Division of Colon and Rectal Surgery, Department of Surgery, En Chu Kong Hospital, New Taipei City, Taiwan.
Department of Pharmacy, En Chu Kong Hospital, 399 Fuxing Road Sanxis District, New Taipei City, 23741, Taiwan.
Eur J Clin Pharmacol. 2021 Nov;77(11):1597-1609. doi: 10.1007/s00228-021-03157-2. Epub 2021 May 15.
Chemotherapy-induced nausea and vomiting (CINV) commonly occurs after chemotherapy, adversely affecting patients' quality of life. Recently, studies have shown inconsistent antiemetic effects of two common 5-hydroxytryptamine 3 receptor antagonists, namely, palonosetron and granisetron. Therefore, we conducted a meta-analysis to evaluate the effectiveness of palonosetron versus granisetron in preventing CINV.
Relevant studies were obtained from PubMed, Embase, and Cochrane databases. The primary outcome was the complete response (CR) rate. Secondary outcomes were headache and constipation events.
In total, 12 randomized controlled trials and five retrospective studies were reviewed. Palonosetron was consistently statistically superior to granisetron in all phases in terms of the CR rate (acute phases: odds ratio [OR] = 1.28, 95% confidence interval [CI] = 1.06-1.54; delayed phases: OR = 1.38, 95% CI = 1.13-1.69; and overall phases: OR = 1.37, 95% CI = 1.17-1.60). Moreover, a non-significant difference was found between the two groups in terms of the headache event, but the occurrence of the constipation event was lower in the granisetron group than in the palonosetron group.
Palonosetron showed a higher protective efficacy in all phases of CINV prevention, especially in delayed phases, and no relatively severe adverse effects were observed.
化疗引起的恶心和呕吐(CINV)在化疗后常发生,会对患者的生活质量产生不良影响。最近的研究表明,两种常见的 5-羟色胺 3 受体拮抗剂,即帕洛诺司琼和格拉司琼,在止吐方面的效果不一致。因此,我们进行了一项荟萃分析,以评估帕洛诺司琼与格拉司琼预防 CINV 的效果。
从 PubMed、Embase 和 Cochrane 数据库中获取相关研究。主要结局是完全缓解(CR)率。次要结局是头痛和便秘事件。
共回顾了 12 项随机对照试验和 5 项回顾性研究。在所有阶段,帕洛诺司琼在 CR 率方面均明显优于格拉司琼(急性期:比值比 [OR] = 1.28,95%置信区间 [CI] = 1.06-1.54;延迟期:OR = 1.38,95%CI = 1.13-1.69;总期:OR = 1.37,95%CI = 1.17-1.60)。此外,两组在头痛事件方面无显著差异,但格拉司琼组便秘事件的发生率低于帕洛诺司琼组。
帕洛诺司琼在 CINV 预防的所有阶段均表现出更高的保护效果,尤其是在延迟期,且未观察到相对严重的不良反应。