Chevallier B, Marty M, Paillarse J M
Centre Anti-Cancéreux Henri Becquerel, Rouen, France.
Br J Cancer. 1994 Dec;70(6):1171-5. doi: 10.1038/bjc.1994.467.
This double-blind multicentre study has been carried out in order to confirm the improvement of ondansetron's antiemetic efficacy when combined with a corticosteroid and to determine whether this increased efficacy is maintained over three chemotherapy courses. One hundred and two patients receiving their first course of cisplatin (50-120 mg m-2)-containing chemotherapy were randomised to receive one of the two following treatments: 8 mg OND i.v. injection and 120 mg MPD i.v. injection before chemotherapy, followed 8-12 h later by an 8 mg OND tablet and a 16 mg MPD tablet (oral treatment administered twice daily for 3-5 days): or 8 mg OND plus placebo i.v. injection before chemotherapy, followed by 8-12 h later by an 8 mg OND tablet and placebo p.o. (oral treatment administered twice daily for 3-5 days). The number of emetic episodes (EEs = vomits + retches) and the grade of nausea were recorded. Of the 101 patients studied (efficacy analysis), complete or major control (0-2 EEs) was experienced in 90.4% of patients in the first 24 h in the OND/MPD group compared with 71.4% of patients in the OND group during the first course. This difference in favour of OND/MPD was noted over the three courses and is statistically significant. In the control of delayed emesis (worst day between days 2 and 6) there is a trend in favour of the OND/MDP group during the first course [56.2% vs 43.2% for complete response (no emetic episodes)] which was statistically significant on courses 2 and 3. The global antiemetic control over the course was always in favour of OND/MPD, which leads to a better efficacy maintained over the three courses. Both treatments were well tolerated. The results of this study confirm the increased antimetic efficacy of ondansetron and methylprednisolone in combination in cisplatin-induced acute and delayed emesis which led to a better maintained efficacy over three repeated chemotherapy courses.
开展这项双盲多中心研究是为了证实昂丹司琼与皮质类固醇联合使用时其止吐疗效是否提高,并确定这种增强的疗效在三个化疗疗程中是否能持续保持。102例接受含顺铂(50 - 120 mg/m²)的首个化疗疗程的患者被随机分配接受以下两种治疗之一:化疗前静脉注射8 mg昂丹司琼和静脉注射120 mg甲泼尼龙,8 - 12小时后口服8 mg昂丹司琼片和16 mg甲泼尼龙片(口服治疗,每日两次,持续3 - 5天);或化疗前静脉注射8 mg昂丹司琼加安慰剂,8 - 12小时后口服8 mg昂丹司琼片和口服安慰剂(口服治疗,每日两次,持续3 - 5天)。记录呕吐发作次数(EEs = 呕吐 + 干呕)和恶心程度。在101例研究患者(疗效分析)中,昂丹司琼/甲泼尼龙组90.4%的患者在首个疗程的头24小时内达到完全或主要控制(0 - 2次EEs),而昂丹司琼组在首个疗程中这一比例为71.4%。在三个疗程中均观察到有利于昂丹司琼/甲泼尼龙组的这种差异,且具有统计学意义。在控制迟发性呕吐(第2至6天中最严重的一天)方面,首个疗程中存在有利于昂丹司琼/甲泼尼龙组的趋势[完全缓解(无呕吐发作)的比例分别为56.2%和43.2%],在第2和第3个疗程中具有统计学意义。整个疗程的总体止吐控制始终有利于昂丹司琼/甲泼尼龙组,这导致在三个疗程中疗效得到更好维持。两种治疗的耐受性均良好。本研究结果证实了昂丹司琼和甲泼尼龙联合使用在顺铂诱导的急性和迟发性呕吐中具有增强的止吐疗效,这使得在三个重复化疗疗程中疗效得到更好维持。