Cenicriviroc Treatment for Adults With Nonalcoholic Steatohepatitis and Fibrosis: Final Analysis of the Phase 2b CENTAUR Study

被引:281
作者
Ratziu, Vlad [1 ,2 ]
Sanyal, Arun [3 ]
Harrison, Stephen A. [4 ]
Wong, Vincent Wai-Sun [5 ]
Francque, Sven [6 ]
Goodman, Zachary [7 ]
Aithal, Guruprasad P. [8 ,9 ]
Kowdley, Kris, V [10 ]
Seyedkazemi, Star [11 ]
Fischer, Laurent [11 ]
Loomba, Rohit [12 ,13 ]
Abdelmalek, Manal F. [14 ]
Tacke, Frank [15 ,16 ]
机构
[1] Hop La Pitie Salpetriere, Paris, France
[2] Sorbonne Univ, Paris, France
[3] Virginia Commonwealth Univ, Dept Gastroenterol, Richmond, VA USA
[4] Pinnacle Clin Res, San Antonio, TX USA
[5] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Peoples R China
[6] Univ Antwerp, Antwerp Univ Hosp, Gastroenterol & Hepatol, Antwerp, Belgium
[7] Inova Fairfax Med Campus, Ctr Liver Dis, Falls Church, VA USA
[8] Nottingham Univ Hosp NHS Trust, NIHR Nottingham Biomed Res Ctr, Nottingham, England
[9] Univ Nottingham, Nottingham, England
[10] Swedish Med Ctr, Liver Care Network, Seattle, WA USA
[11] Allergan Plc, San Francisco, CA USA
[12] Univ Calif San Diego, Dept Med, Div Gastroenterol, La Jolla, CA 92093 USA
[13] Univ Calif San Diego, Dept Med, NAFLD Res Ctr, La Jolla, CA 92093 USA
[14] Duke Univ, Dept Med, Div Gastroenterol & Hepatol, Durham, NC USA
[15] Univ Hosp Aachen, Dept Med 3, Aachen, Germany
[16] Charite Univ Med Ctr Berlin, Dept Gastroenterol & Hepatol, Berlin, Germany
关键词
FATTY LIVER-DISEASE; AMERICAN ASSOCIATION; DIAGNOSIS; RECOMMENDATIONS; MORTALITY; SAFETY; BIOPSY; STAGE; RISK;
D O I
10.1002/hep.31108
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims 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. Approach and Results 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. Conclusions 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).
引用
收藏
页码:892 / 905
页数:14
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