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Validation of Minnesota acute graft-versus-host disease Risk Score

Using multicenter data, we developed a novel acute graft-versus-host disease Risk Score which more accurately predicts response to steroid treatment, survival and transplant related mortality than other published risk scores based upon clinical grading criteria.(1) To validate this Risk Score in a c...

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Autores principales: MacMillan, Margaret L., DeFor, Todd E., Holtan, Shernan G., Rashidi, Armin, Blazar, Bruce R., Weisdorf, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012472/
https://www.ncbi.nlm.nih.gov/pubmed/31320554
http://dx.doi.org/10.3324/haematol.2019.220970
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author MacMillan, Margaret L.
DeFor, Todd E.
Holtan, Shernan G.
Rashidi, Armin
Blazar, Bruce R.
Weisdorf, Daniel J.
author_facet MacMillan, Margaret L.
DeFor, Todd E.
Holtan, Shernan G.
Rashidi, Armin
Blazar, Bruce R.
Weisdorf, Daniel J.
author_sort MacMillan, Margaret L.
collection PubMed
description Using multicenter data, we developed a novel acute graft-versus-host disease Risk Score which more accurately predicts response to steroid treatment, survival and transplant related mortality than other published risk scores based upon clinical grading criteria.(1) To validate this Risk Score in a contemporary cohort, we examined 355 recent University of Minnesota patients (2007-2016) diagnosed with acute graft-versus-host disease and treated with prednisone 60 mg/m(2)/day for 14 days, followed by an 8-week taper. Overall response [complete response + partial response] was higher in the 276 standard risk versus 79 high risk graft-versus-host disease patients at day 14 (71% versus 56%, P<0.01), day 28 (74% versus 59%, P=0.02) and day 56 (68% versus 49%, P<0.01) after steroid initiation. Day 28 response did not differ by the initial graft-versus-host disease grade. In multiple regression analysis, patients with high risk graft-versus-host disease were less likely to respond at day 28 (odds ratio 0.5, 95% CI 0.3-0.9, P<0.01) and had higher risks of 2 year transplant related mortality (Hazard Ratio 1.8, 95% CI, 1.0-2.1, P=0.03) and overall mortality (Hazard Ratio 1.7, 95% CI, 1.2-2.4, P<0.01) than patients with a standard risk graft-versus-host disease. This analysis confirms the Minnesota graft-versus-host disease Risk Score as a valuable bedside tool to define risk in patients with acute graft-versus-host disease. A tailored approach to upfront acute graft-versus-host disease therapy based upon the Minnesota Risk Score may improve outcomes and facilitate testing of novel treatments in these patients.
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spelling pubmed-70124722020-02-20 Validation of Minnesota acute graft-versus-host disease Risk Score MacMillan, Margaret L. DeFor, Todd E. Holtan, Shernan G. Rashidi, Armin Blazar, Bruce R. Weisdorf, Daniel J. Haematologica Article Using multicenter data, we developed a novel acute graft-versus-host disease Risk Score which more accurately predicts response to steroid treatment, survival and transplant related mortality than other published risk scores based upon clinical grading criteria.(1) To validate this Risk Score in a contemporary cohort, we examined 355 recent University of Minnesota patients (2007-2016) diagnosed with acute graft-versus-host disease and treated with prednisone 60 mg/m(2)/day for 14 days, followed by an 8-week taper. Overall response [complete response + partial response] was higher in the 276 standard risk versus 79 high risk graft-versus-host disease patients at day 14 (71% versus 56%, P<0.01), day 28 (74% versus 59%, P=0.02) and day 56 (68% versus 49%, P<0.01) after steroid initiation. Day 28 response did not differ by the initial graft-versus-host disease grade. In multiple regression analysis, patients with high risk graft-versus-host disease were less likely to respond at day 28 (odds ratio 0.5, 95% CI 0.3-0.9, P<0.01) and had higher risks of 2 year transplant related mortality (Hazard Ratio 1.8, 95% CI, 1.0-2.1, P=0.03) and overall mortality (Hazard Ratio 1.7, 95% CI, 1.2-2.4, P<0.01) than patients with a standard risk graft-versus-host disease. This analysis confirms the Minnesota graft-versus-host disease Risk Score as a valuable bedside tool to define risk in patients with acute graft-versus-host disease. A tailored approach to upfront acute graft-versus-host disease therapy based upon the Minnesota Risk Score may improve outcomes and facilitate testing of novel treatments in these patients. Ferrata Storti Foundation 2020-02 /pmc/articles/PMC7012472/ /pubmed/31320554 http://dx.doi.org/10.3324/haematol.2019.220970 Text en Copyright© 2020 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Article
MacMillan, Margaret L.
DeFor, Todd E.
Holtan, Shernan G.
Rashidi, Armin
Blazar, Bruce R.
Weisdorf, Daniel J.
Validation of Minnesota acute graft-versus-host disease Risk Score
title Validation of Minnesota acute graft-versus-host disease Risk Score
title_full Validation of Minnesota acute graft-versus-host disease Risk Score
title_fullStr Validation of Minnesota acute graft-versus-host disease Risk Score
title_full_unstemmed Validation of Minnesota acute graft-versus-host disease Risk Score
title_short Validation of Minnesota acute graft-versus-host disease Risk Score
title_sort validation of minnesota acute graft-versus-host disease risk score
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012472/
https://www.ncbi.nlm.nih.gov/pubmed/31320554
http://dx.doi.org/10.3324/haematol.2019.220970
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