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Liver and cardiovascular mortality after hepatitis C virus eradication by DAA: Data from RESIST-HCV cohort
Vincenza Calvaruso1, Salvatore Petta1, Irene Cacciola2,3
1Gastroenterology and Hepatology Unit, Department of Health Promotion Sciences Maternal and Infantile Care, Internal Medicine and Medical Specialities, PROMISE, University of Palermo, Palermo, Italy.
Insights
Achieving sustained virologic response (SVR) with direct-acting antivirals for Hepatitis C Virus (HCV) significantly improves liver and cardiovascular survival. HCV eradication benefits patients, especially those with compensated liver disease.
Area of Science:
- Hepatology
- Virology
- Public Health
Background:
- Limited real-world data exists on Hepatitis C Virus (HCV) chronic liver disease outcomes post-Sustained Virologic Response (SVR) with direct-acting antiviral drugs (DAAs).
- The impact of HCV eradication on patient mortality remains incompletely understood.
Purpose of the Study:
- To evaluate the post-treatment survival of patients with HCV after achieving SVR with DAAs.
- To assess the predictors of liver and cardiovascular mortality in this cohort.
Main Methods:
- Analysis of the RESIST-HCV cohort (4307 patients) treated with DAAs between March 2015 and December 2016.
- Utilized proportional cause-specific hazard regression for competing risks to evaluate survival and identify mortality predictors.
- Follow-up median of 73 weeks, assessing liver and cardiovascular outcomes.
Main Results:
- 94.7% of patients achieved SVR; 5.3% remained HCV RNA-positive.
- SVR was linked to significantly decreased liver mortality (HR 0.09) and cardiovascular mortality (HR 0.07).
- Platelet count, albumin, diabetes, and chronic kidney disease were identified as significant predictors for mortality.
Conclusions:
- SVR achieved with DAAs is associated with improved liver and cardiovascular survival in HCV patients.
- HCV eradication demonstrates the most significant survival benefits in patients with compensated liver disease.
- DAA therapy offers a promising strategy for improving long-term outcomes in chronic Hepatitis C.
Abstract:
Real-world evidence on the course of Hepatitis C Virus (HCV) chronic liver disease after Sustained Virologic Response (SVR) obtained with direct-acting antiviral drugs (DAAs) are still limited, and the effects on mortality remain unclear. We evaluated the post-treatment survival of 4307 patients in the RESIST-HCV cohort (mean age 66.3 ± 11.6 years, 56.9% males, 24.7% chronic hepatitis, 66.9% Child-Pugh A cirrhosis and 8.4% Child-Pugh B cirrhosis) treated with DAAs between March 2015 and December 2016 and followed for a median of 73 weeks (range 16-152). Proportional cause-specific hazard regression for competing risks was used to evaluate the survival and to assess the predictors of liver and cardiovascular death. Overall, 94.7% of patients achieved SVR while 5.3% were HCV RNA-positive at last follow-up. Sixty-three patients (1.4%) died during the observation period. SVR was associated with a decreased risk of liver mortality (hazard ratio,HR0.09, beta -2.37, p < .001). Also, platelet count (HR 0.99, beta-0.01, p = .007) and albumin value (HR 0.26, beta -1.36 p = .001) were associated with liver mortality by competing risk analysis. SVR was associated with a reduced risk of cardiovascular mortality regardless of presence of cirrhosis (HR 0.07, beta-2.67, p < .001). Presence of diabetes (HR 3.45, beta 1.24, p = .014) and chronic kidney disease class ≥3 (HR 3.60, beta 1.28, p = 0.016) were two factors independently associated with higher risk of cardiovascular mortality. Patients with SVR to a DAA therapy have a better liver and cardiovascular survival, and the effects of HCV eradication are most evident in patients with compensated liver disease.
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