Ritter H L, Gralla R J, Hall S W, Wada J K, Friedman C, Hand L, Fitts D
Toledo Clinic, Inc., Hematology-Oncology Department, Ohio 43623, USA.
Cancer Invest. 1998;16(2):87-93. doi: 10.3109/07357909809039762.
The safety and efficacy of granisetron (10 micrograms/kg and 40 micrograms/kg) were evaluated during a second (n = 393) and third (n = 200) cycle of chemotherapy in this multicenter, double-blind, randomized, parallel-group study. Granisetron was administered as a single intravenous dose before the start of cisplatin chemotherapy (> or = 60 mg/m2). Total control (no vomiting, no retching, no nausea, and no use of antiemetic rescue medication) after the first 24 hr following chemotherapy was achieved in 40% and 49% of patients in Cycles 2 and 3, respectively, for the 10 micrograms/kg group, and in 42% and 38% of patients in Cycles 2 and 3, respectively, for the 40 micrograms/kg group. Both dose levels of granisetron were well tolerated. The results demonstrate comparable efficacy between the 10 micrograms/kg and 40 micrograms/kg doses of granisetron in preventing nausea and vomiting during repeat cycles of high-dose cisplatin-based chemotherapy. The results of this study show that granisetron 10 micrograms/kg is safe and well tolerated, and remains effective with repeat cycle use.
在这项多中心、双盲、随机、平行组研究中,对格拉司琼(10微克/千克和40微克/千克)在化疗的第二个周期(n = 393)和第三个周期(n = 200)期间的安全性和有效性进行了评估。在顺铂化疗(≥60毫克/平方米)开始前,将格拉司琼作为单次静脉注射剂量给药。对于10微克/千克组,化疗后最初24小时内的完全控制(无呕吐、无干呕、无恶心且未使用止吐急救药物)在第2周期和第3周期分别达到40%和49%的患者;对于40微克/千克组,在第2周期和第3周期分别达到42%和38%的患者。格拉司琼的两个剂量水平耐受性均良好。结果表明,在基于高剂量顺铂的重复化疗周期中,10微克/千克和40微克/千克剂量的格拉司琼在预防恶心和呕吐方面疗效相当。本研究结果表明,10微克/千克的格拉司琼安全且耐受性良好,重复周期使用时仍有效。