Single-Dose Fosaprepitant for the Prevention of Chemotherapy-Induced Nausea and Vomiting Associated With Cisplatin Therapy: Randomized, Double-Blind Study Protocol-EASE

被引:171
作者
Grunberg, Steven [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Chua, Daniel [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Maru, Anish [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Dinis, Jose [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
DeVandry, Suzanne [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Boice, Judith A. [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Hardwick, James S. [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Beckford, Elizabeth [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Taylor, Arlene [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Carides, Alexandra [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Roila, Fausto [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Herrstedt, Jorn [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
机构
[1] Univ Vermont, Dept Med, 89 Beaumont Ave,Given Bldg E-214, Burlington, VT 05405 USA
[2] Univ Hong Kong, Hong Kong, Peoples R China
[3] SEAROC Canc Ctr, Jaipur, Rajasthan, India
[4] Portuguese Oncol Inst, Oporto, Portugal
[5] Merck Res Labs, Upper Gwynedd, PA USA
[6] Merck Res Labs, Rahway, NJ USA
[7] Santa Maria Hosp, Terni, Italy
[8] Odense Univ Hosp, DK-5000 Odense, Denmark
关键词
RECEPTOR ANTAGONIST APREPITANT; ORAL NEUROKININ-1 ANTAGONIST; PLACEBO-CONTROLLED TRIAL; CASOPITANT MESYLATE; MULTIPLE CYCLES; DELAYED NAUSEA; DEXAMETHASONE; TOLERABILITY; ANTIEMETICS; EFFICACY;
D O I
10.1200/JCO.2010.31.7859
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Addition of aprepitant, a neurokinin-1 receptor antagonist (NK1RA), to an ondansetron and dexamethasone regimen improves prevention of chemotherapy-induced nausea/vomiting (CINV), particularly during the delayed phase (DP; 25 to 120 hours). Therefore, recommended antiemetic regimens include multiple-day NK1RA administration. Preliminary data suggested that single-dose aprepitant before chemotherapy could provide CINV protection throughout the overall risk phase (OP; 0 to 120 hours). This study compared a 3-day oral aprepitant schedule to a regimen containing a single dose of the intravenous NK1RA fosaprepitant. Patients and Methods A randomized, double-blind, active-control design was used to test whether fosaprepitant is noninferior to aprepitant. Patients receiving cisplatin >= 70 mg/m(2) for the first time received ondansetron and dexamethasone with a standard aprepitant regimen (125 mg on day 1, 80 mg on day 2, 80 mg on day 3) or a single-dose fosaprepitant regimen (150 mg on day 1). The primary end point was complete response (CR; no vomiting, no rescue medication) during OP. Secondary end points were CR during DP and no vomiting during OP. Accrual of 1,113 evaluable patients per treatment arm was planned to confirm noninferiority with expected CR of 67.7% and noninferiority margin of minus 7 percentage points. Results A total of 2,322 patients were randomly assigned, and 2,247 were evaluable for efficacy. Antiemetic protection with aprepitant and fosaprepitant was equivalent within predefined bounds for noninferiority. Both regimens were well tolerated, although more frequent infusion site pain/erythema/thrombophlebitis was seen with fosaprepitant relative to aprepitant (2.7% v 0.3%, respectively). Conclusion Given with ondansetron and dexamethasone, single-dose intravenous fosaprepitant (150 mg) was noninferior to standard 3-day oral aprepitant in preventing CINV during OP and DP.
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收藏
页码:1495 / 1501
页数:7
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