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Hypersensitivity to Carboplatin in Children with Malignancy
Purpose: Carboplatin-based regimens have proven efficacy in children with cancer. However, the development of hypersensitivity reactions (HSRs) may have a negative impact on treatment intensity and patients’ outcome. The aim of this review is to summarize the incidence and the clinical features of H...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388748/ https://www.ncbi.nlm.nih.gov/pubmed/28446876 http://dx.doi.org/10.3389/fphar.2017.00201 |
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author | Ruggiero, Antonio Rizzo, Daniela Catalano, Martina Attinà, Giorgio Riccardi, Riccardo |
author_facet | Ruggiero, Antonio Rizzo, Daniela Catalano, Martina Attinà, Giorgio Riccardi, Riccardo |
author_sort | Ruggiero, Antonio |
collection | PubMed |
description | Purpose: Carboplatin-based regimens have proven efficacy in children with cancer. However, the development of hypersensitivity reactions (HSRs) may have a negative impact on treatment intensity and patients’ outcome. The aim of this review is to summarize the incidence and the clinical features of HSRs occurring in children with cancer treated with carboplatin and their impact on treatment efficacy. Methods: Data were collected by searching for relevant studies on the incidence, clinical features and management of possible side effects about the use of carboplatin in children, published from March 1987 to October 2016 in the PubMed database. Results: Carboplatin HSRs present with mild/moderate to severe clinical patterns. The risk of HSR is related to the cumulative number of infusions. Moreover, a greater risk of developing an HSR has been observed in younger patients than in older age groups of children; risk is also greater in girls and in patients with a prior history of allergy to other drugs. Management options include cessation of carboplatin and switching to another agent, premedication with antihistamines and/or corticosteroids, and carboplatin desensitization. For sensitized patients who have obtained benefits from carboplatin, the continuation of the treatment is desirable and desensitization protocols have showed promising results. Conclusion: Clinicians must not underestimate the potential risk and occurrence of carboplatin HSRs in the pediatric population in order to outline adequate management strategies. Desensitization protocols should be considered for patients sensitive to carboplatin in order to avoid having to discontinue an effective chemotherapy. |
format | Online Article Text |
id | pubmed-5388748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53887482017-04-26 Hypersensitivity to Carboplatin in Children with Malignancy Ruggiero, Antonio Rizzo, Daniela Catalano, Martina Attinà, Giorgio Riccardi, Riccardo Front Pharmacol Pharmacology Purpose: Carboplatin-based regimens have proven efficacy in children with cancer. However, the development of hypersensitivity reactions (HSRs) may have a negative impact on treatment intensity and patients’ outcome. The aim of this review is to summarize the incidence and the clinical features of HSRs occurring in children with cancer treated with carboplatin and their impact on treatment efficacy. Methods: Data were collected by searching for relevant studies on the incidence, clinical features and management of possible side effects about the use of carboplatin in children, published from March 1987 to October 2016 in the PubMed database. Results: Carboplatin HSRs present with mild/moderate to severe clinical patterns. The risk of HSR is related to the cumulative number of infusions. Moreover, a greater risk of developing an HSR has been observed in younger patients than in older age groups of children; risk is also greater in girls and in patients with a prior history of allergy to other drugs. Management options include cessation of carboplatin and switching to another agent, premedication with antihistamines and/or corticosteroids, and carboplatin desensitization. For sensitized patients who have obtained benefits from carboplatin, the continuation of the treatment is desirable and desensitization protocols have showed promising results. Conclusion: Clinicians must not underestimate the potential risk and occurrence of carboplatin HSRs in the pediatric population in order to outline adequate management strategies. Desensitization protocols should be considered for patients sensitive to carboplatin in order to avoid having to discontinue an effective chemotherapy. Frontiers Media S.A. 2017-04-12 /pmc/articles/PMC5388748/ /pubmed/28446876 http://dx.doi.org/10.3389/fphar.2017.00201 Text en Copyright © 2017 Ruggiero, Rizzo, Catalano, Attinà and Riccardi. http://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) or licensor 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 | Pharmacology Ruggiero, Antonio Rizzo, Daniela Catalano, Martina Attinà, Giorgio Riccardi, Riccardo Hypersensitivity to Carboplatin in Children with Malignancy |
title | Hypersensitivity to Carboplatin in Children with Malignancy |
title_full | Hypersensitivity to Carboplatin in Children with Malignancy |
title_fullStr | Hypersensitivity to Carboplatin in Children with Malignancy |
title_full_unstemmed | Hypersensitivity to Carboplatin in Children with Malignancy |
title_short | Hypersensitivity to Carboplatin in Children with Malignancy |
title_sort | hypersensitivity to carboplatin in children with malignancy |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388748/ https://www.ncbi.nlm.nih.gov/pubmed/28446876 http://dx.doi.org/10.3389/fphar.2017.00201 |
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