
From EASL 2026: What Hepatology Still Needs to Solve
MASH cirrhosis treatment, fibrosis reversal, and population screening were cited by experts as hepatology's biggest gaps.
Treating patients with metabolic dysfunction–associated steatohepatitis (MASH) cirrhosis, scaling population-level screening, and addressing chronically underfunded conditions top the list of hepatology's most pressing unmet needs, according to experts who presented at the
Why MASH Cirrhosis Demands the Field's Immediate Attention
Urgency around
"Finding treatment that can slow progression to decompensation is highly desirable, but even we want to take it a step further and potentially develop treatments that can lead to a reversal of MASH cirrhosis," said Alkhouri. He added that fibrosis reversal rates above 15% to 20% are achievable through more potent agents or combination regimens and could meaningfully reduce rates of liver cancer and hepatic complications.
Mazen Noureddin, MD, MHSc, professor of medicine and transplant hepatologist at Houston Methodist Hospital, drew on the
Screening Gaps, Alcohol Disease, and the Compounding Burden of Steatotic Liver Disease
Zobair M. Younossi, MD, chairman of The Global NASH/MASH Council, placed individual disease categories within a larger framework. Steatotic liver disease, which encompasses MASH, alcohol-associated liver disease, and metabolic and alcohol–related liver disease (metALD), is now the leading indication for liver transplantation in both Europe and the US. Beyond its standalone burden, steatotic liver disease acts as a compounding factor for patients with hepatitis B or hepatitis C, worsening outcomes across disease states regardless of region.
“These diseases [are] not only important by themselves, but also they're important because they aggravate any other liver disease that you have, so that the disease burden from a liver standpoint is going to be higher,” Younossi said.
Meena Bansal, MD, professor of medicine and system chief of the Division of Liver Diseases at the Icahn School of Medicine at Mount Sinai, pointed to a gap between knowledge and action: validated algorithms to screen at-risk populations for fibrosis already exist, but their deployment and impact at a population level remain largely unassessed.
Tarik Asselah, MD, PhD, professor of hepatology at Hôpital Beaujon and the University of Paris-Cité, highlighted alcohol-related liver disease and rare liver conditions as chronically underfunded areas and pointed to early-phase gene therapy research in hepatitis B as a technology worth watching.




