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一项比较肌肉注射格拉司琼与肌肉注射格拉司琼加地塞米松预防顺铂所致迟发性呕吐的双盲随机研究。意大利多中心研究组。

A double-blind randomized study comparing intramuscular (i.m.) granisetron with i.m. granisetron plus dexamethasone in the prevention of delayed emesis induced by cisplatin. The Italian Multicenter Study Group.

出版信息

Anticancer Drugs. 1999 Jun;10(5):465-70.

Abstract

Granisetron has been shown to exert a beneficial therapeutic effect in the prophylaxis and treatment of acute nausea and vomiting due to chemotherapy. However, limited data regarding its efficacy in the prevention and treatment of delayed emesis are available. A total of 532 patients entered this multicenter double-blind study, aimed at comparing the efficacy and safety of intramuscular (i.m.) granisetron with that of i.m. granisetron plus dexamethasone. Complete response and total control were evaluated for 3 days following the first 24 h after cisplatin administration in two groups of patients: 262 treated with granisetron 3 mg i.m. daily (plus placebo), and 265 with granisetron at the same dose plus dexamethasone 8 and 4 mg twice daily. The rate of complete response was 58.0% in the granisetron group and 78.9% in the granisetron plus dexamethasone group over days 1-3 (p<0.01). Similarly, over the same period total control was 44.7% with granisetron alone and 65.3% with granisetron plus dexamethasone (p<0.01). Local and systemic tolerability of the i.m. therapy with granisetron were satisfactory. In conclusion, granisetron plus dexamethasone showed good protection against delayed emesis due to emetogenic chemotherapy.

摘要

已证明格拉司琼在预防和治疗化疗引起的急性恶心和呕吐方面具有有益的治疗效果。然而,关于其在预防和治疗延迟性呕吐方面疗效的数据有限。共有532名患者进入了这项多中心双盲研究,旨在比较肌内注射格拉司琼与肌内注射格拉司琼加地塞米松的疗效和安全性。在两组患者中,于顺铂给药后的头24小时后的3天内评估完全缓解率和总控制率:262名患者每日肌内注射3毫克格拉司琼(加安慰剂),265名患者接受相同剂量的格拉司琼加每日两次8毫克和4毫克地塞米松。在第1 - 3天,格拉司琼组的完全缓解率为58.0%,格拉司琼加地塞米松组为78.9%(p<0.01)。同样,在同一时期,单独使用格拉司琼的总控制率为44.7%,格拉司琼加地塞米松为65.3%(p<0.01)。格拉司琼肌内治疗的局部和全身耐受性良好。总之,格拉司琼加地塞米松对致吐性化疗引起的延迟性呕吐显示出良好的保护作用。

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