Laboratory of Experimental Surgery and Surgical Research N.S. Christeas, Athens University Medical School, National and Kapodistrian University of Athens, Athens, Greece,
2nd Department of Propedeutic Surgery, "Laikon" General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Dig Dis. 2020;38(4):320-328. doi: 10.1159/000503559. Epub 2019 Oct 2.
Refractory ascites represents a significant complication of decompensated cirrhosis, associated with increased mortality rates. The aim of this meta-analysis was to evaluate whether response to treatment with tolvaptan is associated with improved overall survival in cirrhotic patients with refractory ascites.
Medline, Scopus, Cochrane Central Register of Controlled Trials, Clinicaltrials.gov, and Google Scholar databases were systematically searched from inception to April 11, 2019. All studies that assessed the overall survival of patients with ascites depending on their response to tolvaptan were held eligible.
Nine studies were included, with a total of 736 patients with cirrhosis and ascites. Response to tolvaptan was estimated to be linked to significantly improved overall survival (hazard ratio [HR] 0.42, 95% CI [0.31-0.58]). Subgroup analysis indicated that the same outcome was present when tolvaptan responsiveness was defined either as effective body weight loss (HR 0.44, 95% CI [0.30-0.63] or as effective sodium restoration (HR 0.35, 95% CI [0.20-0.61]. Sensitivity analysis suggested that the presence of hepatocellular carcinoma, the sample size, and the quality of the studies did not significantly affect the overall result of the meta-analysis.
The outcomes of the meta-analysis support the prognostic role of tolvaptan response in patients with cirrhosis and refractory ascites, as it was shown to lead to significantly improved overall survival. These findings should be confirmed by future large-scale studies, while efficient biomarkers should be identified in order to accurately predict response to tolvaptan and discriminate patients that would benefit from its administration.
难治性腹水是失代偿性肝硬化的一种严重并发症,与死亡率增加有关。本荟萃分析的目的是评估托伐普坦治疗反应是否与肝硬化伴难治性腹水患者的总生存率提高相关。
系统检索了 Medline、Scopus、Cochrane 对照试验中心注册库、Clinicaltrials.gov 和 Google Scholar 数据库,检索时间截至 2019 年 4 月 11 日。所有评估腹水患者总生存率取决于其对托伐普坦反应的研究均符合入选标准。
共纳入 9 项研究,总计 736 例肝硬化伴腹水患者。托伐普坦治疗反应被估计与总生存率显著提高相关(风险比 [HR] 0.42,95%可信区间 [0.31-0.58])。亚组分析表明,当托伐普坦的反应定义为有效体重减轻(HR 0.44,95%可信区间 [0.30-0.63])或有效钠恢复(HR 0.35,95%可信区间 [0.20-0.61])时,也存在相同的结果。敏感性分析表明,肝癌的存在、样本量和研究质量均未显著影响荟萃分析的总体结果。
荟萃分析的结果支持托伐普坦反应在肝硬化伴难治性腹水患者中的预后作用,因为它显示出显著提高总生存率。这些发现应通过未来的大规模研究得到证实,同时应确定有效的生物标志物,以便准确预测对托伐普坦的反应,并区分从其治疗中获益的患者。