Cargando…

Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab

INTRODUCTION: Erythrodermic psoriasis (EP) is a rare variant of psoriasis. Due to its rarity, evidence supporting its treatment is limited. Patients with erythrodermic psoriasis often respond less favorably to conventional treatment and have lower biologic drug survival compared with patients with p...

Descripción completa

Detalles Bibliográficos
Autores principales: Chiang, Cheng-Ying, Tsai, Tsen-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858723/
https://www.ncbi.nlm.nih.gov/pubmed/33400156
http://dx.doi.org/10.1007/s13555-020-00480-x
_version_ 1783646653214883840
author Chiang, Cheng-Ying
Tsai, Tsen-Fang
author_facet Chiang, Cheng-Ying
Tsai, Tsen-Fang
author_sort Chiang, Cheng-Ying
collection PubMed
description INTRODUCTION: Erythrodermic psoriasis (EP) is a rare variant of psoriasis. Due to its rarity, evidence supporting its treatment is limited. Patients with erythrodermic psoriasis often respond less favorably to conventional treatment and have lower biologic drug survival compared with patients with plaque-type psoriasis. Guselkumab is an anti-interleukin-23 (IL-23) monoclonal antibody and has shown excellent and sustained treatment effect in moderate-to-severe plaque-type psoriasis. Until now, there is only one phase III open-label study reporting the effectiveness of guselkumab in this patient group. METHODS: Patients with chronic erythrodermic psoriasis who had been commenced on guselkumab were included in this retrospective study. All except one of our patients had plaque-type psoriasis prior to EP, and they met the criteria for EP before use of guselkumab. Due to inadequate response to previous treatment, including biologics, they were switched to guselkumab treatment. There was no washout period. They received guselkumab 100 mg at weeks 0 and 4, then every 8 weeks until at least week 28. Data were collected for patient demographics, Patient Area and Severity Index (PASI), and previous treatments. RESULTS: A total of 13 patients (12 male, 1 female) were included. The mean PASI improvement at weeks 4, 12, 20, and 28 was 37.5%, 60.9%, 67.5%, and 64.7%, respectively. The percentage of PASI 75 responders at weeks 4, 12, 20, and 28 was 15.4%, 38.5%, 53.9%, and 46.2%, respectively. At week 12, eight patients (61.5%) could achieve PASI 50 response. These PASI 50 responders at week 12 showed sustained and improved effectiveness during follow-up. CONCLUSION: Guselkumab is an effective biologic for treatment of moderate-to-severe plaque-type psoriasis, but the efficacy and drug survival are still compromised in EP patients. Our data describe the real-world experience of guselkumab treatment in this rare group of patients. Despite previous failure of other biologics, PASI response at week 12 is a good predictor of patient response and drug survival of guselkumab.
format Online
Article
Text
id pubmed-7858723
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer Healthcare
record_format MEDLINE/PubMed
spelling pubmed-78587232021-02-11 Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab Chiang, Cheng-Ying Tsai, Tsen-Fang Dermatol Ther (Heidelb) Case Series INTRODUCTION: Erythrodermic psoriasis (EP) is a rare variant of psoriasis. Due to its rarity, evidence supporting its treatment is limited. Patients with erythrodermic psoriasis often respond less favorably to conventional treatment and have lower biologic drug survival compared with patients with plaque-type psoriasis. Guselkumab is an anti-interleukin-23 (IL-23) monoclonal antibody and has shown excellent and sustained treatment effect in moderate-to-severe plaque-type psoriasis. Until now, there is only one phase III open-label study reporting the effectiveness of guselkumab in this patient group. METHODS: Patients with chronic erythrodermic psoriasis who had been commenced on guselkumab were included in this retrospective study. All except one of our patients had plaque-type psoriasis prior to EP, and they met the criteria for EP before use of guselkumab. Due to inadequate response to previous treatment, including biologics, they were switched to guselkumab treatment. There was no washout period. They received guselkumab 100 mg at weeks 0 and 4, then every 8 weeks until at least week 28. Data were collected for patient demographics, Patient Area and Severity Index (PASI), and previous treatments. RESULTS: A total of 13 patients (12 male, 1 female) were included. The mean PASI improvement at weeks 4, 12, 20, and 28 was 37.5%, 60.9%, 67.5%, and 64.7%, respectively. The percentage of PASI 75 responders at weeks 4, 12, 20, and 28 was 15.4%, 38.5%, 53.9%, and 46.2%, respectively. At week 12, eight patients (61.5%) could achieve PASI 50 response. These PASI 50 responders at week 12 showed sustained and improved effectiveness during follow-up. CONCLUSION: Guselkumab is an effective biologic for treatment of moderate-to-severe plaque-type psoriasis, but the efficacy and drug survival are still compromised in EP patients. Our data describe the real-world experience of guselkumab treatment in this rare group of patients. Despite previous failure of other biologics, PASI response at week 12 is a good predictor of patient response and drug survival of guselkumab. Springer Healthcare 2021-02-03 /pmc/articles/PMC7858723/ /pubmed/33400156 http://dx.doi.org/10.1007/s13555-020-00480-x Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Case Series
Chiang, Cheng-Ying
Tsai, Tsen-Fang
Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab
title Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab
title_full Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab
title_fullStr Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab
title_full_unstemmed Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab
title_short Treatment Response of Patients with Erythrodermic Psoriasis after Switching to Guselkumab
title_sort treatment response of patients with erythrodermic psoriasis after switching to guselkumab
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858723/
https://www.ncbi.nlm.nih.gov/pubmed/33400156
http://dx.doi.org/10.1007/s13555-020-00480-x
work_keys_str_mv AT chiangchengying treatmentresponseofpatientswitherythrodermicpsoriasisafterswitchingtoguselkumab
AT tsaitsenfang treatmentresponseofpatientswitherythrodermicpsoriasisafterswitchingtoguselkumab