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In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy

SIMPLE SUMMARY: The assessment of actinic keratoses (AKs) in prevention and therapeutic trials, as well as clinical practice, could significantly benefit from the incorporation of non-invasive imaging technology. Such technology has the potential to enhance the objective evaluation of clinical and s...

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Autores principales: Curiel-Lewandrowski, Clara, Myrdal, Caitlyn N., Saboda, Kathylynn, Hu, Chengcheng, Arzberger, Edith, Pellacani, Giovanni, Legat, Franz Josef, Ulrich, Martina, Hochfellner, Petra, Oliviero, Margaret C., Pasquali, Paola, Gill, Melissa, Hofmann-Wellenhof, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8583298/
https://www.ncbi.nlm.nih.gov/pubmed/34771651
http://dx.doi.org/10.3390/cancers13215488
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author Curiel-Lewandrowski, Clara
Myrdal, Caitlyn N.
Saboda, Kathylynn
Hu, Chengcheng
Arzberger, Edith
Pellacani, Giovanni
Legat, Franz Josef
Ulrich, Martina
Hochfellner, Petra
Oliviero, Margaret C.
Pasquali, Paola
Gill, Melissa
Hofmann-Wellenhof, Rainer
author_facet Curiel-Lewandrowski, Clara
Myrdal, Caitlyn N.
Saboda, Kathylynn
Hu, Chengcheng
Arzberger, Edith
Pellacani, Giovanni
Legat, Franz Josef
Ulrich, Martina
Hochfellner, Petra
Oliviero, Margaret C.
Pasquali, Paola
Gill, Melissa
Hofmann-Wellenhof, Rainer
author_sort Curiel-Lewandrowski, Clara
collection PubMed
description SIMPLE SUMMARY: The assessment of actinic keratoses (AKs) in prevention and therapeutic trials, as well as clinical practice, could significantly benefit from the incorporation of non-invasive imaging technology. Such technology has the potential to enhance the objective evaluation of clinical and subclinical AKs with the added advantage of sequential monitoring. In vivo reflectance confocal microscopy (RCM) allows for the non-invasive imaging of AKs at a cellular level. We aimed to establish an in in vivo RCM protocol for AK response monitoring, ultimately leading to more reliable characterization of longitudinal responses and therapy optimization. ABSTRACT: Reflectance confocal microscopy (RCM) presents a non-invasive method to image actinic keratosis (AK) at a cellular level. However, RCM criteria for AK response monitoring vary across studies and a universal, standardized approach is lacking. We aimed to identify reliable AK response criteria and to compare the clinical and RCM evaluation of responses across AK severity grades. Twenty patients were included and randomized to receive either cryotherapy (n = 10) or PDT (n = 10). Clinical assessment and RCM evaluation of 12 criteria were performed in AK lesions and photodamaged skin at baseline, 3 and 6 months. We identified the RCM criteria that reliably characterize AK at baseline and display significant reduction following treatment. Those with the highest baseline odds ratio (OR), good interobserver agreement, and most significant change over time were atypical honeycomb pattern (OR: 12.7, CI: 5.7–28.1), hyperkeratosis (OR: 13.6, CI: 5.3–34.9), stratum corneum disruption (OR: 7.8, CI: 3.5–17.3), and disarranged epidermal pattern (OR: 6.5, CI: 2.9–14.8). Clinical evaluation demonstrated a significant treatment response without relapse. However, in grade 2 AK, 10/12 RCM parameters increased from 3 to 6 months, which suggested early subclinical recurrence detection by RCM. Incorporating standardized RCM protocols for the assessment of AK may enable a more meaningful comparison across clinical trials, while allowing for the early detection of relapses and evaluation of biological responses to therapy over time.
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spelling pubmed-85832982021-11-12 In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy Curiel-Lewandrowski, Clara Myrdal, Caitlyn N. Saboda, Kathylynn Hu, Chengcheng Arzberger, Edith Pellacani, Giovanni Legat, Franz Josef Ulrich, Martina Hochfellner, Petra Oliviero, Margaret C. Pasquali, Paola Gill, Melissa Hofmann-Wellenhof, Rainer Cancers (Basel) Article SIMPLE SUMMARY: The assessment of actinic keratoses (AKs) in prevention and therapeutic trials, as well as clinical practice, could significantly benefit from the incorporation of non-invasive imaging technology. Such technology has the potential to enhance the objective evaluation of clinical and subclinical AKs with the added advantage of sequential monitoring. In vivo reflectance confocal microscopy (RCM) allows for the non-invasive imaging of AKs at a cellular level. We aimed to establish an in in vivo RCM protocol for AK response monitoring, ultimately leading to more reliable characterization of longitudinal responses and therapy optimization. ABSTRACT: Reflectance confocal microscopy (RCM) presents a non-invasive method to image actinic keratosis (AK) at a cellular level. However, RCM criteria for AK response monitoring vary across studies and a universal, standardized approach is lacking. We aimed to identify reliable AK response criteria and to compare the clinical and RCM evaluation of responses across AK severity grades. Twenty patients were included and randomized to receive either cryotherapy (n = 10) or PDT (n = 10). Clinical assessment and RCM evaluation of 12 criteria were performed in AK lesions and photodamaged skin at baseline, 3 and 6 months. We identified the RCM criteria that reliably characterize AK at baseline and display significant reduction following treatment. Those with the highest baseline odds ratio (OR), good interobserver agreement, and most significant change over time were atypical honeycomb pattern (OR: 12.7, CI: 5.7–28.1), hyperkeratosis (OR: 13.6, CI: 5.3–34.9), stratum corneum disruption (OR: 7.8, CI: 3.5–17.3), and disarranged epidermal pattern (OR: 6.5, CI: 2.9–14.8). Clinical evaluation demonstrated a significant treatment response without relapse. However, in grade 2 AK, 10/12 RCM parameters increased from 3 to 6 months, which suggested early subclinical recurrence detection by RCM. Incorporating standardized RCM protocols for the assessment of AK may enable a more meaningful comparison across clinical trials, while allowing for the early detection of relapses and evaluation of biological responses to therapy over time. MDPI 2021-10-31 /pmc/articles/PMC8583298/ /pubmed/34771651 http://dx.doi.org/10.3390/cancers13215488 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Curiel-Lewandrowski, Clara
Myrdal, Caitlyn N.
Saboda, Kathylynn
Hu, Chengcheng
Arzberger, Edith
Pellacani, Giovanni
Legat, Franz Josef
Ulrich, Martina
Hochfellner, Petra
Oliviero, Margaret C.
Pasquali, Paola
Gill, Melissa
Hofmann-Wellenhof, Rainer
In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy
title In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy
title_full In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy
title_fullStr In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy
title_full_unstemmed In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy
title_short In Vivo Reflectance Confocal Microscopy as a Response Monitoring Tool for Actinic Keratoses Undergoing Cryotherapy and Photodynamic Therapy
title_sort in vivo reflectance confocal microscopy as a response monitoring tool for actinic keratoses undergoing cryotherapy and photodynamic therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8583298/
https://www.ncbi.nlm.nih.gov/pubmed/34771651
http://dx.doi.org/10.3390/cancers13215488
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