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Sa1524 — 2020 AASLD FACTORS THAT MAY AFFECT THE CHANGES OF LIVER STIFFNESS MEASUREMENTS ASSESSED BY TRANSIENT ELASTOGRAPHY (TE) IN PATIENTS WITH CHRONIC HEPATITIS B (CHB) ON LONG-TERM THERAPY WITH TENOFOVIR DISOPROXIL FUMARATE (TDF).
Liver Diseases and Transplantation
I04 Therapeutics - Approved Agents
Presented on Saturday, May 2, 2020 12:30 PM
Author(s): Hariklia Kranidioti1, Adonis A. Protopapas2, Theodoros Voulgaris3, Chrisostomos Tsolias4, PINELOPI ANTONAKAKI1, Ioanna Segkou1, Melanie Deutsch1, Christos Triantos4, John Goulis2, George Papatheodoridis3, Spilios Manolakopoulos1,3
Background and Aim
Virological remission in CHB patients on long-term TDF monotherapy is associated with an improvement in histology. The aim of this study was to evaluate the fibrosis changes as assessed by TE in a cohort of patients with CHB receiving TDF monotherapy.
Methods
We included CHB patients from the REST-B cohort who were treated with TDF for >36 months and had at least 3 Liver Stiffness Measurements (LSM) (baseline and >2 during follow-up). Virological remission was defined by undetectable serum HBV DNA with sensitive PCR assays. Liver fibrosis was assessed with transient TE (Fibroscan®). The cut-off value for advanced fibrosis/cirrhosis was 9 kPa.
Results
In total, 107 patients were included. Mean age was 56±13 years old, 59 (55%) were males and 8 (7.5%) were HBeAg positive; median follow-up period was 79 (range: 36-127) months. Virological remission rates were 96% and 98.6%, while ALT was normal (<40 IU/L) in 87% and 90% of patients at 24 and 48 months, respectively. At baseline, 38% of the patients had at least one of the following comorbidities: hypertension, diabetes mellitus, dyslipidemia or BMI>30. Median baseline liver stiffness was 6.8 (range: 3.5-40.5) kPa; 22% of the patients had advanced fibrosis/cirrhosis (mean LSM: 16±13 kPa vs 6.3±1.3 kPa for those without advanced fibrosis). A significant higher LSM was observed in patients with comorbidities (10.7±9 vs 7±3.2 kPa, p=0.04). There was a significant reduction in mean LSM between baseline and 24, 36, 48 months and last visit (8.5±6 vs 7.9±4, 7.5±4, 7±4, 7.5±5 kPa, respectively; p<0.001). At the last visit, 20% of the patients had >3 kPa decrease in LSM compared to baseline. The mean reduction of LSM was higher in patients with than without advanced fibrosis at baseline (4.9 vs 0.5 kPa, p<0.0001). A less pronounced reduction in LSM values was observed in patients with comorbidities (baseline 10±9 vs last visit 8.5±5 kPa, p=0.07).
Conclusions
Our real world data confirmed that long-term TDF monotherapy in patients with CHB is associated with a significant reduction in liver stiffness and thus a possible improvement in liver fibrosis. The reduction in LSM was noticeable mainly in patients with advanced fibrosis. Patients with comorbidities associated with metabolic syndrome do not seem to have significant decline in LSM despite their virological response
Disclosure: H. Kranidioti: No Conflicts; A. A. Protopapas: No Conflicts; T. Voulgaris: No Conflicts; C. Tsolias: No Conflicts; P. ANTONAKAKI: No Conflicts; I. Segkou: No Conflicts; M. Deutsch: No Conflicts; C. Triantos: No Conflicts; J. Goulis: No Conflicts; G. Papatheodoridis: Abbvie: Advisory Committees or Review Panels, Speaking and Teaching, Grant/Research Support; Dicerna: Advisory Committees or Review Panels; Gilead: Advisory Committees or Review Panels, Speaking and Teaching, Grant/Research Support; Roche: Advisory Committees or Review Panels; Spring-Bank: Advisory Committees or Review Panels; S. Manolakopoulos: ABBVIE: Consulting; GILEAD: Grant/Research Support, Speaking and Teaching; GILEAD SCI: Consulting; IPSEN: Speaking and Teaching; MSD: Consulting; REGULUS: Grant/Research Support;
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