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Published on: October 29, 2015
Management of HCV-related decompensated cirrhosis with direct-acting antiviral agents: who should be treated?
Amr Shaaban Hanafy1,2, Mohamed A Bassiony3, Mohammad Abd Alkhalik Basha4
1Internal Medicine Department, Hepatology Division, Zagazig University, Sharkia, Zagazig, 44519, Egypt. Dr_amr_hanafy@yahoo.com.
Insights
Direct-acting antiviral drugs (DAAs) significantly improved outcomes for patients with hepatitis C virus (HCV) decompensated cirrhosis. Treatment led to better liver function, reduced complications, and increased survival rates in this challenging patient group.
Area of Science:
- Hepatology
- Virology
- Clinical Medicine
Background:
- Decompensated cirrhosis due to hepatitis C virus (HCV) presents ongoing treatment challenges, even with direct-acting antiviral drugs (DAAs).
- HCV genotype 4-related decompensated cirrhosis requires effective management strategies.
- Clinical Trial NCT03547895 evaluated DAA efficacy in this population.
Purpose of the Study:
- To assess the efficacy and safety of direct-acting antiviral drugs (DAAs) in managing hepatitis C virus (HCV) genotype 4-related decompensated cirrhosis.
- To evaluate the impact of DAAs on liver function, complications, and survival.
- To identify predictors of complications and survival post-DAA therapy.
Main Methods:
- A treatment group (n=160) received 3 months of DAAs for HCV decompensated cirrhosis.
- A matched control group (n=80) did not receive DAAs.
- Follow-up extended for 24-31 months, with assessments including liver volume via ultrasound.
Main Results:
- The DAA treatment group showed significant improvements in platelet count, albumin, Child-Turcotte-Pugh (CTP), and Model for End-Stage Liver Disease (MELD) scores.
- A notable reduction in hepatic encephalopathy (HE) frequency was observed, with 90% achieving sustained virologic response (SVR).
- Hepatocellular carcinoma (HCC) developed in 10% of treated patients; however, survival was significantly higher (28.9 months) compared to the control group (11.4 months). Liver volume < 495 ml predicted complications like HCC and reduced survival.
Conclusions:
- DAAs are effective in achieving high SVR rates (90%) in HCV patients with decompensated cirrhosis and adequate liver volume.
- DAA therapy improves CTP and MELD scores, reduces HE, and enhances survival.
- Adequate liver volume is crucial for favorable outcomes, and ultrasound measurement can predict complications and survival post-treatment.
Background:
Medical treatment of decompensated cirrhosis due to hepatitis C virus (HCV) remains a clinical challenge even in the era of direct-acting antiviral drugs (DAAs). We evaluated the efficacy and safety of DAAs in the management of HCV genotype 4-related decompensated cirrhosis.
Methods:
The study included a treatment group (n = 160) composed of HCV patients with decompensated cirrhosis who received DAAs for 3 months and a matched control group (n = 80) who preferred not to receive DAAs, follow-up was for 24-31 months.
Results:
In treatment group; there were improvements in platelet count, albumin, CTP (p = 0.001) and MELD scores (p = 0.03), a significant reduction in the frequency of hepatic encephalopathy (HE). SVR was achieved in 90%. Hepatocellular carcinoma (HCC) developed in 10% (n = 18) within 6.8 ± 2.5 months after DAAs, survival was higher in the treated vs. the control group (28.9 ± 0.95 vs. 11.4 ± 2.2 months, p = 0.001). Liver volume by ultrasound at a cutoff 495 ml was predictive of complications after DAAs therapy mainly HCC and reduced survival with sensitivity 93.2%, specificity 72%.
Conclusion:
HCV with decompensated cirrhosis and adequate liver volume had a 90% SVR with improved CTP&MELD and survival.
Clinical Trial:
(NCT03547895).
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