Chiou T J, Wei C H, Hsieh R K, Fan F S, Liu J H, Chen P M
Department of Medicine, Veterans General Hospital-Taipei, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1995 Jul;56(1):23-30.
It is well known that chemotherapy-induced nausea and vomiting not only produce undesirable physical effects but also reduce patients' willingness to continue chemotherapy. The effect of a 5HT3 receptor antagonist, granisetron, on antiemesis was studied in patients who were receiving cisplatin-based chemotherapy.
Forty patients with malignant diseases, who were scheduled to receive cisplatin-based chemotherapy, were randomly assigned to receive either a single intravenous dose of granisetron (3 mg) (n = 20) or multiple doses of metoclopramide (2 mg/kg) (n = 20) as trial. The efficacy of antiemetic therapy was assessed based on the patient's subjective assessment of nausea and vomiting, and the physician's global evaluation of nausea and vomiting in the first 24 hours and during the following 6 days.
During the first 24 hours, there was a statistically significant advantage for the granisetron group in terms of prevention of both nausea and vomiting. The number of complete responders in the first 24 hours for the granisetron and metoclopramide groups was 16 (80%) and 9 (45%), respectively (p < 0.05). The control rate of anti-nausea over 6 days was 45% and 5% in the granisetron and metoclopramide groups, respectively (p < 0.001). The frequency of adverse events in the granisetron and metoclopramide groups was 10% and 45%, respectively. Analysis of laboratory data showed no significant difference between these two groups prior to and after administration of chemotherapy.
A single 5-minute infusion of 3 mg granisetron was more effective and produced a less adverse effect than multiple doses of metoclopramide in controlling chemotherapy-induced emesis, both in the first 24 hours and over a 6-day period.
众所周知,化疗引起的恶心和呕吐不仅会产生不良的身体影响,还会降低患者继续化疗的意愿。本研究在接受顺铂化疗的患者中探讨了5HT3受体拮抗剂格拉司琼的止吐效果。
40例计划接受顺铂化疗的恶性疾病患者被随机分为两组,一组接受单次静脉注射格拉司琼(3毫克)(n = 20),另一组接受多次注射甲氧氯普胺(2毫克/千克)(n = 20)作为试验。根据患者对恶心和呕吐的主观评估以及医生在前24小时和接下来6天对恶心和呕吐的整体评估来评估止吐治疗的效果。
在最初的24小时内,格拉司琼组在预防恶心和呕吐方面具有统计学上的显著优势。格拉司琼组和甲氧氯普胺组在最初24小时内的完全缓解者数量分别为16例(80%)和9例(45%)(p < 0.05)。格拉司琼组和甲氧氯普胺组在6天内的抗恶心控制率分别为45%和5%(p < 0.001)。格拉司琼组和甲氧氯普胺组的不良事件发生率分别为10%和45%。化疗前后两组实验室数据的分析显示无显著差异。
在控制化疗引起的呕吐方面,单次5分钟输注3毫克格拉司琼在最初24小时和6天期间均比多次注射甲氧氯普胺更有效且不良反应更少。