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急性顺铂所致呕吐的控制——格拉司琼与大剂量甲氧氯普胺和地塞米松联合方案的比较研究。格拉司琼研究组。

The control of acute cisplatin-induced emesis--a comparative study of granisetron and a combination regimen of high-dose metoclopramide and dexamethasone. Granisetron Study Group.

作者信息

Chevallier B

机构信息

Service de Médicine Interne et Chimiothérapie, Centre Henri Becquerel, Rouen, France.

出版信息

Br J Cancer. 1993 Jul;68(1):176-80. doi: 10.1038/bjc.1993.309.

DOI:10.1038/bjc.1993.309
PMID:8391304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1968287/
Abstract

The anti-emetic efficacy and safety of granisetron, a highly selective and potent 5-HT3 receptor antagonist, was compared with that of high-dose metoclopramide plus dexamethasone in 281 patients due to receive single-day cisplatin chemotherapy (> or = 49 mg m-2). In this single-blind, multicentre study, granisetron (40 micrograms kg-1) was administered as a single prophylactic 5-min infusion. Dexamethasone (12 mg) was administered as a 30-min infusion followed by a loading dose of 3 mg kg-1 metoclopramide. A maintenance dose of metoclopramide 4 mg kg-1 was then infused over 8 h. A single prophylactic dose of granisetron was as effective as the combination regimen in the prevention of cisplatin-induced emesis. Of 143 granisetron-treated patients, 100 (70%) were complete responders (no vomiting and no or only mild nausea) compared with 93/138 (67%) patients who received the comparator regimen. Twenty-three percent of granisetron-treated patients experienced one of more adverse events compared with 33% of patients in the comparator group. No extrapyramidal reactions were reported in the granisetron group compared with 13 in comparator-treated patients (8%). This difference was significant (P < 0.05). The commonest adverse event in the granisetron group, headache (9.8%) described by the majority of patients as mild, was significantly higher than that reported in the comparator group (3% P = 0.02). Granisetron appears to be a safe and effective agent which can be used as a single agent for the prophylaxis of cisplatin-induced emesis. The simplicity of administration, a single 5-min infusion prior to chemotherapy, and the lack of somnolence or extrapyramidal reactions offer clear advantages over the comparator combination regimen.

摘要

在281例即将接受单日顺铂化疗(≥49mg/m²)的患者中,对高选择性强效5 - HT3受体拮抗剂格拉司琼的止吐疗效及安全性与大剂量甲氧氯普胺加地塞米松进行了比较。在这项单盲、多中心研究中,格拉司琼(40μg/kg)作为单次预防性5分钟输注给药。地塞米松(12mg)作为30分钟输注给药,随后给予负荷剂量3mg/kg的甲氧氯普胺。然后在8小时内输注维持剂量4mg/kg的甲氧氯普胺。单次预防性剂量的格拉司琼在预防顺铂所致呕吐方面与联合用药方案效果相当。在143例接受格拉司琼治疗的患者中,100例(70%)为完全缓解者(无呕吐且无恶心或仅有轻度恶心),而接受对照方案的138例患者中有93例(67%)为完全缓解者。接受格拉司琼治疗的患者中有23%发生了一种或多种不良事件,而对照组患者为33%。格拉司琼组未报告锥体外系反应,而对照治疗组有13例(8%)报告有锥体外系反应。这一差异具有显著性(P<0.05)。格拉司琼组最常见的不良事件是头痛(9.8%),大多数患者称其为轻度,显著高于对照组报告的发生率(3%,P = 0.02)。格拉司琼似乎是一种安全有效的药物,可作为预防顺铂所致呕吐的单一用药。其给药简单,在化疗前单次5分钟输注,且无嗜睡或锥体外系反应,与对照联合用药方案相比具有明显优势。

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