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Palonosetron compared with ondansetron in pediatric cancer patients: multicycle analysis of a randomized Phase III study
G. Kovács, A. Wachtel, E. Basharova, T. Spinelli, P. Nicolas, E. Kabickova,
Language English Country England, Great Britain
Document type Clinical Trial, Phase III, Journal Article, Multicenter Study, Randomized Controlled Trial
NLK
PubMed Central
from 2015 to 1 year ago
ProQuest Central
from 2005-02-01 to 2020-12-31
Health & Medicine (ProQuest)
from 2005-02-01 to 2020-12-31
PubMed
28569078
DOI
10.2217/fon-2017-0189
Knihovny.cz E-resources
- MeSH
- Antiemetics administration & dosage adverse effects therapeutic use MeSH
- Quinuclidines administration & dosage adverse effects therapeutic use MeSH
- Child MeSH
- Isoquinolines administration & dosage adverse effects therapeutic use MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Neoplasms complications drug therapy MeSH
- Nausea drug therapy etiology MeSH
- Infant, Newborn MeSH
- Ondansetron administration & dosage adverse effects therapeutic use MeSH
- Child, Preschool MeSH
- Antineoplastic Agents adverse effects therapeutic use MeSH
- Treatment Outcome MeSH
- Vomiting drug therapy etiology MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase III MeSH
- Multicenter Study MeSH
- Randomized Controlled Trial MeSH
AIM: To investigate across multiple cycles the efficacy and safety of palonosetron in the prevention of chemotherapy-induced nausea and vomiting in pediatric cancer patients receiving highly or moderately emetogenic chemotherapy (HEC/MEC). PATIENTS & METHODS: Patients were randomly assigned to 10, 20 μg/kg palonosetron or 3 × 150 μg/kg ondansetron for up to four cycles of HEC/MEC. RESULTS: In all on-study chemotherapy cycles, complete response rates were higher in patients in the 20 μg/kg palonosetron group than the ondansetron group. Treatment-emergent adverse events were comparable between the palonosetron 20 μg/kg and ondansetron groups. CONCLUSION: Over four cycles of HEC/MEC, 20 μg/kg palonosetron was an efficacious and safe treatment for the prevention of chemotherapy-induced nausea and vomiting in pediatric cancer patients.
2nd Department of Pediatrics Semmelweis University Budapest Hungary
Department of Pediatrics Instituto Nacional de Enfermedades Neoplásicas Lima Peru
Helsinn Healthcare SA Lugano Switzerland
Oncohematology Center Chelyabinsk Pediatric Regional Clinical Hospital Chelyabinsk Russia
References provided by Crossref.org
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- $a AIM: To investigate across multiple cycles the efficacy and safety of palonosetron in the prevention of chemotherapy-induced nausea and vomiting in pediatric cancer patients receiving highly or moderately emetogenic chemotherapy (HEC/MEC). PATIENTS & METHODS: Patients were randomly assigned to 10, 20 μg/kg palonosetron or 3 × 150 μg/kg ondansetron for up to four cycles of HEC/MEC. RESULTS: In all on-study chemotherapy cycles, complete response rates were higher in patients in the 20 μg/kg palonosetron group than the ondansetron group. Treatment-emergent adverse events were comparable between the palonosetron 20 μg/kg and ondansetron groups. CONCLUSION: Over four cycles of HEC/MEC, 20 μg/kg palonosetron was an efficacious and safe treatment for the prevention of chemotherapy-induced nausea and vomiting in pediatric cancer patients.
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