Cargando…
Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients
BACKGROUND: Erythrodermic psoriasis (EP) remains challenging to manage because it is rare and has complex complications. Although acitretin is recommended as an appropriate choice for EP, there is a lack of large-scale evidence. OBJECTIVES: This study aims to assess the efficacy and safety of acitre...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286161/ https://www.ncbi.nlm.nih.gov/pubmed/37360416 http://dx.doi.org/10.1177/20406223231178412 |
_version_ | 1785061687322214400 |
---|---|
author | Yu, Chenyang Wu, Chao Yang, Yuyan Jin, Hongzhong |
author_facet | Yu, Chenyang Wu, Chao Yang, Yuyan Jin, Hongzhong |
author_sort | Yu, Chenyang |
collection | PubMed |
description | BACKGROUND: Erythrodermic psoriasis (EP) remains challenging to manage because it is rare and has complex complications. Although acitretin is recommended as an appropriate choice for EP, there is a lack of large-scale evidence. OBJECTIVES: This study aims to assess the efficacy and safety of acitretin as systemic monotherapy in EP patients. DESIGN: We retrospectively analyzed data from patients with EP who received at least 3 months of acitretin as systemic monotherapy during hospitalization and out-patient follow-up from January 2005 to May 2021 at the Peking Union Medical College Hospital, China. METHODS: The efficacy was clinically evaluated after 1, 2, 4, and 12 weeks of treatment, which was classified as a good response (>75% of lesions cleared), partial response (50%–75% cleared), moderate response (25–50% cleared), or no response (<25% cleared). Safety was assessed on the basis of physical examination results and significant changes in laboratory examination results after 12 weeks of treatment. RESULTS: Overall, 81 patients (79.0% men; mean age, 47.9 years) were included. The acitretin dose ranged from 20 to 60 mg/day (0.3 to 0.8 mg/kg/day). The rates of good, partial, and moderate responses were 0.0%, 2.5%, and 42.0% at 1 week; 3.7%, 34.6%, and 61.7% at 2 weeks; 29.6%, 58.0%, and 12.4% at 4 weeks; and 85.2%, 13.6%, and 1.2% at 12 weeks after treatment initiation, respectively. EP patients transformed from psoriasis vulgaris showed a higher good/partial response rate compared with that of EP patients that developed from pustular or articular psoriasis (44.6% vs. 14.3%, p = 0.035). Patients with concurrent infection showed a lower rate of good/partial response compared with that of those without concurrent infection (16.7% vs. 44.4%, p = 0.049). Adverse effects were seen in 45 (55.6%) patients in 12 weeks, and dyslipidemia (n = 31; 38.3%), xerosis (n = 24; 29.6%), and elevated liver enzymes (n = 6; 7.4%) were most commonly reported. Twenty-three patients were followed up for over 3 years, and six (26.1%) patients had EP recurrence. CONCLUSIONS: Acitretin as a systemic monotherapy showed satisfactory effectiveness for EP, especially in patients developed from psoriasis vulgaris and without infection. |
format | Online Article Text |
id | pubmed-10286161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-102861612023-06-23 Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients Yu, Chenyang Wu, Chao Yang, Yuyan Jin, Hongzhong Ther Adv Chronic Dis Original Research BACKGROUND: Erythrodermic psoriasis (EP) remains challenging to manage because it is rare and has complex complications. Although acitretin is recommended as an appropriate choice for EP, there is a lack of large-scale evidence. OBJECTIVES: This study aims to assess the efficacy and safety of acitretin as systemic monotherapy in EP patients. DESIGN: We retrospectively analyzed data from patients with EP who received at least 3 months of acitretin as systemic monotherapy during hospitalization and out-patient follow-up from January 2005 to May 2021 at the Peking Union Medical College Hospital, China. METHODS: The efficacy was clinically evaluated after 1, 2, 4, and 12 weeks of treatment, which was classified as a good response (>75% of lesions cleared), partial response (50%–75% cleared), moderate response (25–50% cleared), or no response (<25% cleared). Safety was assessed on the basis of physical examination results and significant changes in laboratory examination results after 12 weeks of treatment. RESULTS: Overall, 81 patients (79.0% men; mean age, 47.9 years) were included. The acitretin dose ranged from 20 to 60 mg/day (0.3 to 0.8 mg/kg/day). The rates of good, partial, and moderate responses were 0.0%, 2.5%, and 42.0% at 1 week; 3.7%, 34.6%, and 61.7% at 2 weeks; 29.6%, 58.0%, and 12.4% at 4 weeks; and 85.2%, 13.6%, and 1.2% at 12 weeks after treatment initiation, respectively. EP patients transformed from psoriasis vulgaris showed a higher good/partial response rate compared with that of EP patients that developed from pustular or articular psoriasis (44.6% vs. 14.3%, p = 0.035). Patients with concurrent infection showed a lower rate of good/partial response compared with that of those without concurrent infection (16.7% vs. 44.4%, p = 0.049). Adverse effects were seen in 45 (55.6%) patients in 12 weeks, and dyslipidemia (n = 31; 38.3%), xerosis (n = 24; 29.6%), and elevated liver enzymes (n = 6; 7.4%) were most commonly reported. Twenty-three patients were followed up for over 3 years, and six (26.1%) patients had EP recurrence. CONCLUSIONS: Acitretin as a systemic monotherapy showed satisfactory effectiveness for EP, especially in patients developed from psoriasis vulgaris and without infection. SAGE Publications 2023-06-20 /pmc/articles/PMC10286161/ /pubmed/37360416 http://dx.doi.org/10.1177/20406223231178412 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercialb4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Yu, Chenyang Wu, Chao Yang, Yuyan Jin, Hongzhong Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients |
title | Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients |
title_full | Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients |
title_fullStr | Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients |
title_full_unstemmed | Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients |
title_short | Systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients |
title_sort | systemic monotherapy with acitretin for erythrodermic psoriasis: results of a retrospective study of 81 patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286161/ https://www.ncbi.nlm.nih.gov/pubmed/37360416 http://dx.doi.org/10.1177/20406223231178412 |
work_keys_str_mv | AT yuchenyang systemicmonotherapywithacitretinforerythrodermicpsoriasisresultsofaretrospectivestudyof81patients AT wuchao systemicmonotherapywithacitretinforerythrodermicpsoriasisresultsofaretrospectivestudyof81patients AT yangyuyan systemicmonotherapywithacitretinforerythrodermicpsoriasisresultsofaretrospectivestudyof81patients AT jinhongzhong systemicmonotherapywithacitretinforerythrodermicpsoriasisresultsofaretrospectivestudyof81patients |