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帕洛诺司琼联合 3 天阿瑞匹坦和地塞米松预防高致吐性化疗患者的恶心和呕吐。

Palonosetron plus 3-day aprepitant and dexamethasone to prevent nausea and vomiting in patients receiving highly emetogenic chemotherapy.

机构信息

Department of Clinical Oncology A, Sapienza University of Rome, Policlinico Umberto Primo, Rome, Italy.

出版信息

Support Care Cancer. 2011 Aug;19(8):1159-64. doi: 10.1007/s00520-010-0930-x. Epub 2010 Jun 16.

Abstract

BACKGROUND

The combination of a neurokinin-1 receptor antagonist, dexamethasone, and a 5-HT(3) receptor antagonist is currently the standard antiemetic treatment in patients receiving cisplatin-based high emetogenic chemotherapy (HEC). The aim of this study was to evaluate the efficacy of a combination of palonosetron, a unique second-generation 5-HT(3) receptor antagonist, aprepitant, the only approved neurokinin-1 receptor antagonist, and dexamethasone as antiemetic prophylaxis in patients receiving HEC (cisplatin ≥50 mg/mq).

METHODS

Chemotherapy-naïve adult patients, receiving cisplatin-based HEC, were treated with palonosetron 0.25 mg/i.v., dexamethasone 20 mg/i.v., and aprepitant 125 mg/p.o., 1-h before chemotherapy. Aprepitant 80 mg/p.o. and dexamethasone 4 mg p.o. were administered on days 2-3. Primary end point was complete response (CR; no vomiting and no use of rescue medication), during the overall study period (0-120 h). Secondary end points were complete control (CR and no more than mild nausea), emesis-free rate, and nausea-free rate during the acute (0-24 h), delayed (24-120 h), and overall (0-120 h) periods. Safety was also evaluated.

RESULTS

A total of 222 patients were included in the study. Median age was 62 years, 76.6% were male and 23.4% female, and most common tumors were lung (66.7%) and head and neck (15.8%); 70.3% of patients achieved CR during the overall study period. Complete control, emesis-free rate, and nausea-free rate were 70.3%, 92.8%, and 59.9%, respectively, during the overall phase. The most commonly reported side effects were constipation (39% of patients) and headache (5%).

CONCLUSIONS

This study shows that palonosetron in combination with aprepitant and dexamethasone is effective to prevent chemotherapy-induced nausea and vomiting in patients treated with cisplatin-based HEC.

摘要

背景

目前,对于接受顺铂为基础的高致吐性化疗(HEC)的患者,神经激肽-1 受体拮抗剂、地塞米松与 5-HT3 受体拮抗剂的联合应用是标准的止吐治疗方法。本研究旨在评估帕洛诺司琼(唯一的第二代 5-HT3 受体拮抗剂)、阿瑞匹坦(唯一批准的神经激肽-1 受体拮抗剂)与地塞米松联合应用作为预防接受 HEC(顺铂≥50mg/mq)的患者发生化疗诱导性恶心和呕吐(CINV)的止吐效果。

方法

本研究纳入了接受顺铂为基础的 HEC 治疗且未接受过化疗的成年患者,在化疗前 1 小时静脉内给予帕洛诺司琼 0.25mg、地塞米松 20mg,口服阿瑞匹坦 125mg。化疗后第 2-3 天,患者口服阿瑞匹坦 80mg 和地塞米松 4mg。主要终点为整个研究期间(0-120 小时)的完全缓解(无呕吐且无解救药物使用)。次要终点包括急性(0-24 小时)、延迟(24-120 小时)和整个(0-120 小时)期间的完全控制(完全缓解和恶心程度不超过轻度)、无呕吐率和无恶心率。安全性也进行了评估。

结果

共有 222 例患者入组本研究。患者的中位年龄为 62 岁,76.6%为男性,23.4%为女性,最常见的肿瘤为肺癌(66.7%)和头颈部肿瘤(15.8%);70.3%的患者在整个研究期间达到完全缓解。完全控制、无呕吐率和无恶心率在整个阶段分别为 70.3%、92.8%和 59.9%。最常见的不良反应为便秘(39%的患者)和头痛(5%)。

结论

本研究表明,帕洛诺司琼联合阿瑞匹坦和地塞米松可有效预防接受顺铂为基础的 HEC 治疗的患者发生化疗诱导性恶心和呕吐。

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