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Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease

Chronic graft-versus host disease (cGVHD) occurs in 30% to 70% of patients undergoing allogeneic hematopoietic cell transplantation (HCT). Cutaneous cGVHD affects 75% of cGVHD patients, causing discomfort, limiting the range of movement, and increasing the risk of wound infections. Furthermore, syst...

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Autores principales: Kim, Yoo Jung, Lee, Gun Ho, Kwong, Bernice Y, Martires, Kathryn J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977575/
https://www.ncbi.nlm.nih.gov/pubmed/32025391
http://dx.doi.org/10.7759/cureus.6462
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author Kim, Yoo Jung
Lee, Gun Ho
Kwong, Bernice Y
Martires, Kathryn J
author_facet Kim, Yoo Jung
Lee, Gun Ho
Kwong, Bernice Y
Martires, Kathryn J
author_sort Kim, Yoo Jung
collection PubMed
description Chronic graft-versus host disease (cGVHD) occurs in 30% to 70% of patients undergoing allogeneic hematopoietic cell transplantation (HCT). Cutaneous cGVHD affects 75% of cGVHD patients, causing discomfort, limiting the range of movement, and increasing the risk of wound infections. Furthermore, systemic immunosuppression is often needed to treat cGVHD and long-term use can lead to adverse events. Optimal use of skin-directed therapies is integral to the management of cutaneous cGVHD and may decrease the amount of systemic immunosuppression required. This study reviewed English-language articles published from 1990 to 2017 that evaluated the effect of skin-directed treatments for cutaneous cGVHD. A total of 201 papers were identified, 164 articles were screened, 46 were read, and 18 publications were utilized in the review. Skin-directed treatments for cGVHD included topical steroids, topical calcineurin inhibitors, psoralen with ultraviolet A (PUVA) irradiation, ultraviolet A1 (UVA1) irradiation, and ultraviolet B (UVB) irradiation. We report the number of complete remissions, partial remissions, and systemic immunosuppression reduction in each study, as available. Twenty-two out of 30 (73.3%) patients experienced overall improvement with topical calcineurin inhibitors. At least 26 out of 76 patients (34.2%) receiving PUVA experienced complete remission, and 30 out of 76 patients (39.5%) experienced partial remission. In UVA1 studies, 44 out of 52 (84.6%) patients experienced overall improvement. In UVB studies, nine out of 14 patients (64.3%) experienced complete remission and four out of 14 patients (28.6%) experienced partial remission. As more HCTs are performed, more individuals will develop cGVHD. Awareness and optimal use of skin-directed therapies for cutaneous cGVHD may help improve patient outcomes and quality of life.
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spelling pubmed-69775752020-02-05 Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease Kim, Yoo Jung Lee, Gun Ho Kwong, Bernice Y Martires, Kathryn J Cureus Transplantation Chronic graft-versus host disease (cGVHD) occurs in 30% to 70% of patients undergoing allogeneic hematopoietic cell transplantation (HCT). Cutaneous cGVHD affects 75% of cGVHD patients, causing discomfort, limiting the range of movement, and increasing the risk of wound infections. Furthermore, systemic immunosuppression is often needed to treat cGVHD and long-term use can lead to adverse events. Optimal use of skin-directed therapies is integral to the management of cutaneous cGVHD and may decrease the amount of systemic immunosuppression required. This study reviewed English-language articles published from 1990 to 2017 that evaluated the effect of skin-directed treatments for cutaneous cGVHD. A total of 201 papers were identified, 164 articles were screened, 46 were read, and 18 publications were utilized in the review. Skin-directed treatments for cGVHD included topical steroids, topical calcineurin inhibitors, psoralen with ultraviolet A (PUVA) irradiation, ultraviolet A1 (UVA1) irradiation, and ultraviolet B (UVB) irradiation. We report the number of complete remissions, partial remissions, and systemic immunosuppression reduction in each study, as available. Twenty-two out of 30 (73.3%) patients experienced overall improvement with topical calcineurin inhibitors. At least 26 out of 76 patients (34.2%) receiving PUVA experienced complete remission, and 30 out of 76 patients (39.5%) experienced partial remission. In UVA1 studies, 44 out of 52 (84.6%) patients experienced overall improvement. In UVB studies, nine out of 14 patients (64.3%) experienced complete remission and four out of 14 patients (28.6%) experienced partial remission. As more HCTs are performed, more individuals will develop cGVHD. Awareness and optimal use of skin-directed therapies for cutaneous cGVHD may help improve patient outcomes and quality of life. Cureus 2019-12-25 /pmc/articles/PMC6977575/ /pubmed/32025391 http://dx.doi.org/10.7759/cureus.6462 Text en Copyright © 2019, Kim et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Transplantation
Kim, Yoo Jung
Lee, Gun Ho
Kwong, Bernice Y
Martires, Kathryn J
Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease
title Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease
title_full Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease
title_fullStr Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease
title_full_unstemmed Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease
title_short Evidence-based, Skin-directed Treatments for Cutaneous Chronic Graft-versus-host Disease
title_sort evidence-based, skin-directed treatments for cutaneous chronic graft-versus-host disease
topic Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977575/
https://www.ncbi.nlm.nih.gov/pubmed/32025391
http://dx.doi.org/10.7759/cureus.6462
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