Amisulpride prevents nausea and vomiting associated with highly emetogenic chemotherapy: a randomised, double-blind, placebo-controlled, dose-ranging trial

• Published in: Supportive care in cancer 2019-07, Vol.27 (7), p.2699-2705
• Main Authors: Herrstedt, J., Summers, Y., Jordan, K., von Pawel, J., Jakobsen, A. H., Ewertz, M., Chan, S., Naik, J. D., Karthaus, M., Dubey, S., Davis, R., Fox, G. M.
• Format: Article
• Language: English
• Subjects: Anthracyclines; Aprepitant; Breast cancer; Cancer; Chemotherapy; Clinical trials; Cyclophosphamide; Double-blind studies; Drug dosages; Evidence-based medicine; Medicine; Medicine & Public Health; Nausea; Nursing; Nursing Research; Oncology; Original Article; Pain Medicine; Prevention; Rehabilitation Medicine; Vomiting
• ISSN: 0941-4355; 1433-7339
• DOI: 10.1007/s00520-018-4564-8

Purpose Chemotherapy-induced nausea and vomiting (CINV) remain significant clinical problems, especially in the delayed phase (24–120 h after chemotherapy). Amisulpride is a dopamine D 2 /D 3 -receptor antagonist previously shown to be an effective intravenous antiemetic. We conducted a randomised, double-blind study to characterise the dose response of oral amisulpride in delayed phase CINV. Methods Chemotherapy-naïve patients receiving cisplatin ≥ 70 mg/m 2 or an anthracycline-cyclophosphamide regimen for breast cancer received, on day 1, 20 mg amisulpride and 8–16 mg ondansetron intravenously followed, once daily on days 2–4, by 10, 20 or 40 mg oral amisulpride or placebo. A control group receiving standard three-drug prophylaxis was enrolled for assay sensitivity purposes. The primary endpoint was complete response (CR), defined as no emesis or rescue medication use, in the delayed phase. Results Three hundred eighteen subjects were evaluable per protocol. CR rate (24–120 h) was 20% with placebo and 46% with 10 mg amisulpride ( p  = 0.006 after multiplicity adjustment); in the three-drug control group, it was 59%. Emesis, nausea and 0–120-h CR rate were significantly improved with 10 mg amisulpride compared to placebo. Higher doses of amisulpride were not more effective than 10 mg. In patients with acute phase CR, delayed phase CR rate was 44% for placebo, 75% for 10 mg amisulpride ( p  = 0.022) and 70% for the 3-drug control. No significant differences were seen between groups in safety parameters. Conclusions Amisulpride 10 mg orally is safe and superior to placebo at preventing delayed CINV caused by highly emetogenic chemotherapy. Trial registration NCT01857232