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首页> 外文期刊>The oncologist >One-Day Versus Three-Day Dexamethasone in Combination with Palonosetron for the Prevention of Chemotherapy-Induced Nausea and Vomiting: A Systematic Review and Individual Patient Data-Based Meta-Analysis
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One-Day Versus Three-Day Dexamethasone in Combination with Palonosetron for the Prevention of Chemotherapy-Induced Nausea and Vomiting: A Systematic Review and Individual Patient Data-Based Meta-Analysis

机译:为期一天与三天的地塞米松与PalonoSetron结合预防化疗诱导的恶心和呕吐:系统审查和个体患者基于患者的荟萃分析

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Background A dexamethasone-sparing regimen consisting of palonosetron plus 1-day dexamethasone for the prevention of chemotherapy-induced nausea and vomiting (CINV) has been studied previously. Here, we evaluate the noninferiority of the dexamethasone-sparing regimen in overall antiemetic control using a meta-analysis based on individual patient data (IPD). Materials and Methods We conducted a systematic review for randomized trials reporting CINV outcomes for the comparison of palonosetron plus 1-day dexamethasone (d1 arm) versus the same regimen followed by dexamethasone on days 2–3 after chemotherapy (d3 arm) in chemotherapy-na?ve adult patients undergoing either moderately emetogenic chemotherapy (MEC) or anthracycline plus cyclophosphamide (AC)-containing chemotherapy. PubMed and MEDLINE were searched electronically. A manual search was also conducted. The primary endpoint was complete response (CR; no emesis and no rescue medication) in the overall 5-day study period. The noninferiority margin was set at ?8.0% (d1 arm?d3 arm). Results Five studies ( n = 1,194) were eligible for analysis and all IPD was collected. In the overall study period, the d1 arm showed noninferiority to the d3 arm for CR as well as complete control (pooled risk difference in CR rate ? 1.5%, 95% confidence interval [CI] ?7.1 to 4.0%, I 2 = 0%; in complete control rate ? 2.4%, 95% CI ?7.7 to 2.9%, I 2 = 0%). There was no significant interaction between dexamethasone regimen and risk factors (type of chemotherapy, sex, age, and alcohol consumption). Conclusion This IPD meta-analysis indicates that the dexamethasone-sparing regimen is not associated with a significant loss in overall antiemetic control in patients undergoing MEC or AC-containing chemotherapy, irrespective of known risk factors for CINV. Implications for Practice Although dexamethasone in combination with other antiemetic agents has been used to prevent chemotherapy-induced nausea and vomiting (CINV), it is of clinical importance to minimize total dose of dexamethasone in patients undergoing multiple cycles of emetogenic chemotherapy. This individual-patient-data meta-analysis from five randomized controlled trials (1,194 patients) demonstrated a noninferiority of the dexamethasone-sparing regimen for complete response and complete control of CINV. The outcomes were comparable across patients with different characteristics. These findings thus help physicians minimize use of the steroid and further reduce the burden of dexamethasone-related side effects in patients undergoing multiple consecutive courses of emetogenic chemotherapy.
机译:背景技术先前已经研究了由Palonosetron和1天地塞米松组成的地塞塞塞松备用方案,用于预防化疗诱导的恶心和呕吐(CINV)。在这里,我们使用基于个体患者数据(IPD)的META分析来评估整个止吐控制中的地塞米松备受方案的非分析。材料和方法我们对随机试验进行了系统审查,该试验报告了CinV结果,用于比较Palonosetron加1天地塞米松(D1 ARM)与同一方案,然后在化疗 - NA中的化疗(D3臂)后2-3天2-3天中的地塞米松ve成年患者接受中等均匀化疗(MEC)或蒽环类丙氨酸加环磷酰胺(AC)化疗。被电子方式搜索PubMed和Medline。还进行了手动搜索。在整个5天的研究期间,主要终点是完全反应(CR;无呕吐和救援药物)。不合理利润率设定为?8.0%(D1 ARM?D3 ARM)。结果五项研究(N = 1,194)有资格进行分析,所有IPD都收集。在整体研究期间,D1臂向CR的D3臂显示出CR以及完全对照(CR率的汇集风险差异?1.5%,95%置信区间[CI]?7.1至4.0%,I 2 = 0 %;完全控制率?2.4%,95%CI?7.7至2.9%,I 2 = 0%)。地塞米松方案与风险因素之间没有显着的相互作用(化疗,性别,年龄和酒精消费类型)。结论该IPD荟萃分析表明,不管CINV的已知风险因素如何,地塞米松排放方案与患有MEC或AC化疗的患者的总体止吐控制无关。对实践的影响尽管地塞米松与其他止吐剂结合使用的是用于预防化疗诱导的恶心和呕吐(CINV),但在经历多种均匀化疗循环的患者中最小化地塞米松的总剂量是临床重要性。来自五种随机对照试验(1,194名患者)的这种个体患者数据荟萃分析证明了地塞米松的不合理性,用于完全反应和完全控制Cinv。在不同特征的患者中,结果是可比的。因此,这些结果有助于医生最大限度地减少对类固醇的使用,并进一步降低了在进行多个均匀化疗疗程的患者患者中的地塞米松相关副作用的负担。

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