首页> 外文期刊>Journal of the Egyptian National Cancer Institute >Addition of 3-day aprepitant to ondansetron and dexamethasone for prophylaxis of chemotherapy-induced nausea and vomiting among patients with diffuse large B cell lymphoma receiving 5-day cisplatin-based chemotherapy
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Addition of 3-day aprepitant to ondansetron and dexamethasone for prophylaxis of chemotherapy-induced nausea and vomiting among patients with diffuse large B cell lymphoma receiving 5-day cisplatin-based chemotherapy

机译:在恩丹西酮和地塞米松基础上加用3天的阿瑞匹坦预防5天以顺铂为基础的化疗的弥漫性大B细胞淋巴瘤患者化疗引起的恶心和呕吐

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Background: Neurokinin-1 receptor antagonists, such as aprepitant are currently emerging as powerful prophylactic agents for chemotherapy-induced nausea and vomiting (CINV). Therefore, it is important to adjust the anti-emetic regimens based on personal risk factors of the patient, duration of the chemotherapy regimen and cost-effectiveness. Purpose: To determine the efficacy of the 3-day aprepitant along with ondansetron and dexamethasone in controlling CINV in patients with large B cell lymphoma receiving multiday-cisplatin regimen chemotherapy. Methods: This is a pilot prospective cross-over trial. Patients were allocated to either aprepitant 125mg on day 1 and 80mg on days 2 & 3 or placebo in the first 2 cycles, with crossover to the opposite treatment in the 3rd and 4th cycles. The primary end point was complete response (CR) of both acute (days 1-5) and delayed (days 6-8) CINV. CR means neither to develop emetic episodes nor to use rescue anti-emetics medication. Results: Twelve of the 15 patients recruited for the study were fully evaluable and completed 4 cycles of ESHAP regimen with a total of 48 cycles given. In the cycles with aprepitant and those without the CR were 83.3% and 0% respectively (p<0.05). Patients receiving aprepitant in the first 2 cycles recorded less nausea in subsequent cycles that were given without aprepitant. This was not statistically significant. Conclusion: This triple anti-emetic regimen showed efficacy in controlling the multi-day cisplatin-induced nausea and vomiting. Further randomized controlled trials are needed to compare between 3-day and 7-day aprepitant for multi-day cisplatin regimens.
机译:背景:神经激肽-1受体拮抗剂(如阿瑞匹坦)目前正在作为化学疗法引起的恶心和呕吐(CINV)的强大预防剂。因此,重要的是根据患者的个人危险因素,化疗方案的持续时间和成本效益来调整止吐方案。目的:确定为期3天的阿瑞吡坦,恩丹西酮和地塞米松在接受多日顺铂方案化疗的大B细胞淋巴瘤患者中控制CINV的疗效。方法:这是一项前瞻性交叉试验。患者在第1天和第2天分别分配阿瑞吡特125mg和第2天和第3天80mg或安慰剂,并在第3和第4个周期交叉使用相反的治疗方法。主要终点是急性(1-5天)和延迟(6-8天)CINV的完全缓解(CR)。 CR既不意味着出现催吐现象,也不使用急救止吐药物。结果:招募的15名患者中有12名是完全可评估的,并完成了4个周期的ESHAP方案,总共进行了48个周期。在具有阿瑞吡坦的循环和没有CR的循环中,分别为83.3%和0%(p <0.05)。在前两个周期中接受阿瑞吡非治疗的患者,在随后的未给予阿瑞哌非治疗的周期中,恶心较少。这没有统计学意义。结论:该三联止吐方案在控制多日顺铂引起的恶心和呕吐方面显示出功效。需要进行进一步的随机对照试验,以比较3天和7天的阿瑞匹坦治疗多天的顺铂方案。

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