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One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients

PURPOSE: Chemotherapy-induced nausea and vomiting (CINV) is one of the most feared and disturbing adverse events of cancer treatment associated with decreased adherence to effective chemotherapy regimens. For high-risk soft tissue sarcoma patients, receiving multiple-day chemotherapy (MD-CT), antiem...

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Autores principales: Badalamenti, Giuseppe, Incorvaia, Lorena, Messina, Carlo, Musso, Emmanuela, Casarin, Alessandra, Ricciardi, Maria Rita, De Luca, Ida, Bazan, Viviana, Russo, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6660507/
https://www.ncbi.nlm.nih.gov/pubmed/30762142
http://dx.doi.org/10.1007/s00520-019-4645-3
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author Badalamenti, Giuseppe
Incorvaia, Lorena
Messina, Carlo
Musso, Emmanuela
Casarin, Alessandra
Ricciardi, Maria Rita
De Luca, Ida
Bazan, Viviana
Russo, Antonio
author_facet Badalamenti, Giuseppe
Incorvaia, Lorena
Messina, Carlo
Musso, Emmanuela
Casarin, Alessandra
Ricciardi, Maria Rita
De Luca, Ida
Bazan, Viviana
Russo, Antonio
author_sort Badalamenti, Giuseppe
collection PubMed
description PURPOSE: Chemotherapy-induced nausea and vomiting (CINV) is one of the most feared and disturbing adverse events of cancer treatment associated with decreased adherence to effective chemotherapy regimens. For high-risk soft tissue sarcoma patients, receiving multiple-day chemotherapy (MD-CT), antiemetic guidelines recommend a combination of an NK(1) receptor antagonist (NK(1)-RA), a 5-HT(3) receptor antagonist (5HT(3)-RA), and dexamethasone on each day of the antineoplastic treatment. NEPA is the first oral fixed-dose combination of a highly selective NK(1)-RA, netupitant, and second-generation 5HT(3)-RA, palonosetron. So far, no data has been published in literature about the efficacy of a single dose of NEPA in MD-CT. METHODS: We performed a prospective, non-comparative study to assess the efficacy of one shot of NEPA plus dexamethasone in sarcoma patients receiving MD-CT. The primary efficacy endpoint was a complete response (CR: no emesis, no rescue medication) during the overall phase (0–120 h) in cycle 1. The main secondary endpoints were CR during the overall phase of cycles 2 and 3. RESULTS: The primary endpoint was reached in 88.9% of patients. Cycles 2 and 3 overall CR rates were 88.9% and 82.4%, respectively. The antiemetic regimen was well tolerated. CONCLUSIONS: This pilot study showed the benefit of one shot of NEPA to prevent CINV in sarcoma patients receiving MD-chemotherapy.
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spelling pubmed-66605072019-08-07 One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients Badalamenti, Giuseppe Incorvaia, Lorena Messina, Carlo Musso, Emmanuela Casarin, Alessandra Ricciardi, Maria Rita De Luca, Ida Bazan, Viviana Russo, Antonio Support Care Cancer Original Article PURPOSE: Chemotherapy-induced nausea and vomiting (CINV) is one of the most feared and disturbing adverse events of cancer treatment associated with decreased adherence to effective chemotherapy regimens. For high-risk soft tissue sarcoma patients, receiving multiple-day chemotherapy (MD-CT), antiemetic guidelines recommend a combination of an NK(1) receptor antagonist (NK(1)-RA), a 5-HT(3) receptor antagonist (5HT(3)-RA), and dexamethasone on each day of the antineoplastic treatment. NEPA is the first oral fixed-dose combination of a highly selective NK(1)-RA, netupitant, and second-generation 5HT(3)-RA, palonosetron. So far, no data has been published in literature about the efficacy of a single dose of NEPA in MD-CT. METHODS: We performed a prospective, non-comparative study to assess the efficacy of one shot of NEPA plus dexamethasone in sarcoma patients receiving MD-CT. The primary efficacy endpoint was a complete response (CR: no emesis, no rescue medication) during the overall phase (0–120 h) in cycle 1. The main secondary endpoints were CR during the overall phase of cycles 2 and 3. RESULTS: The primary endpoint was reached in 88.9% of patients. Cycles 2 and 3 overall CR rates were 88.9% and 82.4%, respectively. The antiemetic regimen was well tolerated. CONCLUSIONS: This pilot study showed the benefit of one shot of NEPA to prevent CINV in sarcoma patients receiving MD-chemotherapy. Springer Berlin Heidelberg 2019-02-14 2019 /pmc/articles/PMC6660507/ /pubmed/30762142 http://dx.doi.org/10.1007/s00520-019-4645-3 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Badalamenti, Giuseppe
Incorvaia, Lorena
Messina, Carlo
Musso, Emmanuela
Casarin, Alessandra
Ricciardi, Maria Rita
De Luca, Ida
Bazan, Viviana
Russo, Antonio
One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients
title One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients
title_full One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients
title_fullStr One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients
title_full_unstemmed One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients
title_short One shot NEPA plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients
title_sort one shot nepa plus dexamethasone to prevent multiple-day chemotherapy in sarcoma patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6660507/
https://www.ncbi.nlm.nih.gov/pubmed/30762142
http://dx.doi.org/10.1007/s00520-019-4645-3
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