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Use of Lesion Response Rate in Actinic Keratosis Trials

Complete patient clearance is often required by regulatory agencies for the approval of treatments for actinic keratosis (AK). However, an increasing number of clinicians have challenged the use of this measure in clinical practice and its interpretation. It has been argued that complete patient cle...

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Autores principales: Szeimies, Rolf-Markus, Atanasov, Petar, Bissonnette, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120634/
https://www.ncbi.nlm.nih.gov/pubmed/27645828
http://dx.doi.org/10.1007/s13555-016-0145-2
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author Szeimies, Rolf-Markus
Atanasov, Petar
Bissonnette, Robert
author_facet Szeimies, Rolf-Markus
Atanasov, Petar
Bissonnette, Robert
author_sort Szeimies, Rolf-Markus
collection PubMed
description Complete patient clearance is often required by regulatory agencies for the approval of treatments for actinic keratosis (AK). However, an increasing number of clinicians have challenged the use of this measure in clinical practice and its interpretation. It has been argued that complete patient clearance often underestimates the clinical benefit of a drug and is influenced by a number of key confounding factors, such as number and distribution of lesions, at baseline. Lesions response rate is one alternative which has been suggested as more relevant due to its applicability to clinical practice and closer reflection of the clinical value of the drug. This paper provides an updated perspective on the topic and details the current thinking on the role of complete clearance and lesion response rate in the context of AK. Funding: Galderma.
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spelling pubmed-51206342016-12-07 Use of Lesion Response Rate in Actinic Keratosis Trials Szeimies, Rolf-Markus Atanasov, Petar Bissonnette, Robert Dermatol Ther (Heidelb) Commentary Complete patient clearance is often required by regulatory agencies for the approval of treatments for actinic keratosis (AK). However, an increasing number of clinicians have challenged the use of this measure in clinical practice and its interpretation. It has been argued that complete patient clearance often underestimates the clinical benefit of a drug and is influenced by a number of key confounding factors, such as number and distribution of lesions, at baseline. Lesions response rate is one alternative which has been suggested as more relevant due to its applicability to clinical practice and closer reflection of the clinical value of the drug. This paper provides an updated perspective on the topic and details the current thinking on the role of complete clearance and lesion response rate in the context of AK. Funding: Galderma. Springer Healthcare 2016-09-19 /pmc/articles/PMC5120634/ /pubmed/27645828 http://dx.doi.org/10.1007/s13555-016-0145-2 Text en © The Author(s) 2016 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 Commentary
Szeimies, Rolf-Markus
Atanasov, Petar
Bissonnette, Robert
Use of Lesion Response Rate in Actinic Keratosis Trials
title Use of Lesion Response Rate in Actinic Keratosis Trials
title_full Use of Lesion Response Rate in Actinic Keratosis Trials
title_fullStr Use of Lesion Response Rate in Actinic Keratosis Trials
title_full_unstemmed Use of Lesion Response Rate in Actinic Keratosis Trials
title_short Use of Lesion Response Rate in Actinic Keratosis Trials
title_sort use of lesion response rate in actinic keratosis trials
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120634/
https://www.ncbi.nlm.nih.gov/pubmed/27645828
http://dx.doi.org/10.1007/s13555-016-0145-2
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