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A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients

BACKGROUND: Solid organ transplant recipients (SOTR) are at high risk of keratinocyte carcinoma (KC). Long‐term evidence for acitretin as chemoprophylaxis in this population is lacking. OBJECTIVE: To determine the benefit of long‐term acitretin for KC chemoprevention in SOTR. METHODS: A retrospectiv...

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Autores principales: Allnutt, Katherine J, Vogrin, Sara, Li, Jane, Goh, Michelle S, Brennand, Sarah, Davenport, Rachael, Chong, Alvin H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9311671/
https://www.ncbi.nlm.nih.gov/pubmed/35333399
http://dx.doi.org/10.1111/ajd.13821
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author Allnutt, Katherine J
Vogrin, Sara
Li, Jane
Goh, Michelle S
Brennand, Sarah
Davenport, Rachael
Chong, Alvin H
author_facet Allnutt, Katherine J
Vogrin, Sara
Li, Jane
Goh, Michelle S
Brennand, Sarah
Davenport, Rachael
Chong, Alvin H
author_sort Allnutt, Katherine J
collection PubMed
description BACKGROUND: Solid organ transplant recipients (SOTR) are at high risk of keratinocyte carcinoma (KC). Long‐term evidence for acitretin as chemoprophylaxis in this population is lacking. OBJECTIVE: To determine the benefit of long‐term acitretin for KC chemoprevention in SOTR. METHODS: A retrospective cohort study of SOTR treated with acitretin at an Australian transplant dermatology clinic was performed. General estimating equations were used to evaluate change in rates of histologically confirmed KC in the 6–12 months prior to acitretin and following a minimum 6 months of treatment. A control group of patients within the same service was included, comprising SOTR who were not treated with acitretin. RESULTS: Twenty‐two patients received acitretin treatment for at least 6 months, eighteen for at least 5 years and four for at least 9 years. The median KC rate pretreatment was 3.31 per year (IQR 1.93, 5.40). There was a significant reduction in the rate of KC in the first year of acitretin treatment (IRR 0.41, 95% CI 0.22, 0.76, P = 0.005), and this effect was observed for 5 years (IRR at 5 years 0.34, 95% CI 0.17, 0.67, P = 0.002). The control group had no statistically significant change in KC rate over time in the study. CONCLUSIONS: Acitretin appears to be well‐tolerated and effective in reducing KC in SOTR for at least 5 years. Study limitations include its retrospective nature, small sample size and lack of blinding.
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spelling pubmed-93116712022-07-29 A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients Allnutt, Katherine J Vogrin, Sara Li, Jane Goh, Michelle S Brennand, Sarah Davenport, Rachael Chong, Alvin H Australas J Dermatol Original Research BACKGROUND: Solid organ transplant recipients (SOTR) are at high risk of keratinocyte carcinoma (KC). Long‐term evidence for acitretin as chemoprophylaxis in this population is lacking. OBJECTIVE: To determine the benefit of long‐term acitretin for KC chemoprevention in SOTR. METHODS: A retrospective cohort study of SOTR treated with acitretin at an Australian transplant dermatology clinic was performed. General estimating equations were used to evaluate change in rates of histologically confirmed KC in the 6–12 months prior to acitretin and following a minimum 6 months of treatment. A control group of patients within the same service was included, comprising SOTR who were not treated with acitretin. RESULTS: Twenty‐two patients received acitretin treatment for at least 6 months, eighteen for at least 5 years and four for at least 9 years. The median KC rate pretreatment was 3.31 per year (IQR 1.93, 5.40). There was a significant reduction in the rate of KC in the first year of acitretin treatment (IRR 0.41, 95% CI 0.22, 0.76, P = 0.005), and this effect was observed for 5 years (IRR at 5 years 0.34, 95% CI 0.17, 0.67, P = 0.002). The control group had no statistically significant change in KC rate over time in the study. CONCLUSIONS: Acitretin appears to be well‐tolerated and effective in reducing KC in SOTR for at least 5 years. Study limitations include its retrospective nature, small sample size and lack of blinding. John Wiley and Sons Inc. 2022-03-25 2022-05 /pmc/articles/PMC9311671/ /pubmed/35333399 http://dx.doi.org/10.1111/ajd.13821 Text en © 2022 The Authors. Australasian Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Australasian College of Dermatologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Allnutt, Katherine J
Vogrin, Sara
Li, Jane
Goh, Michelle S
Brennand, Sarah
Davenport, Rachael
Chong, Alvin H
A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients
title A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients
title_full A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients
title_fullStr A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients
title_full_unstemmed A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients
title_short A long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients
title_sort long‐term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9311671/
https://www.ncbi.nlm.nih.gov/pubmed/35333399
http://dx.doi.org/10.1111/ajd.13821
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