Long‐term endoscopic surveillance in HBV compensated cirrhotic patients treated with Tenofovir or Entecavir for 11 years

Author:

Farina Elisa1ORCID,Loglio Alessandro1ORCID,Tosetti Giulia1ORCID,Degasperi Elisabetta1ORCID,Viganò Mauro2,Gentile Carmine23,Monico Sara1,Perbellini Riccardo1,Borghi Marta1,Facchetti Floriana1,Uceda Renteria Sara Colonia4ORCID,Ceriotti Ferruccio4,Cerini Federica2ORCID,Primignani Massimo1,Lampertico Pietro13ORCID

Affiliation:

1. Division of Gastroenterology and Hepatology Foundation IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milan Italy

2. Division of Hepatology San Giuseppe Hospital Milan Italy

3. Department of Pathophysiology and Transplantation CRC “A. M. and A. Migliavacca” Center for Liver Disease, University of Milan Milan Italy

4. Virology Unit Foundation IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milan Italy

Abstract

SummaryBackgroundLong‐term administration of TDF/ETV in patients with HBV‐related compensated cirrhosis reduces HCC and decompensation events but the effect of this regimen on development/regression of oesophageal varices (EV) is currently unknown.AimTo assess the risk of EV development/progression in this population.MethodsA total of 186 Caucasian HBV‐monoinfected compensated cirrhotics were enrolled in a long‐term cohort study from TDF/ETV introduction. Upper GI endoscopies were performed according to Baveno recommendations. Primary endpoint was development/progression of oesophageal/gastric varices over time.ResultsAt TDF/ETV start, median age was 61 years, 80% males, 60% HBV‐DNA undetectable, 63% NUCs previously exposed, 73% normal ALT, 40% platelets <150,000/mmc and 25 (13%) with low‐risk varices (LRV). During 11 years of antiviral therapy and 666 endoscopies performed, 9 patients either developed or had a progression of oesophageal or gastric varices with an 11‐year cumulative probability of 5.1% (95% CI 3–10%); no patient bled. Out of 161 patients without EV at baseline, the 11‐year probably was 4.5% with all varices developing within the first six years of treatment. In 25 patients with LRV at baseline, the 11‐year probability of progression or regression was 9.3% and 58%, respectively. Only baseline platelet count (HR 0.96, p = 0.028) was associated with LRV development at multivariate analysis: platelet ≤90,000/mmc (AUROC 0.70) had 98.1% specificity, 42.9% sensitivity, 50% PPV for LRV onset.ConclusionsIn compensated cirrhotic patients under long‐term effective TDF/ETV treatment, the 11‐year risk of developing/progressing EV is negligible, thus challenging the current endoscopic surveillance recommendations in patients without EV at baseline.

Funder

Ministero della Salute

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

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