Phenol peels as a novel therapeutic approach for actinic keratosis and Bowen disease: Prospective pilot trial with assessment of clinical, histologic, and immunohistochemical correlations

Background Although chemical peels may be used for precancerous lesions, no histologic or immunohistochemical studies have been performed to validate clinical impressions and/or outcome. Objective Our purpose was to investigate the efficacy and prognostic relevance of phenol peels in Japanese patien...

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Veröffentlicht in:Journal of the American Academy of Dermatology 2009-04, Vol.60 (4), p.615-625
Hauptverfasser: Kaminaka, Chikako, MD, Yamamoto, Yuki, MD, PhD, Yonei, Nozomi, MD, PhD, Kishioka, Akiko, MD, Kondo, Toshikazu, MD, PhD, Furukawa, Fukumi, MD, PhD
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container_end_page 625
container_issue 4
container_start_page 615
container_title Journal of the American Academy of Dermatology
container_volume 60
creator Kaminaka, Chikako, MD
Yamamoto, Yuki, MD, PhD
Yonei, Nozomi, MD, PhD
Kishioka, Akiko, MD
Kondo, Toshikazu, MD, PhD
Furukawa, Fukumi, MD, PhD
description Background Although chemical peels may be used for precancerous lesions, no histologic or immunohistochemical studies have been performed to validate clinical impressions and/or outcome. Objective Our purpose was to investigate the efficacy and prognostic relevance of phenol peels in Japanese patients with actinic keratosis and Bowen disease using clinical and histologic criteria. Methods A total of 46 patients were treated with phenol peels, and followed up for at least 1 year after treatment. Biopsy specimens were taken before and after treatment. Cases of complete response were classified by the number of treatment sessions. We evaluated parameters for epidermal thickness, proliferation, dysplasia, and apoptosis, and clinical characteristics to correlate phenol peels with assessments of efficacy, patient-selection criteria, and risk for transformation to cutaneous squamous cell carcinoma. Results There were 39 (84.8%) patients with a complete response after one to 8 treatment sessions. Statistically, differences in clinical improvement with peels and the number of treatment sessions correlated with histology, personal history of skin cancer, tumor thickness, and cyclin A expression. Limitations This study was a prospective pilot trial. Blinded, placebo-controlled, randomized studies would be ideal. Conclusion We conclude that phenol peels are very effective for treating precancerous lesions of actinic keratosis and Bowen disease. In addition, our study clearly demonstrates that tumor thickness and cyclin A could be specific and useful markers as adjunctive diagnostic tools to predict the efficacy of phenol treatment of these lesions.
doi_str_mv 10.1016/j.jaad.2008.11.907
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Objective Our purpose was to investigate the efficacy and prognostic relevance of phenol peels in Japanese patients with actinic keratosis and Bowen disease using clinical and histologic criteria. Methods A total of 46 patients were treated with phenol peels, and followed up for at least 1 year after treatment. Biopsy specimens were taken before and after treatment. Cases of complete response were classified by the number of treatment sessions. We evaluated parameters for epidermal thickness, proliferation, dysplasia, and apoptosis, and clinical characteristics to correlate phenol peels with assessments of efficacy, patient-selection criteria, and risk for transformation to cutaneous squamous cell carcinoma. Results There were 39 (84.8%) patients with a complete response after one to 8 treatment sessions. Statistically, differences in clinical improvement with peels and the number of treatment sessions correlated with histology, personal history of skin cancer, tumor thickness, and cyclin A expression. Limitations This study was a prospective pilot trial. Blinded, placebo-controlled, randomized studies would be ideal. Conclusion We conclude that phenol peels are very effective for treating precancerous lesions of actinic keratosis and Bowen disease. In addition, our study clearly demonstrates that tumor thickness and cyclin A could be specific and useful markers as adjunctive diagnostic tools to predict the efficacy of phenol treatment of these lesions.</description><identifier>ISSN: 0190-9622</identifier><identifier>EISSN: 1097-6787</identifier><identifier>DOI: 10.1016/j.jaad.2008.11.907</identifier><identifier>PMID: 19293009</identifier><identifier>CODEN: JAADDB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>actinic keratosis ; Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Bowen disease ; Bowen's Disease - drug therapy ; cyclin A ; Dermatology ; Dyskeratosis ; Female ; Humans ; Keratolytic Agents - therapeutic use ; Keratosis, Actinic - drug therapy ; Male ; Medical sciences ; Middle Aged ; phenol ; Phenols - therapeutic use ; Pilot Projects ; Prospective Studies ; squamous cell carcinoma ; treatment ; tumor thickness ; Tumors of the skin and soft tissue. 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Objective Our purpose was to investigate the efficacy and prognostic relevance of phenol peels in Japanese patients with actinic keratosis and Bowen disease using clinical and histologic criteria. Methods A total of 46 patients were treated with phenol peels, and followed up for at least 1 year after treatment. Biopsy specimens were taken before and after treatment. Cases of complete response were classified by the number of treatment sessions. We evaluated parameters for epidermal thickness, proliferation, dysplasia, and apoptosis, and clinical characteristics to correlate phenol peels with assessments of efficacy, patient-selection criteria, and risk for transformation to cutaneous squamous cell carcinoma. Results There were 39 (84.8%) patients with a complete response after one to 8 treatment sessions. Statistically, differences in clinical improvement with peels and the number of treatment sessions correlated with histology, personal history of skin cancer, tumor thickness, and cyclin A expression. Limitations This study was a prospective pilot trial. Blinded, placebo-controlled, randomized studies would be ideal. Conclusion We conclude that phenol peels are very effective for treating precancerous lesions of actinic keratosis and Bowen disease. In addition, our study clearly demonstrates that tumor thickness and cyclin A could be specific and useful markers as adjunctive diagnostic tools to predict the efficacy of phenol treatment of these lesions.</description><subject>actinic keratosis</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Bowen disease</subject><subject>Bowen's Disease - drug therapy</subject><subject>cyclin A</subject><subject>Dermatology</subject><subject>Dyskeratosis</subject><subject>Female</subject><subject>Humans</subject><subject>Keratolytic Agents - therapeutic use</subject><subject>Keratosis, Actinic - drug therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>phenol</subject><subject>Phenols - therapeutic use</subject><subject>Pilot Projects</subject><subject>Prospective Studies</subject><subject>squamous cell carcinoma</subject><subject>treatment</subject><subject>tumor thickness</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0190-9622</issn><issn>1097-6787</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kt-O1CAUxhujccfVF_DCcKNXOyNQWooxJrrxX7KJm6jXhKEHyyyFLtDZ7LP5ctKdURMvTEgIh-_7gPOjqp4SvCGYtC93m51S_YZi3G0I2QjM71UrggVft7zj96sVJgKvRUvpSfUopR3GWLCaP6xOiKCiLqtV9fNyAB8cmgBcQqoM5MMeHMoDRDXBnK1GappiUHpAJkSkdLa-FK_Kfg7JFovv0btwAx71NoFK8ApdxpAmKMo9oMm6kFGOVjl0Y_NQTkmQ0gg-o2CQdkuccmdosCkHF35YfXaXacdx9uGuqgcYFxHSIUZwKtvg0-PqgVEuwZPjfFp9__D-2_mn9cWXj5_P316sNatFXndsy7RqtspogzUxuuVcKINh2_K6MRwL0W8VEUCUaTU01DCmO6JFaxhntalPqxeH3NKF6xlSlqNNGpxTHsKcZMsx6yilRUgPQl2enyIYOUU7qngrCZYLMrmTCzK5IJOEyIKsmJ4d0-ftCP1fy5FRETw_ClQqLTBReW3THx0ltGuabgl6fdAVkrC3EGXSFryG3saCQvbB_v8eb_6x_yZzBbeQdmGOvnRZEpmoxPLr8rmWv4U7TFnHmvoXaSfPkQ</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Kaminaka, Chikako, MD</creator><creator>Yamamoto, Yuki, MD, PhD</creator><creator>Yonei, Nozomi, MD, PhD</creator><creator>Kishioka, Akiko, MD</creator><creator>Kondo, Toshikazu, MD, PhD</creator><creator>Furukawa, Fukumi, MD, PhD</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090401</creationdate><title>Phenol peels as a novel therapeutic approach for actinic keratosis and Bowen disease: Prospective pilot trial with assessment of clinical, histologic, and immunohistochemical correlations</title><author>Kaminaka, Chikako, MD ; Yamamoto, Yuki, MD, PhD ; Yonei, Nozomi, MD, PhD ; Kishioka, Akiko, MD ; Kondo, Toshikazu, MD, PhD ; Furukawa, Fukumi, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-84b4ca5bafcf0c1fc6779af0eb6735f7099dba19e1af6ce52f44c81c96f4743f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>actinic keratosis</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Bowen disease</topic><topic>Bowen's Disease - drug therapy</topic><topic>cyclin A</topic><topic>Dermatology</topic><topic>Dyskeratosis</topic><topic>Female</topic><topic>Humans</topic><topic>Keratolytic Agents - therapeutic use</topic><topic>Keratosis, Actinic - drug therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>phenol</topic><topic>Phenols - therapeutic use</topic><topic>Pilot Projects</topic><topic>Prospective Studies</topic><topic>squamous cell carcinoma</topic><topic>treatment</topic><topic>tumor thickness</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaminaka, Chikako, MD</creatorcontrib><creatorcontrib>Yamamoto, Yuki, MD, PhD</creatorcontrib><creatorcontrib>Yonei, Nozomi, MD, PhD</creatorcontrib><creatorcontrib>Kishioka, Akiko, MD</creatorcontrib><creatorcontrib>Kondo, Toshikazu, MD, PhD</creatorcontrib><creatorcontrib>Furukawa, Fukumi, MD, PhD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Academy of Dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaminaka, Chikako, MD</au><au>Yamamoto, Yuki, MD, PhD</au><au>Yonei, Nozomi, MD, PhD</au><au>Kishioka, Akiko, MD</au><au>Kondo, Toshikazu, MD, PhD</au><au>Furukawa, Fukumi, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenol peels as a novel therapeutic approach for actinic keratosis and Bowen disease: Prospective pilot trial with assessment of clinical, histologic, and immunohistochemical correlations</atitle><jtitle>Journal of the American Academy of Dermatology</jtitle><addtitle>J Am Acad Dermatol</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>60</volume><issue>4</issue><spage>615</spage><epage>625</epage><pages>615-625</pages><issn>0190-9622</issn><eissn>1097-6787</eissn><coden>JAADDB</coden><abstract>Background Although chemical peels may be used for precancerous lesions, no histologic or immunohistochemical studies have been performed to validate clinical impressions and/or outcome. Objective Our purpose was to investigate the efficacy and prognostic relevance of phenol peels in Japanese patients with actinic keratosis and Bowen disease using clinical and histologic criteria. Methods A total of 46 patients were treated with phenol peels, and followed up for at least 1 year after treatment. Biopsy specimens were taken before and after treatment. Cases of complete response were classified by the number of treatment sessions. We evaluated parameters for epidermal thickness, proliferation, dysplasia, and apoptosis, and clinical characteristics to correlate phenol peels with assessments of efficacy, patient-selection criteria, and risk for transformation to cutaneous squamous cell carcinoma. Results There were 39 (84.8%) patients with a complete response after one to 8 treatment sessions. Statistically, differences in clinical improvement with peels and the number of treatment sessions correlated with histology, personal history of skin cancer, tumor thickness, and cyclin A expression. Limitations This study was a prospective pilot trial. Blinded, placebo-controlled, randomized studies would be ideal. Conclusion We conclude that phenol peels are very effective for treating precancerous lesions of actinic keratosis and Bowen disease. In addition, our study clearly demonstrates that tumor thickness and cyclin A could be specific and useful markers as adjunctive diagnostic tools to predict the efficacy of phenol treatment of these lesions.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>19293009</pmid><doi>10.1016/j.jaad.2008.11.907</doi><tpages>11</tpages></addata></record>
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subjects actinic keratosis
Adult
Aged
Aged, 80 and over
Biological and medical sciences
Bowen disease
Bowen's Disease - drug therapy
cyclin A
Dermatology
Dyskeratosis
Female
Humans
Keratolytic Agents - therapeutic use
Keratosis, Actinic - drug therapy
Male
Medical sciences
Middle Aged
phenol
Phenols - therapeutic use
Pilot Projects
Prospective Studies
squamous cell carcinoma
treatment
tumor thickness
Tumors of the skin and soft tissue. Premalignant lesions
title Phenol peels as a novel therapeutic approach for actinic keratosis and Bowen disease: Prospective pilot trial with assessment of clinical, histologic, and immunohistochemical correlations
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