Primary Objective: To evaluate the long-term outcomes including liver related morbidity, mortality and hepatocellular carcinoma (HCC) development as compared to those of historical control with interferon(IFN)-based treatment. Secondary Objective: 1. To access liver fibrosis progression/regression in CHC patients after sofosbuvir-based treatment. 2. To investigate the long-term outcomes of extrahepatic manifestations of the sofosbuvir-based treated cohort as compared to their pretreatment status.
Primary Endpoint: To evaluate the long-term event-free effect after sofosbuvir-based therapy, in terms of free of major liver events (including HCC, decompensation with ascites, variceal bleeding, hepatic encephalopathy, and liver-related mortality) in CHC patients. Secondary Endpoints: 1. To evaluate hepatic fibrosis progression or regression in CHC patients after sofosbuvir-based therapy. 2. To evaluate the durability of sustained viral response (SVR) in patients achieving SVR after sofosbuvir-based therapy. 3. To evaluate long-term effect of sofosbuvir-based therapy on the extra-hepatic manifestations of the cohort. The items include mixed cryoglobulinemia, chronic kidney diseases, insulin resistance, diabetic status, cardiovascular events and dyslipidemia. 4. To evaluate long-term effect of sofosbuvir-based therapy on quality of life on the cohort. Study Design Prospective, longitudinal observational study Study procedure A total of 200 patients receiving sofosbuvir based direct antiviral agents (DAAs) in the parent studies will be included for following up to 5 years. Their serological, image study and disease status description will be prospectively documented to present the long term effects of sofosbuvir-based therapy. The presentation of illness will be specified as: 1. Main hepatic complications as liver fibrosis, hepatic malignancy, liver decompensation with ascites, hepatic encephalopathy and variceal bleeding, and liver-related mortality. 2. Life quality, extrahepatic symptoms as cryoglobulinemia, diabetes mellitus, insulin resistance, lipid profiles, renal insufficiency and other non-liver morbidities and malignancy.
Study Type
OBSERVATIONAL
Enrollment
200
Korea University Ansan Hospital
Ansan, South Korea
RECRUITINGAsan Medical Center
Asan, South Korea
RECRUITINGSoon Chun Hyang University Hospital Bucheon.
Bucheon-si, South Korea
RECRUITINGDong-A University Hospital
Busan, South Korea
RECRUITINGInje University Busan Paik Hospital
Busan, South Korea
RECRUITINGKyungpook National University Hospital
Daegu, South Korea
RECRUITINGGachon University Gil Hospital
Incheon, South Korea
RECRUITINGPusan National University Hospital
Pusan, South Korea
RECRUITINGGangnam Severance Hospital
Seoul, South Korea
RECRUITINGKorea University Guro Hospital
Seoul, South Korea
RECRUITING...and 16 more locations
Number of participants with liver-related morbidity development during 5-year follow-up period after sofosbuvir-based treatment
Number of participants with liver-related morbidity during 5-year follow-up period after sofosbuvir-based treatment, including liver fibrosis progression and decompensation
Time frame: 6 years
Number of participants with liver-related mortality development during 5-year follow-up period after sofosbuvir-based treatment
Number of participants with liver-related mortality assessed by death due to HCC and/or liver decompensation
Time frame: 6 years
Number of participants with hepatocellular carcinoma (HCC) development during 5-year follow-up period after sofosbuvir-based treatment
Number of participants with HCC assessed by histocytology or positive dynamic image plus alpha fetoprotein (AFP) \> 400 ng/ml
Time frame: 6 years
Life quality
The change of short form(SF)-36 from baseline
Time frame: 6 years
Cryoglobulinemia
Change of proportion of participants with cryoglobulinemia from baseline cryoglobulinemia from baseline)
Time frame: 6 years
Diabetes mellitus (DM)
Number of participants without DM develop DM assessed by Ac sugar \> 126 g/ml
Time frame: 6 years
Insulin resistance
Change of homeostatic model assessment (HOMA-IR), assessed by Glucose x insulin/22.5 from baseline
Time frame: 6 years
Lipid profiles
Change of the serum profile of lipids including triglyceride(TG), cholesterol(Chol), low-density lipoprotein-cholesterol (LDL-C), high-density lipoprotein-cholesterol (HDL-C) from baseline
Time frame: 6 years
Renal disease
the change of the estimated glomerular filtration rate (eGFR) from baseline
Time frame: 6 years
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