Netupitant/palonosetron (NEPA; Akynzeo®) combination in prevention of the nausea and vomiting in patients with breast cancer receiving anthracyclinbased chemotherapy
- Authors: Kedrova A.G.1,2, Berishvili A.I.2
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Affiliations:
- Federal Research and Clinical Center for Specialized Medical Care and Medical Technologies, Federal Biomedical Agency of the Russian Federation
- Federal Research and Clinical Center, Federal Biomedical Agency
- Issue: Vol 19, No 3 (2023)
- Pages: 54-62
- Section: MAMMOLOGY. REVIEWS
- Published: 27.10.2023
- URL: https://ojrs.abvpress.ru/ojrs/article/view/1138
- DOI: https://doi.org/10.17650/1994-4098-2023-19-3-54-62
- ID: 1138
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Abstract
Chemotherapy-induced nausea and vomiting is a common problem during cancer treatment, especially in breast cancer patients with anthracycline/cyclophosphamide (ас) chemotherapy. Netupitant/palonosetron (NEPA; Akynzeo®) is a fixed-dose combination of two drugs (netupitant, a neurokinin 1 receptor antagonist; and palonosetron, a serotonin 3 receptor antagonist) which target two diferent signalling pathways involved in the induction of vomiting. Approved for use in the prevention of acute and delayed chemotherapy-induced nausea and vomiting in adults, netupitant/palonosetron is given orally or via intravenous infusion as a single dose prior to chemotherapy. In clinical trials, high proportions of patients who received netupitant/palonosetron (used in combination with the corticosteroid dexamethasone) prior to chemotherapy reported no vomiting, no requirement for rescue medication, and no signifcant nausea in the 5 days post chemotherapy. Both the oral and intravenous formulations of the drug combination are well tolerated. Thus, netupitant/palonosetron is a simple, convenient and efective drug combination for the prevention of acute and delayed xhemotherapy-induced nausea and vomiting in patients receiving chemotherapy that has a moderate to high emetogenic potential.
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About the authors
A. G. Kedrova
Federal Research and Clinical Center for Specialized Medical Care and Medical Technologies, Federal Biomedical Agency of the Russian Federation; Federal Research and Clinical Center, Federal Biomedical Agency
Author for correspondence.
Email: kedrova.anna@gmail.com
ORCID iD: 0000-0003-1031-9376
Anna Genrikhovna Kedrova - Department of Oncology CCSMCMT, FBARF; Department of Obstetrics and Gynecology, Academy of Postgraduate Education Federal Research and Clinical Center, FBA.
28 Orekhovyy Bulvar, Moscow 115682; 91 Volokolamskoe Shosse, Moscow 125371
Russian FederationA. I. Berishvili
Federal Research and Clinical Center, Federal Biomedical Agency
Email: aberishvili@yandex.ru
Alexander Ilyich Berishvili Department of Obstetrics and Gynecology, Academy of Postgraduate Education.
91 Volokolamskoe Shosse, Moscow 125371
Russian FederationReferences
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