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Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis
One of the major challenges in rheumatology is to overcome the classification criteria that previously defined systemic lupus erythematosis, since the heterogeneity of the disease(s) appears to represent a complexity that probably substantially contributed to the failure of a number of recent trials...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003542/ https://www.ncbi.nlm.nih.gov/pubmed/19939293 http://dx.doi.org/10.1186/ar2834 |
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author | Smith, Michael F Hiepe, Falk Dörner, Thomas Burmester, Gerd |
author_facet | Smith, Michael F Hiepe, Falk Dörner, Thomas Burmester, Gerd |
author_sort | Smith, Michael F |
collection | PubMed |
description | One of the major challenges in rheumatology is to overcome the classification criteria that previously defined systemic lupus erythematosis, since the heterogeneity of the disease(s) appears to represent a complexity that probably substantially contributed to the failure of a number of recent trials. For those engaged in clinical trials, validated disease activity biomarkers that respond rapidly to treatment and are predictive of clinical response would greatly facilitate early decision-making around futility and dose selection. Likewise, use of validated patient stratification biomarkers possibly in conjunction with autoantibody profiles and disease manifestations will result in the recruitment of more homogeneous patient populations during later stage clinical studies, thereby decreasing size, costs, and risks in pivotal studies. |
format | Text |
id | pubmed-3003542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30035422010-12-18 Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis Smith, Michael F Hiepe, Falk Dörner, Thomas Burmester, Gerd Arthritis Res Ther Review One of the major challenges in rheumatology is to overcome the classification criteria that previously defined systemic lupus erythematosis, since the heterogeneity of the disease(s) appears to represent a complexity that probably substantially contributed to the failure of a number of recent trials. For those engaged in clinical trials, validated disease activity biomarkers that respond rapidly to treatment and are predictive of clinical response would greatly facilitate early decision-making around futility and dose selection. Likewise, use of validated patient stratification biomarkers possibly in conjunction with autoantibody profiles and disease manifestations will result in the recruitment of more homogeneous patient populations during later stage clinical studies, thereby decreasing size, costs, and risks in pivotal studies. BioMed Central 2009 2009-11-19 /pmc/articles/PMC3003542/ /pubmed/19939293 http://dx.doi.org/10.1186/ar2834 Text en Copyright ©2009 BioMed Central Ltd |
spellingShingle | Review Smith, Michael F Hiepe, Falk Dörner, Thomas Burmester, Gerd Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis |
title | Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis |
title_full | Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis |
title_fullStr | Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis |
title_full_unstemmed | Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis |
title_short | Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis |
title_sort | biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003542/ https://www.ncbi.nlm.nih.gov/pubmed/19939293 http://dx.doi.org/10.1186/ar2834 |
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