Cost-effective use of aprepitant in multiple-day chemotherapy regimens
نویسندگان
چکیده
Background: Aprepitant is a highly effective but expensive antiemetic drug. Repeated treatment with aprepitant is required to control emesis in multiple-day chemotherapy. In the present study, cost-effectiveness analysis was carried out for the use of aprepitant in multiple-day chemotherapy, including FP (5-fluorouracil, cisplatin) for head and neck cancer and BEP (bleomycin, etoposide, cisplatin) for germ cell carcinoma. Patients and Methods: A single center, retrospective study was carried out in 46 patients receiving multiple-day chemotherapy. Standard antiemetic medication included aprepitant for 3 days for FP and for 5 days for BEP, in combination with 5-HT3 receptor antagonist and dexamethasone. In the multiple aprepitant treatment groups, aprepitant was added to the standard medication for another 2 days (FP) or 3 days (BEP). Complete protection (CP: no vomiting, no significant nausea and no rescue) was assessed during 7 days for FP or 9 days for BEP as the primary endpoint. Health states were assessed by quality-adjusted life-year (QALY) using the published utility weights. For cost-effectiveness analysis, the incremental cost-effectiveness ratio (ICER) was calculated, where the difference in the QALY was used. Results: The rate of CP was improved by multiple aprepitant treatment both in FP (54% versus 20%) and BEP (54% versus 0%). The ICERs calculated for FP and BEP were USD 17,167 or GBP 11,135/QALY gained, and USD 38,543 or GBP 25,001/QALY gained, respectively, both of which were within the threshold values configured in the UK or US. Conclusions: Repeated administration of aprepitant was found to be cost-effective for the multiple-day chemotherapy.
منابع مشابه
Fosaprepitant and aprepitant: an update of the evidence for their place in the prevention of chemotherapy-induced nausea and vomiting
INTRODUCTION The selective neurokinin-1 receptor antagonist aprepitant is effective in the treatment of acute and delayed chemotherapy-induced nausea and vomiting (CINV) associated with both moderately and highly emetogenic chemotherapy. Fosaprepitant has been developed as an intravenous prodrug of aprepitant. AIMS To update the evidence underlying the use of fosaprepitant to prevent CINV. ...
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