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首页> 外文期刊>BioMed research international >Phase II, Open Label, Randomized Comparative Trial of Ondansetron Alone versus the Combination of Ondansetron and Aprepitant for the Prevention of Nausea and Vomiting in Patients with Hematologic Malignancies Receiving Regimens Containing High-Dose Cytarabine
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Phase II, Open Label, Randomized Comparative Trial of Ondansetron Alone versus the Combination of Ondansetron and Aprepitant for the Prevention of Nausea and Vomiting in Patients with Hematologic Malignancies Receiving Regimens Containing High-Dose Cytarabine

机译:恩丹西酮单独与恩丹西酮和阿瑞匹坦联合用于预防接受大剂量阿糖胞苷治疗的血液系统恶性肿瘤患者的恶心和呕吐的II期,开放标签,随机比较试验

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Background. Aprepitant is a Peurokinin-1 receptor antagonist approved for the prevention of CINV in moderate emetic risk chemotherapy. We explored its effectiveness in patients with leukemia receiving cytarabine-based chemotherapy.Methods. Patients were randomized to ondansetron (OND) 8 mg IV 30 minutes before cytarabine followed by 24 mg IV continuous infusion daily until 6–12 hours after the last dose of chemotherapy alone or with aprepitant (APREP) oral 125 mg 6–12 hrs before chemotherapy and 80 mg daily until 1 day after the last dose of chemotherapy.Results. Forty-nine patients were enrolled in each arm; 42 in OND and 41 in OND + APREP arm were evaluable for efficacy. The ORR with OND + APREP was 80% compared to 67% with OND alone (P=0.11). On days 6 and 7, higher proportion of patients treated with OND + APREP were free from nausea (74%, 74% versus 68%, 67%;P=0.27and 0.18, resp.). Requirement of rescue medications on days 2 and 3 was fewer in OND + APREP arm 7% and 5% compared to 21% and 16% in the OND arm, respectively (P=0.06andP=0.07).Conclusions. There was a trend for overall improvement in emesis with ondansetron plus aprepitant. The potential benefit of this approach with specific chemotherapy combinations remains to be determined.
机译:背景。 Aprepitant是一种P /神经激肽1受体拮抗剂,已被批准用于中度催吐风险化疗中预防CINV的治疗。我们探讨了其在以阿糖胞苷为基础的化疗的白血病患者中的有效性。患者在阿糖胞苷前30分钟被随机分配到恩丹西酮(OND)静脉注射8μmg,然后每天连续静脉输注24μmg,直到最后一次单独化疗后或在化疗前6-12小时口服阿瑞哌汀(APREP)125μmg一次每天80μg,直到最后一次化疗后1天。每组招募了49名患者。 OND组中有42例,OND + APREP组中有41例可评估疗效。 OND + APREP的ORR为80%,而仅OND的ORR为67%(P = 0.11)。在第6天和第7天,接受OND + APREP治疗的患者中无恶心的比例更高(分别为74%,74%和68%,67%; P = 0.27和0.18)。 OND + APREP组在第2天和第3天的急救药物需求分别为7%和5%,而OND + APREP组分别为21%和16%(P = 0.06和P = 0.07)。恩丹西酮加阿瑞匹坦的呕吐有总体改善的趋势。这种方法与特定化学疗法组合的潜在益处尚待确定。

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