Department of Clinical Oncology A, Sapienza University of Rome, Policlinico Umberto Primo, Rome, Italy.
Support Care Cancer. 2011 Aug;19(8):1159-64. doi: 10.1007/s00520-010-0930-x. Epub 2010 Jun 16.
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).
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.
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%).
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.
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。
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。
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%)。
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。