Pediatric Oncology Group of Ontario, Toronto, Canada.
Department of Pharmacy, The Hospital for Sick Children, Toronto, Canada.
Support Care Cancer. 2022 Nov;30(11):8855-8869. doi: 10.1007/s00520-022-07287-w. Epub 2022 Aug 12.
To identify effective and safe interventions to prevent acute phase chemotherapy-induced nausea and vomiting (CINV) in adult and pediatric patients.
We conducted a systematic review of randomized trials evaluating interventions to prevent acute CINV. Outcomes assessed were complete chemotherapy-induced vomiting (CIV) control, complete chemotherapy-induced nausea (CIN) control, complete CINV control, and discontinuation of antiemetics due to adverse effects.
The search identified 65,172 citations; 744 were evaluated at full-text, and 295 (25 pediatric) met eligibility criteria. In patients receiving highly emetogenic chemotherapy (HEC), complete CIV (risk ratio (RR) 1.23, 95% confidence interval (CI) 1.05-1.44) and CIN (RR 1.34, 95% CI 1.10-1.62) control improved when olanzapine was added. The addition of a neurokinin-1 receptor antagonist (NK1RA) to a corticosteroid plus a serotonin-3 receptor antagonist (5HT3RA) also improved complete CIV (RR 1.11, 95% CI 1.08-1.14) and CIN (RR 1.05, 95% CI 1.01-1.08) control. Compared to granisetron/ondansetron, palonosetron provided improved complete CIV control when the 5HT3RA was given alone or when combined with dexamethasone. In patients receiving moderately emetogenic chemotherapy (MEC), dexamethasone plus a 5HT3RA improved complete CIV control compared to a 5HT3RA alone (RR 1.29, 95% CI 1.21-1.39). Only a single meta-analysis evaluating the safety outcome was possible.
For patients receiving HEC, various antiemetic regimens improved CIV and CIN control. For patients receiving MEC, administration of a 5HT3RA plus dexamethasone improved CIV control. Analysis of antiemetic safety was constrained by lack of data.
确定预防成人和儿科患者化疗诱导的急性恶心和呕吐(CINV)的有效且安全的干预措施。
我们对评估预防急性 CINV 的干预措施的随机试验进行了系统评价。评估的结果是完全化疗诱导的呕吐(CIV)控制、完全化疗诱导的恶心(CIN)控制、完全 CINV 控制和因不良反应而停止止吐药。
搜索确定了 65172 个引文;744 个在全文评估,295 个(25 个儿科)符合入选标准。在接受高致吐性化疗(HEC)的患者中,当添加奥氮平时,完全 CIV(风险比(RR)1.23,95%置信区间(CI)1.05-1.44)和 CIN(RR 1.34,95%CI 1.10-1.62)控制得到改善。神经激肽-1 受体拮抗剂(NK1RA)联合皮质类固醇和 5-羟色胺-3 受体拮抗剂(5HT3RA)的添加也改善了完全 CIV(RR 1.11,95%CI 1.08-1.14)和 CIN(RR 1.05,95%CI 1.01-1.08)控制。与格拉司琼/昂丹司琼相比,当单独给予帕洛诺司琼或与地塞米松联合使用时,5HT3RA 提供了更好的完全 CIV 控制。在接受中度致吐性化疗(MEC)的患者中,与单独使用 5HT3RA 相比,地塞米松联合 5HT3RA 改善了完全 CIV 控制(RR 1.29,95%CI 1.21-1.39)。仅对一项可能的安全性结局进行了单一的荟萃分析。
对于接受 HEC 的患者,各种止吐方案改善了 CIV 和 CIN 控制。对于接受 MEC 的患者,5HT3RA 加地塞米松的给药改善了 CIV 控制。由于缺乏数据,对止吐安全性的分析受到限制。