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Efficacy Endpoints in Clinical Trials in Actinic Keratosis
INTRODUCTION: Actinic keratosis is regarded as a chronic disease of the skin and, although fluctuating, is chronically progressive. Approval of new products for the treatment of actinic keratosis requires the use of a standard methodology in clinical trials which emphasize complete clearance of all...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109027/ https://www.ncbi.nlm.nih.gov/pubmed/29916197 http://dx.doi.org/10.1007/s13555-018-0247-0 |
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author | Skov, Torsten Stockfleth, Eggert Szeimies, Rolf-Markus Berman, Brian |
author_facet | Skov, Torsten Stockfleth, Eggert Szeimies, Rolf-Markus Berman, Brian |
author_sort | Skov, Torsten |
collection | PubMed |
description | INTRODUCTION: Actinic keratosis is regarded as a chronic disease of the skin and, although fluctuating, is chronically progressive. Approval of new products for the treatment of actinic keratosis requires the use of a standard methodology in clinical trials which emphasize complete clearance of all actinic keratoses in a treatment field in a defined time span and the evaluation of long-term efficacy in terms of recurrence rate among completely cleared patients. METHODS: Analysis of data from six previously published clinical trials in patients with actinic keratosis. RESULTS: There was poor agreement over a period of 1 month in the complete clearance endpoint. This variation in assessment renders recurrence in cleared patients invalid as the estimate of long-term efficacy. Furthermore, complete clearance was shown to depend heavily on the number of baseline actinic keratoses. CONCLUSION: The main endpoints presently in use for the assessment of short- and long-term efficacy of actinic keratosis field-directed therapy, namely, complete clearance and recurrence rate, are obsolete and should be replaced by the percentage reduction in actinic keratosis count or the absolute actinic keratosis count. FUNDING: LEO Pharma A/S. |
format | Online Article Text |
id | pubmed-6109027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-61090272018-08-31 Efficacy Endpoints in Clinical Trials in Actinic Keratosis Skov, Torsten Stockfleth, Eggert Szeimies, Rolf-Markus Berman, Brian Dermatol Ther (Heidelb) Original Research INTRODUCTION: Actinic keratosis is regarded as a chronic disease of the skin and, although fluctuating, is chronically progressive. Approval of new products for the treatment of actinic keratosis requires the use of a standard methodology in clinical trials which emphasize complete clearance of all actinic keratoses in a treatment field in a defined time span and the evaluation of long-term efficacy in terms of recurrence rate among completely cleared patients. METHODS: Analysis of data from six previously published clinical trials in patients with actinic keratosis. RESULTS: There was poor agreement over a period of 1 month in the complete clearance endpoint. This variation in assessment renders recurrence in cleared patients invalid as the estimate of long-term efficacy. Furthermore, complete clearance was shown to depend heavily on the number of baseline actinic keratoses. CONCLUSION: The main endpoints presently in use for the assessment of short- and long-term efficacy of actinic keratosis field-directed therapy, namely, complete clearance and recurrence rate, are obsolete and should be replaced by the percentage reduction in actinic keratosis count or the absolute actinic keratosis count. FUNDING: LEO Pharma A/S. Springer Healthcare 2018-06-18 /pmc/articles/PMC6109027/ /pubmed/29916197 http://dx.doi.org/10.1007/s13555-018-0247-0 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Skov, Torsten Stockfleth, Eggert Szeimies, Rolf-Markus Berman, Brian Efficacy Endpoints in Clinical Trials in Actinic Keratosis |
title | Efficacy Endpoints in Clinical Trials in Actinic Keratosis |
title_full | Efficacy Endpoints in Clinical Trials in Actinic Keratosis |
title_fullStr | Efficacy Endpoints in Clinical Trials in Actinic Keratosis |
title_full_unstemmed | Efficacy Endpoints in Clinical Trials in Actinic Keratosis |
title_short | Efficacy Endpoints in Clinical Trials in Actinic Keratosis |
title_sort | efficacy endpoints in clinical trials in actinic keratosis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109027/ https://www.ncbi.nlm.nih.gov/pubmed/29916197 http://dx.doi.org/10.1007/s13555-018-0247-0 |
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