Department of Pharmacy, Kitasato University Hospital.
Education and Research Center for Clinical Pharmacy, Showa Pharmaceutical University.
Biol Pharm Bull. 2024 Mar 25;47(3):692-697. doi: 10.1248/bpb.b23-00819. Epub 2024 Feb 28.
Existing antiemetic therapy against emetic-risk agents across malignancies 24 h post-dose in the acute period in cisplatin (CDDP)-based regimens yields a satisfactory complete response (CR) rate of ≥90%. However, the control rate after 24 h in the delayed period is unsatisfactory. This study compared the efficacy of fosnetupitant (F-NTP), a neurokinin 1 receptor antagonist, with that of fosaprepitant (F-APR) and aprepitant (APR) in the treatment of patients with cancer at high emetic risk due to chemotherapy. In this retrospective case-control study involving patients receiving cisplatin-containing regimens and neurokinin 1 receptor antagonists, patients were divided into three groups based on prophylactic antiemetic therapy: F-NTP, F-APR, and APR. The CR rate was evaluated for each period up to 168 h and further subdivided into acute (0-24 h), delayed (24-120 h), overall (0-120 h), and beyond-delayed (120-168 h) periods. Eighty-eight patients were included in the F-NTP group, 66 in the F-APR group, and 268 in the APR group. The CR rates at 0-168 and 120-168 h after cisplatin administration were significantly higher in the F-NTP group than in the F-APR and APR groups. After adjusting for confounding factors, F-NTP use was an independent factor in the multivariate analysis. Prophylactic antiemetic therapy, including F-NTP, was effective and well-tolerated during the delayed period. The efficacy of F-NTP in managing chemotherapy-induced nausea and vomiting was superior to those of F-APR and APR during the study period.
现有的针对多种恶性肿瘤中顺铂(CDDP)为基础的方案中 24 小时内呕吐风险药物的止吐治疗在急性期能达到 90%以上的完全缓解(CR)率。然而,延迟期 24 小时后的控制率并不理想。本研究比较了神经激肽 1 受体拮抗剂福沙奈普肽(F-NTP)与福沙匹坦(F-APR)和阿瑞匹坦(APR)在治疗高呕吐风险癌症患者中的疗效。在这项涉及接受含顺铂方案和神经激肽 1 受体拮抗剂的患者的回顾性病例对照研究中,患者根据预防止吐治疗分为三组:F-NTP、F-APR 和 APR。评估了每个时期直至 168 小时的 CR 率,并进一步细分为急性(0-24 小时)、延迟(24-120 小时)、总体(0-120 小时)和延迟后(120-168 小时)期。88 例患者纳入 F-NTP 组,66 例患者纳入 F-APR 组,268 例患者纳入 APR 组。在顺铂给药后 0-168 小时和 120-168 小时的 CR 率在 F-NTP 组显著高于 F-APR 和 APR 组。在调整混杂因素后,F-NTP 的使用是多变量分析中的一个独立因素。包括 F-NTP 在内的预防止吐治疗在延迟期是有效且耐受良好的。在研究期间,F-NTP 在管理化疗引起的恶心和呕吐方面的疗效优于 F-APR 和 APR。