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Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma

Melanoma is widely treated with programmed cell death‐1 (PD‐1) inhibitors. As part of their anti‐tumor immunity effect, they increase the susceptibility to cutaneous immune‐related adverse events (cIRAE) among other autoimmune effects. To characterize the manifestations of cIRAE in melanoma patients...

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Autores principales: Shreberk‐Hassidim, Rony, Aizenbud, Lilach, Lussheimer, Shalev, Thomaidou, Elena, Bdolah‐Abram, Tali, Merims, Sharon, Popovtzer, Aron, Maly, Alex, Lotem, Michal, Zlotogorski, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786241/
https://www.ncbi.nlm.nih.gov/pubmed/36190005
http://dx.doi.org/10.1111/dth.15747
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author Shreberk‐Hassidim, Rony
Aizenbud, Lilach
Lussheimer, Shalev
Thomaidou, Elena
Bdolah‐Abram, Tali
Merims, Sharon
Popovtzer, Aron
Maly, Alex
Lotem, Michal
Zlotogorski, Abraham
author_facet Shreberk‐Hassidim, Rony
Aizenbud, Lilach
Lussheimer, Shalev
Thomaidou, Elena
Bdolah‐Abram, Tali
Merims, Sharon
Popovtzer, Aron
Maly, Alex
Lotem, Michal
Zlotogorski, Abraham
author_sort Shreberk‐Hassidim, Rony
collection PubMed
description Melanoma is widely treated with programmed cell death‐1 (PD‐1) inhibitors. As part of their anti‐tumor immunity effect, they increase the susceptibility to cutaneous immune‐related adverse events (cIRAE) among other autoimmune effects. To characterize the manifestations of cIRAE in melanoma patients treated with PD‐1 inhibitors, and evaluate the correlation with tumor response. A retrospective study of 95 metastatic malignant melanoma patients treated with PD‐1 inhibitors at the Hadassah Medical Center during 2013–2016. The most common cIRAE was pruritus reported by 39 (41%) patients. All other cIRAE were noted in 34 patients (35.8%), of which the most common cutaneous manifestation was vitiligo, demonstrated in 17 patients (17.9%) followed by various rashes (7.4%, including erythema multiforme, oral lichen planus, photosensitive rash, insect bite‐like reaction, and urticaria), psoriasiform rash (3.2%), bullous pemphigoid (3.2%), and eczema (1%). Interestingly, higher response rates to immunotherapy were demonstrated in patients who developed pruritus (85%) and cIRAE (88%), with lower mortality rates in the cIRAE group (38.2%) versus the non‐cIRAE group (70.5%, p = 0.002). cIRAE are common among malignant melanoma patients treated with PD‐1 inhibitors and may be a marker for favorable prognosis.
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spelling pubmed-97862412022-12-27 Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma Shreberk‐Hassidim, Rony Aizenbud, Lilach Lussheimer, Shalev Thomaidou, Elena Bdolah‐Abram, Tali Merims, Sharon Popovtzer, Aron Maly, Alex Lotem, Michal Zlotogorski, Abraham Dermatol Ther Original Articles Melanoma is widely treated with programmed cell death‐1 (PD‐1) inhibitors. As part of their anti‐tumor immunity effect, they increase the susceptibility to cutaneous immune‐related adverse events (cIRAE) among other autoimmune effects. To characterize the manifestations of cIRAE in melanoma patients treated with PD‐1 inhibitors, and evaluate the correlation with tumor response. A retrospective study of 95 metastatic malignant melanoma patients treated with PD‐1 inhibitors at the Hadassah Medical Center during 2013–2016. The most common cIRAE was pruritus reported by 39 (41%) patients. All other cIRAE were noted in 34 patients (35.8%), of which the most common cutaneous manifestation was vitiligo, demonstrated in 17 patients (17.9%) followed by various rashes (7.4%, including erythema multiforme, oral lichen planus, photosensitive rash, insect bite‐like reaction, and urticaria), psoriasiform rash (3.2%), bullous pemphigoid (3.2%), and eczema (1%). Interestingly, higher response rates to immunotherapy were demonstrated in patients who developed pruritus (85%) and cIRAE (88%), with lower mortality rates in the cIRAE group (38.2%) versus the non‐cIRAE group (70.5%, p = 0.002). cIRAE are common among malignant melanoma patients treated with PD‐1 inhibitors and may be a marker for favorable prognosis. John Wiley & Sons, Inc. 2022-08-09 2022-10 /pmc/articles/PMC9786241/ /pubmed/36190005 http://dx.doi.org/10.1111/dth.15747 Text en © 2022 The Authors. Dermatologic Therapy published by Wiley Periodicals LLC. 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 Articles
Shreberk‐Hassidim, Rony
Aizenbud, Lilach
Lussheimer, Shalev
Thomaidou, Elena
Bdolah‐Abram, Tali
Merims, Sharon
Popovtzer, Aron
Maly, Alex
Lotem, Michal
Zlotogorski, Abraham
Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma
title Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma
title_full Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma
title_fullStr Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma
title_full_unstemmed Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma
title_short Dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma
title_sort dermatological adverse events under programmed cell death‐1 inhibitors as a prognostic marker in metastatic melanoma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786241/
https://www.ncbi.nlm.nih.gov/pubmed/36190005
http://dx.doi.org/10.1111/dth.15747
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