Hôpital Pitié Salpêtrière and Sorbonne Université, Paris, France.
Department of Gastroenterology, Virginia Commonwealth University, Richmond, VA.
Hepatology. 2020 Sep;72(3):892-905. doi: 10.1002/hep.31108. Epub 2020 Jul 21.
Cenicriviroc (CVC) is a C-C chemokine receptors type 2 and 5 dual antagonist under evaluation for treating liver fibrosis in adults with nonalcoholic steatohepatitis (NASH). Year 1 primary analysis of the 2-year CENTAUR study showed that CVC had an antifibrotic effect without impacting steatohepatitis. Herein, we report the final data from year 2 exploratory analyses.
This was a randomized, controlled study of adults with NASH, nonalcoholic fatty liver disease activity score ≥4, and NASH Clinical Research Network stage 1-3 fibrosis. Participants in arms A and C received CVC 150 mg or placebo, respectively, for 2 years; arm B received placebo in year 1 and switched to CVC in year 2. Liver biopsy was performed at baseline, year 1, and year 2. Of 289 randomized participants, 242 entered year 2. At year 2, 24% of patients who switched to CVC and 17% who remained on placebo achieved ≥1-stage fibrosis improvement and no worsening of NASH (P = 0.37). Twice the proportion on CVC who achieved fibrosis response at year 1 maintained benefit at year 2 (60% arm A versus 30% arm C), including 86% on CVC who had stage 3 fibrosis at baseline. Over 2 years, a similar proportion on CVC or placebo achieved ≥1-stage fibrosis improvement and no worsening of NASH (15% arm A versus 17% arm C). In patients with fibrosis responses, we observed consistent reductions in levels of N-terminal type 3 collagen propeptide and enhanced liver fibrosis scores, while increases in aspartate aminotransferase-to-platelet ratio index and Fibrosis-4 scores were consistently observed in nonresponders. Safety profile was comparable across groups.
CVC was well tolerated, and year 2 data corroborate antifibrotic findings from year 1. The majority on CVC who achieved fibrosis response at year 1 maintained it at year 2, with greater effect in advanced fibrosis. ClinicalTrials.gov number, NCT02217475 (CENTAUR).
Cenicriviroc(CVC)是一种 C-C 趋化因子受体 2 和 5 双重拮抗剂,正在评估其用于治疗非酒精性脂肪性肝炎(NASH)成人的肝纤维化。为期 2 年的 CENTAUR 研究的第 1 年主要分析显示,CVC 具有抗纤维化作用,而不会影响脂肪性肝炎。在此,我们报告第 2 年探索性分析的最终数据。
这是一项针对 NASH、非酒精性脂肪性肝病活动评分≥4 和 NASH 临床研究网络 1-3 期纤维化的成年人的随机、对照研究。A 组和 C 组的参与者分别接受 CVC 150mg 或安慰剂,为期 2 年;B 组在第 1 年接受安慰剂,第 2 年转换为 CVC。基线、第 1 年和第 2 年进行肝活检。在 289 名随机参与者中,有 242 名进入第 2 年。在第 2 年,转换为 CVC 的患者中有 24%和继续接受安慰剂的患者中有 17%实现了≥1 期纤维化改善且无 NASH 恶化(P=0.37)。在第 1 年实现纤维化反应的 CVC 患者中,有两倍的比例在第 2 年保持获益(A 组 60%,C 组 30%),包括基线时患有 3 期纤维化的 86%的患者。在 2 年期间,CVC 或安慰剂组实现≥1 期纤维化改善且无 NASH 恶化的比例相似(A 组 15%,C 组 17%)。在纤维化反应患者中,我们观察到 N-末端 3 型胶原前肽水平持续降低和肝纤维化评分增强,而在无反应者中,天门冬氨酸氨基转移酶与血小板比值指数和纤维化 4 评分持续升高。各组的安全性特征相似。
CVC 耐受良好,第 2 年的数据证实了第 1 年的抗纤维化发现。在第 1 年实现纤维化反应的 CVC 患者中,大多数在第 2 年保持纤维化反应,在晚期纤维化中效果更大。临床试验.gov 编号,NCT02217475(CENTAUR)。