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Protein C as a surrogate end-point for clinical trials of sepsis
Identification of good surrogate end-points can greatly facilitate the design of clinical trials. Using data from PROWESS and ENHANCE, Shorr and colleagues explore the potential value of several plasma biomarkers for treatment trials of activated protein C for severe sepsis. Based on the framework p...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447596/ https://www.ncbi.nlm.nih.gov/pubmed/18492215 http://dx.doi.org/10.1186/cc6859 |
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author | Liu, Kathleen D Matthay, Michael A |
author_facet | Liu, Kathleen D Matthay, Michael A |
author_sort | Liu, Kathleen D |
collection | PubMed |
description | Identification of good surrogate end-points can greatly facilitate the design of clinical trials. Using data from PROWESS and ENHANCE, Shorr and colleagues explore the potential value of several plasma biomarkers for treatment trials of activated protein C for severe sepsis. Based on the framework proposed by Vasan, they tested the utility of several factors (protein C, interleukin-6, antithrombin III, prothrombin time, protein S, and d-dimers) as type 0, 1 and 2 biomarkers. Only protein C had acceptable performance characteristics as a type 2 biomarker, or surrogate end-point. The utility of protein C as a surrogate end-point for studies of severe sepsis must be validated in future prospective studies. |
format | Text |
id | pubmed-2447596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24475962008-07-10 Protein C as a surrogate end-point for clinical trials of sepsis Liu, Kathleen D Matthay, Michael A Crit Care Commentary Identification of good surrogate end-points can greatly facilitate the design of clinical trials. Using data from PROWESS and ENHANCE, Shorr and colleagues explore the potential value of several plasma biomarkers for treatment trials of activated protein C for severe sepsis. Based on the framework proposed by Vasan, they tested the utility of several factors (protein C, interleukin-6, antithrombin III, prothrombin time, protein S, and d-dimers) as type 0, 1 and 2 biomarkers. Only protein C had acceptable performance characteristics as a type 2 biomarker, or surrogate end-point. The utility of protein C as a surrogate end-point for studies of severe sepsis must be validated in future prospective studies. BioMed Central 2008 2008-04-24 /pmc/articles/PMC2447596/ /pubmed/18492215 http://dx.doi.org/10.1186/cc6859 Text en Copyright © 2008 BioMed Central Ltd |
spellingShingle | Commentary Liu, Kathleen D Matthay, Michael A Protein C as a surrogate end-point for clinical trials of sepsis |
title | Protein C as a surrogate end-point for clinical trials of sepsis |
title_full | Protein C as a surrogate end-point for clinical trials of sepsis |
title_fullStr | Protein C as a surrogate end-point for clinical trials of sepsis |
title_full_unstemmed | Protein C as a surrogate end-point for clinical trials of sepsis |
title_short | Protein C as a surrogate end-point for clinical trials of sepsis |
title_sort | protein c as a surrogate end-point for clinical trials of sepsis |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447596/ https://www.ncbi.nlm.nih.gov/pubmed/18492215 http://dx.doi.org/10.1186/cc6859 |
work_keys_str_mv | AT liukathleend proteincasasurrogateendpointforclinicaltrialsofsepsis AT matthaymichaela proteincasasurrogateendpointforclinicaltrialsofsepsis |