Department of Hepato-Gastroenterology, University Hospital F. Mitterrand, Dijon, France.
Department of Hepato-Gastroenterology, University Hospital Trousseau, Tours, France.
J Hepatol. 2019 Sep;71(3):516-522. doi: 10.1016/j.jhep.2019.04.021. Epub 2019 May 22.
BACKGROUND & AIMS: Sorafenib is the standard of care for advanced hepatocellular carcinoma (HCC). Combining sorafenib with another treatment, to improve overall survival (OS) within an acceptable safety profile, might be the next step forward in the management of patients with advanced HCC. We aimed to assess whether a combination of sorafenib and a statin improved survival in patients with HCC. METHODS: The objective of the PRODIGE-11 trial was to compare the respective clinical outcomes of the sorafenib-pravastatin combination (arm A) versus sorafenib alone (arm B) in patients with advanced HCC. Child-Pugh A patients with advanced HCC who were naive to systemic treatment (n = 323) were randomly assigned to sorafenib-pravastatin combination (n = 162) or sorafenib alone (n = 161). The primary endpoint was OS; secondary endpoints were progression-free survival, time to tumor progression, time to treatment failure, safety, and quality of life. RESULTS: After randomization, 312 patients received at least 1 dose of study treatment. After a median follow-up of 35 months, 269 patients died (arm A: 135; arm B: 134) with no difference in median OS between treatments arms (10.7 months vs. 10.5 months; hazard ratio = 1.00; p = 0.975); no difference was observed in secondary survival endpoints either. In the univariate analysis, the significant prognostic factors for OS were CLIP score, performance status, and quality of life scores. The multivariate analysis showed that the only prognostic factor for OS was the CLIP score. The main toxicity was diarrhea (which was severe in 11% of patients in arm A, and 8.9% in arm B), while severe nausea-vomiting was rare, and no toxicity-related deaths were reported. CONCLUSION: Adding pravastatin to sorafenib did not improve survival in patients with advanced HCC. LAY SUMMARY: Sorafenib has proven efficacy for the treatment of patients with advanced hepatocellular carcinoma. However, overall survival remains poor in these patients, so we were interested to see if the addition of a statin, pravastatin, improved outcomes in patients with advanced HCC. This randomized-controlled trial demonstrated that the sorafenib-pravastatin combination did not improve overall survival in this study population compared to sorafenib alone. Clinical trial number: NCT01075555.
背景与目的:索拉非尼是治疗晚期肝细胞癌(HCC)的标准治疗方法。将索拉非尼与另一种治疗方法联合使用,在可接受的安全性范围内提高总生存期(OS),可能是晚期 HCC 患者管理的下一步。我们旨在评估索拉非尼和他汀类药物联合治疗是否能改善 HCC 患者的生存。
方法:PRODIGE-11 试验的目的是比较晚期 HCC 患者中索拉非尼-普伐他汀联合治疗(A 组)与索拉非尼单药治疗(B 组)的临床结果。323 例初治晚期 HCC 患者(Child-Pugh A)随机分配接受索拉非尼-普伐他汀联合治疗(n=162)或索拉非尼单药治疗(n=161)。主要终点是 OS;次要终点包括无进展生存期、肿瘤进展时间、治疗失败时间、安全性和生活质量。
结果:随机分组后,312 例患者至少接受了 1 剂研究治疗。中位随访 35 个月后,269 例患者死亡(A 组 135 例,B 组 134 例),两组 OS 无差异(10.7 个月 vs. 10.5 个月;风险比=1.00;p=0.975);次要生存终点也未见差异。单因素分析显示,OS 的显著预后因素为 CLIP 评分、体力状态和生活质量评分。多因素分析显示,OS 的唯一预后因素是 CLIP 评分。主要毒性为腹泻(A 组 11%患者严重,B 组 8.9%),严重恶心呕吐罕见,无毒性相关死亡。
结论:在晚期 HCC 患者中,加用普伐他汀不能改善索拉非尼的生存。
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