These proceedings of the PHC 2019 reflect the remarkable recent advances in all fields of hepatology that are covered during this conference.Thirty years after the discovery of the hepatitis C virus (HCV), we can tell our patients that they have almost a 100% chance of cure with pangenotypic DAAs. The rare patients who relapse with resistanceassociated substitutions after DAAs therapy are cured with appropriate retreatment. Cure means eradication of HCV infection with improved quality of life and outcome. Although the WHO HCV program, which seeks the elimination of hepatitis C by 2030 may be difficult to achieve, it is accompanied by active national programs worldwide.We can tell our patients with hepatitis B that they have a 100% chance of viral suppression. Long term studies of patients receiving last generation NUCs demonstrate sustained remission without resistance, regression of liver lesions and improved outcome. WHO has set priorities to achieve global goals including more effective vaccination and easy access to therapy programs. The next objective is a cure. This objective becomes realistic with the development of effective drugs of different viral targets. Future treatment will certainly include combinations that are adapted to the different phases of hepatitis B. Patients with hepatitis delta can be told that new treatments are on the way. Ongoing phase 3 trials of Myrcludex and Lonafarnib should confirm their efficacy, which is synergistic in combination with interferon.Patients with NAFLD must be receiving counselling. However, in this emerging liver disease, which affects 25% of the population, | 2421 ABSTRACT life style counselling is only effective in a minority of patients. As we learned from NANB hepatitis before discovering the HCV, our lack of knowledge explains the problems we now face with NAFLD.The key issue is differentiating NASH from simple steatosis. There is An alternative option is the combination of SOF plus GLE/ PIB ± RBV for 12-16 weeks. Moreover, triple FDC is recommended either in combination with weight-based dose RBV and/ or to extend treatment to 16 or 14 weeks in very difficult-to-cure patients with NS5A RASs who have failed to achieve SVR twice after several DAAs regimens including protease and/or N5A inhibitors.
SUMMARYIn conclusion, the single pill triple FDC SOF/VEL/VOX for 12 weeks or the triple combination SOF plus GLE/PIB with or without ribavirin for 12 weeks achieves a 96% SVR rate in the few patients who fail DAAs combinations, even the most recent pangenotypic regimens.Therefore, with the current available rescue regimens, DAAs treatment failure is no longer significant issue.