive of NRM, as well as age >60 years, stratified patients into 5 groups with a stepwise increase in NRM. NRM rates ranged from 11.4% to 49.9% by stratum, with adjusted hazard ratios of 1.84, 2.59, 3.57, and 5.38. The SCI was also applicable in an external cohort of 230 patients who underwent allo-HCT with unmanipulated grafts following intermediate-intensity conditioning. The area under the receiver operating characteristic curve (AUC) of the SCI for 1-year NRM was 70.3 and 72.0 over the development and external-validation cohorts, respectively; corresponding AUCs of the Hematopoietic Cell Transplantation–specific Comorbidity Index (HCT-CI) were 61.7 and 65.7. In summary, a small set of comorbidities, aggregated into the SCI, is highly predictive of NRM. The new index stratifies patients into distinct risk groups, was validated in an external cohort, and provides higher discrimination than does the HCT-CI. American Society of Hematology 2022-03-03 /pmc/articles/PMC8905694/ /pubmed/34507354 http://dx.doi.org/10.1182/bloodadvances.2021004319 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
spellingShingle Transplantation
Shouval, Roni
Fein, Joshua A.
Cho, Christina
Avecilla, Scott T.
Ruiz, Josel
Tomas, Ana Alarcon
Sanchez-Escamilla, Miriam
Flores, Nerea Castillo
Yáñez, Lucrecia
Barker, Juliet N.
Dahi, Parastoo
Giralt, Sergio A.
Geyer, Alexander I.
Gyurkocza, Boglarka
Jakubowski, Ann A.
Lin, Richard J.
O’Reilly, Richard J.
Papadopoulos, Esperanza B.
Politikos, Ioannis
Ponce, Doris M.
Sauter, Craig S.
Scordo, Michael
Shaffer, Brian
Shah, Gunjan L.
Sullivan, James P.
Tamari, Roni
van den Brink, Marcel R. M.
Young, James W.
Nagler, Arnon
Devlin, Sean
Shimoni, Avichai
Perales, Miguel-Angel
The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT
title The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT
title_full The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT
title_fullStr The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT
title_full_unstemmed The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT
title_short The Simplified Comorbidity Index: a new tool for prediction of nonrelapse mortality in allo-HCT
title_sort simplified comorbidity index: a new tool for prediction of nonrelapse mortality in allo-hct
topic Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905694/
https://www.ncbi.nlm.nih.gov/pubmed/34507354
http://dx.doi.org/10.1182/bloodadvances.2021004319
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