Noninvasive Assessment of Fibrosis Regression after Direct-acting Antiviral Treatment in Hepatitis C Virus Patients.


Journal

The Israel Medical Association journal : IMAJ
ISSN: 1565-1088
Titre abrégé: Isr Med Assoc J
Pays: Israel
ID NLM: 100930740

Informations de publication

Date de publication:
Dec 2021
Historique:
entrez: 26 12 2021
pubmed: 27 12 2021
medline: 5 1 2022
Statut: ppublish

Résumé

New direct acting antiviral agent (DAA) therapies are associated with a high sustained virological response rate (SVR) in hepatitis C virus (HCV) patients. The understanding of the impact of SVR on fibrosis stage is limited. To determine the effect of treatment with the DAAs on long-term liver fibrosis stages, as determined by shear-wave elastography (SWE) or FibroTest. Fibrosis stage was determined at baseline and at 6-month intervals after end of treatment (EOT), using two-dimensional SWE or FibroTest©; APRI and FIB-4 scores. The study comprised 133 SVR12 patients. After a median follow-up of 15 months (range 6-33), liver fibrosis stage decreased by at least 1 stage in 75/133 patients (56%). Cirrhosis reversal was observed in 24/82 (29%). Repeated median liver stiffness SWE values in cirrhotic patients were 15.1 kPa at baseline (range 10.5-100), 13.4 kPa (range 5.5-51) at 6 months, and 11.4 kPa (range 6.1-35.8) at 12 months after EOT, P = 0.01. During the second year after EOT, no statistically significant differences in liver fibrosis stage in 12, 18, and 24 months were found. Splenomegaly was the only significant negative predictor of liver fibrosis regression during all time points of repetitive noninvasive assessment. Following successful DAA treatment, the majority of our HCV patients with advanced fibrosis demonstrated significant improvement, as assessed by non-invasive methods. Advanced fibrosis stage was a negative predictor of fibrosis regression. Longer follow-up periods are required to further establish the impact of DAAs treatment in HCV patients with advanced fibrosis.

Sections du résumé

BACKGROUND BACKGROUND
New direct acting antiviral agent (DAA) therapies are associated with a high sustained virological response rate (SVR) in hepatitis C virus (HCV) patients. The understanding of the impact of SVR on fibrosis stage is limited.
OBJECTIVES OBJECTIVE
To determine the effect of treatment with the DAAs on long-term liver fibrosis stages, as determined by shear-wave elastography (SWE) or FibroTest.
METHODS METHODS
Fibrosis stage was determined at baseline and at 6-month intervals after end of treatment (EOT), using two-dimensional SWE or FibroTest©; APRI and FIB-4 scores.
RESULTS RESULTS
The study comprised 133 SVR12 patients. After a median follow-up of 15 months (range 6-33), liver fibrosis stage decreased by at least 1 stage in 75/133 patients (56%). Cirrhosis reversal was observed in 24/82 (29%). Repeated median liver stiffness SWE values in cirrhotic patients were 15.1 kPa at baseline (range 10.5-100), 13.4 kPa (range 5.5-51) at 6 months, and 11.4 kPa (range 6.1-35.8) at 12 months after EOT, P = 0.01. During the second year after EOT, no statistically significant differences in liver fibrosis stage in 12, 18, and 24 months were found. Splenomegaly was the only significant negative predictor of liver fibrosis regression during all time points of repetitive noninvasive assessment.
CONCLUSIONS CONCLUSIONS
Following successful DAA treatment, the majority of our HCV patients with advanced fibrosis demonstrated significant improvement, as assessed by non-invasive methods. Advanced fibrosis stage was a negative predictor of fibrosis regression. Longer follow-up periods are required to further establish the impact of DAAs treatment in HCV patients with advanced fibrosis.

Identifiants

pubmed: 34954919

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

794-800

Auteurs

Yana Davidov (Y)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Yael Inbar (Y)

Department of Radiology, Sheba Medical Center, Tel Hashomer, Israel.

Oranit Cohen-Ezra (O)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Ella Veitsman (E)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Peretz Weiss (P)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Mariya Likhter (M)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Tania Berdichevski (T)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Sima Katsherginsky (S)

Department of Radiology, Sheba Medical Center, Tel Hashomer, Israel.

Avishag Hassid (A)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Keren Tsaraf (K)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Dana Silverberg (D)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.

Ziv Ben Ari (Z)

Liver Diseases Center, Sheba Medical Center, Tel Hashomer, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

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