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Hepatitis C Virus Clearance in Older Adults
Antonio Massimo Ippolito1, Angelo Iacobellis1, Michele Milella2
1Division of Gastroenterology, Casa Sollievo Sofferenza Hospital, Istituto di Ricovero e Cura a Carattere Scientifico, San Giovanni Rotondo, Italy.
Insights
Older adults (80+) with Hepatitis C Virus (HCV) infection achieved high sustained viral response (SVR) rates using direct-acting antiviral (DAA) therapy. DAAs are safe and effective, with specific patient factors predicting better outcomes.
Area of Science:
- Hepatology
- Geriatric Medicine
- Infectious Diseases
Background:
- Chronic Hepatitis C Virus (HCV) infection poses significant health risks, particularly in older adult populations.
- Direct-acting antiviral (DAA) therapies have revolutionized HCV treatment, but data on very elderly individuals are limited.
- Assessing treatment efficacy and safety in adults aged 80 and above is crucial for optimizing care.
Purpose of the Study:
- To evaluate the sustained viral response (SVR) rates in individuals aged 80 and older treated with direct-acting antiviral (DAA) therapy for Hepatitis C Virus (HCV).
- To assess the safety and global clinical effect of various DAA combinations in this elderly cohort.
- To identify risk factors for adverse events in older adults undergoing DAA treatment for HCV.
Main Methods:
- A cohort of 253 participants aged 80 and older with chronic HCV infection (213 with cirrhosis, 40 with advanced fibrosis) was studied.
- Treatment efficacy and safety were investigated using different DAA combinations.
- Participants were staged using Child-Pugh-Turcotte, MELD, and D'Amico systems; comorbidities and clinical events were meticulously recorded.
Main Results:
- Ninety-five percent of participants achieved SVR, irrespective of sex, HCV genotype, or treatment schedule.
- During a mean follow-up of 14 months, 34 events occurred in 27 participants, including hepatocellular carcinoma, hepatic decompensation, nonhepatic events, and deaths.
- Multivariate analysis identified D'Amico Stages 4-5, low baseline serum albumin (<3.5 mg/dL), and ≥3 comorbidities as risk factors for adverse events.
Conclusions:
- Direct-acting antiviral (DAA) therapy is safe and effective for older adults (80+) with HCV-related advanced fibrosis or cirrhosis in a real-world setting.
- Patients with preserved albumin synthesis and fewer than three baseline comorbidities are most likely to benefit from DAA therapy.
- These findings support the use of DAAs in the elderly population, with careful consideration of individual risk factors.
Objectives:
To determine whether older adults with the hepatitis C virus (HCV) achieve a sustained viral response (SVR) after treatment with direct-acting antiviral therapy.
Participants:
Individuals aged 80 and older with chronic HCV infection (N = 253; n = 213 with cirrhosis, n = 40 with advanced fibrosis).
Measurements:
We investigated the efficacy, safety, and global clinical effect of treatment with different combinations of direct antiviral agents (DAAs). Participants with cirrhosis were staged according to Child-Pugh-Turcotte class, Model for End-Stage Liver Disease score, and the D'Amico staging system. The type and number of comorbidities at baseline and hepatic and nonhepatic events during follow-up were registered.
Results:
Ninety-five percent of participants with cirrhosis and 95% of those with advanced fibrosis attained SVR. The rate was independent of sex, HCV genotype, and treatment schedule. During a mean follow-up of 14 ± 4 months (range 5-23 months), 34 events occurred in 27 participants: 10 hepatocellular carcinomas, 12 hepatic decompensations, 9 nonhepatic events, 3 deaths. Multivariate analysis of risk factors for experiencing adverse events during follow up showed that participants in D'Amico Stages 4 and 5, with a baseline serum albumin level of 3.5 mg/dL or less, and 3 or more comorbidities were the most at risk.
Conclusion:
In a real-world setting, DAAs are safe and effective in older adults with HCV-related advanced fibrosis or cirrhosis. Individuals with preserved albumin synthesis and fewer than 3 comorbidities at baseline have the most to gain from long-term DAA therapy.
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