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Future Oncol ; 12(12): 1469-81, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26997579

ABSTRACT

AIM: APF530, extended-release granisetron, provides sustained release for ≥5 days for acute- and delayed-phase chemotherapy-induced nausea and vomiting (CINV). We compared efficacy and safety of APF530 versus ondansetron for delayed CINV after highly emetogenic chemotherapy (HEC), following a guideline-recommended three-drug regimen. METHODS: HEC patients received APF530 500 mg subcutaneously or ondansetron 0.15 mg/kg intravenously, with dexamethasone and fosaprepitant. Primary end point was delayed-phase complete response (no emesis or rescue medication). RESULTS: A higher percentage of APF530 versus ondansetron patients had delayed-phase complete response (p = 0.014). APF530 was generally well tolerated; treatment-emergent adverse event incidence was similar across arms, mostly mild-to-moderate injection-site reactions. CONCLUSION: APF530 versus the standard three-drug regimen provided superior control of delayed-phase CINV following HEC. ClinicalTrials.gov : NCT02106494.


Subject(s)
Antiemetics/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Granisetron/administration & dosage , Nausea/prevention & control , Vomiting/prevention & control , Adolescent , Adult , Aged , Aged, 80 and over , Delayed-Action Preparations/administration & dosage , Dexamethasone/administration & dosage , Dexamethasone/adverse effects , Double-Blind Method , Drug Therapy, Combination , Female , Humans , Injections, Subcutaneous , Male , Middle Aged , Morpholines/administration & dosage , Nausea/chemically induced , Ondansetron/administration & dosage , Ondansetron/adverse effects , Treatment Outcome , Vomiting/chemically induced , Young Adult
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