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    FDA approves rolapitant to prevent chemotherapy-induced nausea and vomiting

    Daniel RaccuiaDaniel RaccuiaLisa HolleLisa HolleOn September 2, 2015, FDA approved rolapitant (Varubi; Tesaro) in combination with other antiemetic agents to prevent delayed nausea and vomiting associated with initial and repeat courses of emetogenic cancer chemotherapy, including, but not limited to, highly emetogenic chemotherapy. 

    Chemotherapy-induced nausea and vomiting can be a severely debilitating side effect of cancer therapy that can impair quality of life, functional ability, and treatment adherence. Without appropriate prophylaxis, moderately emetogenic chemotherapy can induce nausea and vomiting in 30% to 90% of patients; highly emetogenic chemotherapy can induce nausea and vomiting in more than 90% of patients. Nausea and vomiting can last up to five days after initiation of chemotherapy and is divided into two phases, acute (0-24 hours) and delayed (24-120 hours).

    The activation of the substance P/neurokinin 1 (NK1) receptor signaling pathway is thought to be the primary mediator of nausea and vomiting in the delayed phase. Rolapitant is a novel NK1 receptor antagonist that maintains >90% receptor binding up to five days after a single 180 mg dose. In addition, rolapitant does not inhibit or induce cytochrome P450 (CYP)-3A4 and may provide an alternative with fewer potential drug interactions that the other approved NK1 receptor antagonists.

    See also: FDA approves PAH treatment

    Efficacy

    The rolapitant approval was based on data from three double-blind, randomized, active-controlled trials. Studies 1 and 2 evaluated 1,070 patients receiving their first cycle of highly emetogenic cisplatin-based chemotherapy, while study 3 evaluated 1,332 patients receiving their first cycle of moderately emetogenic chemotherapy (or an anthracycline plus cyclophosphamide).

    In each of these studies, patients were given rolapitant 180 mg or placebo orally one to two hours before initiation of chemotherapy, and all patients received active control. In studies 1 and 2, active control consisted of intravenous granisetron (10 mcg/kg) plus oral dexamethasone (20 mg) 30 minutes before chemotherapy initiation, and twice-daily oral dexamethasone (8 mg) on days 2 through 4. In study 3, active control consisted of oral granisetron (2 mg) plus oral dexamethasone (20 mg) 30 minutes before chemotherapy initiation, and oral granisetron (2 mg) on days 2 and 3.

    Efficacy was measured as percentage of patients with a complete response in the delayed phase, defined as no emesis or use of rescue medications for 24 to 120 hours after the initiation of chemotherapy. Researchers assessed endpoint results using daily diaries patients maintained over the 120-hour study period.

    In the pooled analysis of studies 1 and 2, 71% of patients in the rolapitant group achieved a complete response, compared with 60% in the active control group (OR 1.6, 95% CI 1.3-2.1; P=0.0001). In the third study, 71% in the rolapitant group achieved complete response, compared with 62% in the active control group (OR 1.6, 95% CI 1.2-2.0; P=0.0002).

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    Daniel S. Raccuia, PharmD candidate 2016
    Daniel S. Raccuia is a 2016 PharmD candidate at University of Connecticut School of Pharmacy, Storrs, Conn.
    Lisa M. Holle, PharmD, BCOP, FHOPA
    Lisa M. Holle, PharmD, BCOP, FHOPA is an assistant clinical professor, University of Connecticut School of Pharmacy, Storrs, Conn.

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