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Case report: Alpelisib-induced Stevens–Johnson syndrome
BACKGROUND: Alpelisib is a recently approved treatment for hormone receptor-positive, HER2-negative, PIK3CA-mutated advanced breast cancer. It has been associated with alopecia and rash, but there are no documented cases of Stevens–Johnson Syndrome (SJS) associated with this drug. Here, we detail th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554210/ https://www.ncbi.nlm.nih.gov/pubmed/36249040 http://dx.doi.org/10.3389/fonc.2022.954027 |
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author | Kurian, Christine Jane Desai, Akshay Rafferty, William Abou Hussein, Ahmed Kamel |
author_facet | Kurian, Christine Jane Desai, Akshay Rafferty, William Abou Hussein, Ahmed Kamel |
author_sort | Kurian, Christine Jane |
collection | PubMed |
description | BACKGROUND: Alpelisib is a recently approved treatment for hormone receptor-positive, HER2-negative, PIK3CA-mutated advanced breast cancer. It has been associated with alopecia and rash, but there are no documented cases of Stevens–Johnson Syndrome (SJS) associated with this drug. Here, we detail the first case of SJS associated with alpelisib. CASE DESCRIPTION: Our patient is a 60-year-old woman with a past medical history of metastatic hormone receptor-positive (ER+ 80% and PR+ 1%), HER2-negative metastatic breast cancer who presented with acute odynophagia, fevers, and diffuse body rash after receiving her first doses of alpelisib and fulvestrant in the preceding days. She presented to the emergency department after developing a whole-body rash and severe ulceration of her buccal mucosa. She was started on methylprednisolone with remarkable improvement in symptoms. CONCLUSION: This case report details the only report of SJS following alpelisib treatment. Immediate cessation of drugs and initiation of steroids are the cornerstone of treatment. Patients who experience such side effects will have to be monitored closely for long-term sequelae associated with SJS, including cutaneous, ocular, and oral sequelae, all of which can profoundly affect the quality of life for cancer patients. |
format | Online Article Text |
id | pubmed-9554210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95542102022-10-13 Case report: Alpelisib-induced Stevens–Johnson syndrome Kurian, Christine Jane Desai, Akshay Rafferty, William Abou Hussein, Ahmed Kamel Front Oncol Oncology BACKGROUND: Alpelisib is a recently approved treatment for hormone receptor-positive, HER2-negative, PIK3CA-mutated advanced breast cancer. It has been associated with alopecia and rash, but there are no documented cases of Stevens–Johnson Syndrome (SJS) associated with this drug. Here, we detail the first case of SJS associated with alpelisib. CASE DESCRIPTION: Our patient is a 60-year-old woman with a past medical history of metastatic hormone receptor-positive (ER+ 80% and PR+ 1%), HER2-negative metastatic breast cancer who presented with acute odynophagia, fevers, and diffuse body rash after receiving her first doses of alpelisib and fulvestrant in the preceding days. She presented to the emergency department after developing a whole-body rash and severe ulceration of her buccal mucosa. She was started on methylprednisolone with remarkable improvement in symptoms. CONCLUSION: This case report details the only report of SJS following alpelisib treatment. Immediate cessation of drugs and initiation of steroids are the cornerstone of treatment. Patients who experience such side effects will have to be monitored closely for long-term sequelae associated with SJS, including cutaneous, ocular, and oral sequelae, all of which can profoundly affect the quality of life for cancer patients. Frontiers Media S.A. 2022-09-28 /pmc/articles/PMC9554210/ /pubmed/36249040 http://dx.doi.org/10.3389/fonc.2022.954027 Text en Copyright © 2022 Kurian, Desai, Rafferty and Abou Hussein https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Kurian, Christine Jane Desai, Akshay Rafferty, William Abou Hussein, Ahmed Kamel Case report: Alpelisib-induced Stevens–Johnson syndrome |
title | Case report: Alpelisib-induced Stevens–Johnson syndrome |
title_full | Case report: Alpelisib-induced Stevens–Johnson syndrome |
title_fullStr | Case report: Alpelisib-induced Stevens–Johnson syndrome |
title_full_unstemmed | Case report: Alpelisib-induced Stevens–Johnson syndrome |
title_short | Case report: Alpelisib-induced Stevens–Johnson syndrome |
title_sort | case report: alpelisib-induced stevens–johnson syndrome |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554210/ https://www.ncbi.nlm.nih.gov/pubmed/36249040 http://dx.doi.org/10.3389/fonc.2022.954027 |
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