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Bibliographic Details
Main Authors: Matheus Souza, Lubna Al‐Sharif, Vanio L. J. Antunes, Shi Yin Wong, Daniel Q. Huang, Rohit Loomba
Format: Artículo Open Access
Published: Wiley 2026
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Online Access:https://onlinelibrary.wiley.com/doi/10.1111/apt.70565
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  • Network Meta‐Analysis: Comparison of Pharmacological Therapies in Compensated Metabolic Dysfunction‐Associated Steatohepatitis Cirrhosis for Fibrosis Regression and MASH Resolution Matheus Souza Lubna Al‐Sharif Vanio L. J. Antunes Shi Yin Wong Daniel Q. Huang Rohit Loomba Alimentary Pharmacology & Therapeutics ABSTRACT Background and Aims The burden of metabolic dysfunction‐associated steatohepatitis (MASH) cirrhosis is rapidly rising globally. There are several therapeutic agents under clinical development for the treatment of cirrhosis due to MASH; however, their relative efficacy has not been systematically assessed. This systematic review and network meta‐analysis was performed to compare the histological efficacy of available therapeutic agents for compensated MASH cirrhosis. Methods PubMed and Cochrane Library databases were searched from inception to May 25, 2025, for randomised controlled trials (RCTs) evaluating pharmacological treatments in patients with biopsy‐proven compensated MASH cirrhosis (F4c). The primary endpoint was fibrosis regression of at least one stage without MASH worsening, and the secondary endpoint was MASH resolution. Treatment comparisons were conducted via network meta‐analysis, and ranking probabilities were estimated using the surface under the cumulative ranking (SUCRA) curve analysis. Results Nine RCTs with 3266 participants met the eligibility criteria. Efruxifermin was the only intervention significantly superior to placebo for ≥ 1‐stage fibrosis improvement without worsening of MASH. The highest‐ranked interventions for fibrosis improvement were efruxifermin (SUCRA: 77.44), cilofexor + firsocostat (SUCRA: 72.38) and aldafermin (SUCRA: 71.27). For MASH resolution, efruxifermin, semaglutide + cilofexor + firsocostat and semaglutide were significantly superior to placebo. Efruxifermin (SUCRA: 81.38), semaglutide + cilofexor + firsocostat (SUCRA: 74.07) and semaglutide (SUCRA: 63.88) had the highest probability of ranking best for MASH resolution. Conclusion This network meta‐analysis provides relative rank‐order estimates of the histological efficacy of available pharmacological therapies for compensated MASH cirrhosis. These data may have implications for the design of future clinical trials. 10.1111/apt.70565 http://onlinelibrary.wiley.com/termsAndConditions#vor