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Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions
Alpelisib is a specific oral PI3K inhibitor used combined with fulvestrant for the treatment of patients with HR+/HER2–/PIK3CA-mutated metastatic breast cancer. Adverse drug reactions with alpelisib are common, including hyperglycemia and rash. Here we describe extraordinary and life-threatening rea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322120/ https://www.ncbi.nlm.nih.gov/pubmed/37086483 http://dx.doi.org/10.1093/oncolo/oyad092 |
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author | Schutte, Tim Zeverijn, Laurien J Geurts, Birgit S de Wit, Gijsbrecht F Kok, Marleen Opdam, Frans L |
author_facet | Schutte, Tim Zeverijn, Laurien J Geurts, Birgit S de Wit, Gijsbrecht F Kok, Marleen Opdam, Frans L |
author_sort | Schutte, Tim |
collection | PubMed |
description | Alpelisib is a specific oral PI3K inhibitor used combined with fulvestrant for the treatment of patients with HR+/HER2–/PIK3CA-mutated metastatic breast cancer. Adverse drug reactions with alpelisib are common, including hyperglycemia and rash. Here we describe extraordinary and life-threatening reactions beyond skin rash in two patients with progressive PIK3CA-mutated metastatic cancer in whom alpelisib was initiated. Case-A (vaginal cancer): After 10 days on treatment, she developed dry eyes, generalized rash and itching. Alpelisib was interrupted and symptomatic treatment initiated. Because of an initial tumor response, a rechallenge was done. Ninety minutes after a reduced dose of alpelisib, she developed an anaphylactic reaction with angioedema, hypotension, and skin rash. Case-B (breast cancer): After 11 days on treatment, she developed skin rash and alpelisib was interrupted. At re-initiation, she felt tingles in her face and ears and some skin erythema. Given the mild rash, a second rechallenge with premedication was performed. Ninety minutes after a reduced dose of alpelisib, she developed a type-1 allergic reaction with angioedema, tingles, and skin rash. In both cases, a type-1 allergic reaction was diagnosed and symptomatic treatment was initiated, alpelisib was permanently discontinued and the patients fully recovered the next week(s). This report underlines the critical importance to consider type-I allergic reactions in the differential diagnosis in cases of rash associated with alpelisib. Even if a reaction develops after days on treatment, a type-I allergic reaction cannot be excluded. A rechallenge can be dangerous and should always be well contemplated or even avoided. |
format | Online Article Text |
id | pubmed-10322120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103221202023-07-06 Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions Schutte, Tim Zeverijn, Laurien J Geurts, Birgit S de Wit, Gijsbrecht F Kok, Marleen Opdam, Frans L Oncologist Breast Cancer Alpelisib is a specific oral PI3K inhibitor used combined with fulvestrant for the treatment of patients with HR+/HER2–/PIK3CA-mutated metastatic breast cancer. Adverse drug reactions with alpelisib are common, including hyperglycemia and rash. Here we describe extraordinary and life-threatening reactions beyond skin rash in two patients with progressive PIK3CA-mutated metastatic cancer in whom alpelisib was initiated. Case-A (vaginal cancer): After 10 days on treatment, she developed dry eyes, generalized rash and itching. Alpelisib was interrupted and symptomatic treatment initiated. Because of an initial tumor response, a rechallenge was done. Ninety minutes after a reduced dose of alpelisib, she developed an anaphylactic reaction with angioedema, hypotension, and skin rash. Case-B (breast cancer): After 11 days on treatment, she developed skin rash and alpelisib was interrupted. At re-initiation, she felt tingles in her face and ears and some skin erythema. Given the mild rash, a second rechallenge with premedication was performed. Ninety minutes after a reduced dose of alpelisib, she developed a type-1 allergic reaction with angioedema, tingles, and skin rash. In both cases, a type-1 allergic reaction was diagnosed and symptomatic treatment was initiated, alpelisib was permanently discontinued and the patients fully recovered the next week(s). This report underlines the critical importance to consider type-I allergic reactions in the differential diagnosis in cases of rash associated with alpelisib. Even if a reaction develops after days on treatment, a type-I allergic reaction cannot be excluded. A rechallenge can be dangerous and should always be well contemplated or even avoided. Oxford University Press 2023-04-22 /pmc/articles/PMC10322120/ /pubmed/37086483 http://dx.doi.org/10.1093/oncolo/oyad092 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Breast Cancer Schutte, Tim Zeverijn, Laurien J Geurts, Birgit S de Wit, Gijsbrecht F Kok, Marleen Opdam, Frans L Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions |
title | Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions |
title_full | Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions |
title_fullStr | Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions |
title_full_unstemmed | Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions |
title_short | Beyond Skin Rash: Alpelisib-Induced Anaphylactic Reactions |
title_sort | beyond skin rash: alpelisib-induced anaphylactic reactions |
topic | Breast Cancer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322120/ https://www.ncbi.nlm.nih.gov/pubmed/37086483 http://dx.doi.org/10.1093/oncolo/oyad092 |
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