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首页> 外文期刊>Journal of oncology pharmacy practice: official publication of the International Society of Oncology Pharmacy Practitioners >Efficacy of aprepitant in patients receiving high-dose chemotherapy with hematopoietic stem cell support.
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Efficacy of aprepitant in patients receiving high-dose chemotherapy with hematopoietic stem cell support.

机译:阿瑞匹坦在接受大剂量化疗和造血干细胞支持的患者中的疗效。

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PURPOSE: This study describes the efficacy of aprepitant in preventing nausea and vomiting associated with high-dose chemotherapy in hematopoietic stem cell transplant (HSCT) patients. Our hypothesis is the addition of aprepitant to 5-HT3 antagonists and dexamethasone would result in a 20% increase in complete response (CR) rates compared to CR rates from published studies evaluating antiemetic regimens without aprepitant. METHODS: Adult HSCT patients receiving high-dose chemotherapy and aprepitant as part of their antiemetic regimen were included following written informed consent. CR was defined as no emesis, none to mild nausea, and no breakthrough antiemetic use. Daily patient diaries were used on days 1 through 7 following high-dose chemotherapy to collect severity of nausea, emetic episodes, breakthrough antiemetic use, and any antiemetic related side effects. RESULTS: We accrued a total of 42 patients. CR rates ranged from 42.9% to 73.8% for the 7 days. The average CR rate for days 1 through 7 was 54%. Fourteen patients (33%) maintained a complete emetic response on each of the 7 days. The average CR rate for published studies in HSCT patients receiving an antiemetic regimen without aprepitant is 57%. Most common adverse effects reported by patients receiving aprepitant were hiccups (33%) and drowsiness (33%). CONCLUSIONS: The addition of aprepitant failed to meet our primary endpoint of increasing CR rates by 20%. The lower than expected CR rate was attributed to use of breakthrough antiemetics. Aprepitant did result in preventing emesis in the majority of patients and was associated with minimal side effects.
机译:目的:本研究描述了阿瑞匹坦在预防造血干细胞移植(HSCT)患者大剂量化疗相关的恶心和呕吐中的功效。我们的假设是在5-HT3拮抗剂中添加阿瑞匹坦,而地塞米松与评估无阿瑞匹坦止吐方案的已发表研究的CR率相比,会导致完全缓解(CR)率增加20%。方法:在书面知情同意后,纳入接受大剂量化疗和阿瑞吡坦作为止吐方案一部分的成年HSCT患者。 CR被定义为没有呕吐,没有轻度恶心,也没有突破性的止吐药使用。大剂量化疗后第1至7天每天使用患者日记,以收集恶心,呕吐发作,止吐突破性使用以及止吐相关副作用的严重程度。结果:我们共计42例患者。 7天的CR率从42.9%到73.8%。第1天到第7天的平均CR率为54%。在这7天的每一天中,有14位患者(33%)保持了完全的催吐反应。接受止吐方案但无阿瑞匹坦的HSCT患者的已发表研究的平均CR率为57%。报告服用阿瑞吡坦的患者最常见的不良反应是打ic(33%)和嗜睡(33%)。结论:添加阿瑞匹坦未能达到将CR率提高20%的主要终点。 CR率低于预期是由于使用了突破性止吐药。阿瑞匹坦确实能在大多数患者中预防呕吐,并且副作用最小。

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