Huc P, Block S, Carlier D, Darloy F, Bonneterre M E, Bleuse J P, Fournier C, Bonneterre J
Département d'oncologie médicale, Centre Oscar-Lambret, Lille.
Bull Cancer. 1998 Jun;85(6):562-8.
It is a randomised cross-over multicenter study comparing the efficacy and the tolerance of granisetron (Gra) 1 mg and ondansetron (Ond) 8 mg, oral, given during two consecutive cycles to 188 naive patients scheduled to receive a moderately emetogenic chemotherapy. The antiemetic treatment is given one day per course, 1 hour before chemotherapy and the second administration from 8 to 12 hours after the beginning, during each of the two cycles; alternatively according to the randomisation. Five criteria are assessed; nausea (ordinal and visual analogic scales), emeric episodes (vomiting orland retching), complete response (minor or no nausea, no emetic episode and no rescue treatment), patient preference and tolerance. The intent to treat analysis showed no significant difference at cycle 1 between Gra and Ond; at cycle 2, there is no significant difference in the number of emetic episodes; for the prevention of nausea, the ordinal scale shows a significant difference (p = 0.028 in favour of Gra at day 1 (D1) but not from D2 to D5. Gra induced more complete response than Ond at D1 (p = 0.028), but not from D2 to D5. The cross-over study did not show any period or order effect, whereas a treatment effect on Ond was significant in favour of Gra (p = 0.01). There is no significant patients preference in favour of Gra or Ond. In conclusion, Gra was more efficient in preventing nausea and obtaining complete response on the first day of treatment, significantly at the second cycle. Both Gra and Ond had a good antiemetic activity for moderately emetogenic chemotherapy with complete response rates always over 50% on day 1; delayed emesis remain less weli controlled.
这是一项随机交叉多中心研究,比较了1毫克格拉司琼(Gra)和8毫克昂丹司琼(Ond)口服给药的疗效和耐受性。在两个连续周期内,将这两种药物给予188例计划接受中度致吐性化疗的初治患者。每个疗程的止吐治疗在化疗前1小时给药1天,在两个周期的每个周期中,第二次给药在开始化疗后8至12小时;给药方式根据随机分组确定。评估了五个标准:恶心(序贯量表和视觉模拟量表)、呕吐发作(呕吐或干呕)、完全缓解(轻微恶心或无恶心、无呕吐发作且无需急救治疗)、患者偏好和耐受性。意向性分析显示,在第1周期,Gra和Ond之间无显著差异;在第2周期,呕吐发作次数无显著差异;对于恶心的预防,序贯量表显示有显著差异(第1天(D1)时p = 0.028,支持Gra,但从D2到D5时无差异)。在D1时,Gra比Ond诱导了更多的完全缓解(p = 0.028),但从D2到D5时无差异。交叉研究未显示任何周期或顺序效应,而对Ond的治疗效果显著支持Gra(p = 0.01)。患者对Gra或Ond没有显著的偏好。总之,Gra在治疗的第一天预防恶心和获得完全缓解方面更有效,在第二周期时差异显著。Gra和Ond对中度致吐性化疗均具有良好的止吐活性,第1天的完全缓解率始终超过50%;延迟性呕吐的控制效果仍然较差。