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Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response

Immune checkpoint inhibitors have emerged as a valuable therapeutic strategy in cancer treatment. Pembrolizumab is an inhibitor of programmed cell death protein 1 (PD-1) and its ligands 1 (PD-L1) and 2 (PD-L2). Disrupting the interaction between PD-L1 expressed on the cancer cell and PD-1 transmembr...

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Detalles Bibliográficos
Autores principales: Wilkins, Matthew C, Elgamal, Mohamed, Rybkin, Igor I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684827/
https://www.ncbi.nlm.nih.gov/pubmed/34938618
http://dx.doi.org/10.7759/cureus.19739
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author Wilkins, Matthew C
Elgamal, Mohamed
Rybkin, Igor I
author_facet Wilkins, Matthew C
Elgamal, Mohamed
Rybkin, Igor I
author_sort Wilkins, Matthew C
collection PubMed
description Immune checkpoint inhibitors have emerged as a valuable therapeutic strategy in cancer treatment. Pembrolizumab is an inhibitor of programmed cell death protein 1 (PD-1) and its ligands 1 (PD-L1) and 2 (PD-L2). Disrupting the interaction between PD-L1 expressed on the cancer cell and PD-1 transmembrane protein on immune cells results in reactivation of T cell-mediated cellular immunity. This immune modulation has increased the risk of autoimmune adverse events, which can affect any organ system. Here, we present a case of delayed immune checkpoint inhibitor-induced vitiligo in a 74-year-old female with recurrent metastatic esophageal carcinoma who remains in remission more than five years after initiation of pembrolizumab.
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spelling pubmed-86848272021-12-21 Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response Wilkins, Matthew C Elgamal, Mohamed Rybkin, Igor I Cureus Dermatology Immune checkpoint inhibitors have emerged as a valuable therapeutic strategy in cancer treatment. Pembrolizumab is an inhibitor of programmed cell death protein 1 (PD-1) and its ligands 1 (PD-L1) and 2 (PD-L2). Disrupting the interaction between PD-L1 expressed on the cancer cell and PD-1 transmembrane protein on immune cells results in reactivation of T cell-mediated cellular immunity. This immune modulation has increased the risk of autoimmune adverse events, which can affect any organ system. Here, we present a case of delayed immune checkpoint inhibitor-induced vitiligo in a 74-year-old female with recurrent metastatic esophageal carcinoma who remains in remission more than five years after initiation of pembrolizumab. Cureus 2021-11-19 /pmc/articles/PMC8684827/ /pubmed/34938618 http://dx.doi.org/10.7759/cureus.19739 Text en Copyright © 2021, Wilkins et al. https://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 Dermatology
Wilkins, Matthew C
Elgamal, Mohamed
Rybkin, Igor I
Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response
title Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response
title_full Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response
title_fullStr Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response
title_full_unstemmed Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response
title_short Pembrolizumab-Induced Vitiligo in Esophageal Squamous Cell Carcinoma Patient With Durable Complete Response
title_sort pembrolizumab-induced vitiligo in esophageal squamous cell carcinoma patient with durable complete response
topic Dermatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684827/
https://www.ncbi.nlm.nih.gov/pubmed/34938618
http://dx.doi.org/10.7759/cureus.19739
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