首页> 外文期刊>Journal of Clinical Oncology >Comparison of single-dose oral granisetron versus intravenous ondansetron in the prevention of nausea and vomiting induced by moderately emetogenic chemotherapy: a multicenter, double-blind, randomized parallel study.
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Comparison of single-dose oral granisetron versus intravenous ondansetron in the prevention of nausea and vomiting induced by moderately emetogenic chemotherapy: a multicenter, double-blind, randomized parallel study.

机译:单剂量口服格拉司琼与静脉使用恩丹西酮在预防中度致癌化学疗法引起的恶心和呕吐方面的比较:一项多中心,双盲,随机平行研究。

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PURPOSE: The antiemetic effectiveness and safety of single-dose oral granisetron were compared with intravenous (I.V.) ondansetron in chemotherapy-naive patients who received moderately emetogenic chemotherapy. PATIENTS AND METHODS: In this double-blind, parallel-group study, patients naive to emetogenic chemotherapy (N = 1,085) who were scheduled to receive cyclophosphamide- (500 to 1,200 mg/m2) or carboplatin (> or = 300 mg/m2) based chemotherapy, were randomized to receive either oral granisetron (n = 542) or I.V. ondansetron (n = 543). Efficacy assessments included the proportion of patients in each treatment group with total control over the 24 and 48 hours following chemotherapy initiation, as well as incidence and severity of nausea and emesis and use of antiemetic rescue medication. Prophylactic corticosteroids were allowed. Safety assessment was based on patients' reports of adverse experiences. RESULTS: Approximately 80% of patients received prophylactic corticosteroids. Single-dose oral granisetron (2 mg) and I.V. ondansetron (32 mg) resulted in equivalent levels of total emetic control during the first 48 hours after chemotherapy. The proportion of nausea- and emesis-free patients at 24 and 48 hours were also approximately equivalent. The most commonly reported adverse experiences were headache, asthenia, and constipation. More patients who received ondonsetron than granisetron reported dizziness (9.6% v 5.4%, respectively; P = .011) and abnormal vision (4.2% v 0.6%, respectively; P < .001). CONCLUSION: A single oral dose of granisetron (2 mg) resulted in equivalent levels of antiemetic protection as I.V. ondansetron (32 mg). Both agents were well tolerated, although more dizziness and abnormal vision were reported with ondansetron. Because the two antiemetic regimens exhibited equivalent efficacies, additional factors such as convenience and cost of therapy should be considered.
机译:目的:比较初次接受化学治疗的初生化疗患者中单剂量口服格拉司琼与静脉内(I.V.)恩丹西酮的止吐效果和安全性。患者与方法:在这项双盲,平行组研究中,未接受过生胎化疗(N = 1,085)的患者计划接受环磷酰胺(500至1,200 mg / m2)或卡铂(>或= 300 mg / m2) )为基础的化疗,随机接受口服Granisetron(n = 542)或静脉注射恩丹西酮(n = 543)。疗效评估包括在开始化疗后24和48小时内完全控制的每个治疗组中患者的比例,以及恶心和呕吐的发生率和严重程度以及使用止吐急救药物。预防性使用糖皮质激素。安全性评估基于患者不良经历的报告。结果:大约80%的患者接受了预防性糖皮质激素治疗。单剂量口服Granisetron(2 mg)和I.V.恩丹西酮(32毫克)在化疗后的最初48小时内产生了相同水平的呕吐控制。 24小时和48小时无恶心和呕吐的患者比例也大致相当。最常见的不良反应是头痛,乏力和便秘。接受恩多西酮治疗的患者多于Granisetron患者,头晕(分别为9.6%v 5.4%; P = .011)和视力异常(分别为4.2%v 0.6%; P <.001)。结论:单次口服格拉司琼(2 mg)可产生与I.V.相同水平的止吐保护。恩丹西酮(32毫克)。两种药物均具有良好的耐受性,尽管据报道恩丹西酮有更多的头晕和视力异常。由于两种止吐方案均具有相同的疗效,因此应考虑其他因素,例如便利性和治疗费用。

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