Development of hepatocellular carcinoma in patients with chronic hepatitis C who had sustained viral response following direct-acting antiviral therapy


Ebik B., Aygan M., TUNCEL E. T., Kacmaz H., Ekin N., ARPA M., ...Daha Fazla

Hepatology Forum, cilt.3, sa.3, ss.82-87, 2022 (Scopus, TRDizin)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 3 Sayı: 3
  • Basım Tarihi: 2022
  • Doi Numarası: 10.14744/hf.2022.2022.0016
  • Dergi Adı: Hepatology Forum
  • Derginin Tarandığı İndeksler: Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.82-87
  • Anahtar Kelimeler: Chronic Hepatitis C infection, direct-acting antiviral agents, hepatocellular carcinoma
  • Sağlık Bilimleri Üniversitesi Adresli: Evet

Özet

Background and Aim: Several studies have suggested that treatment with direct-acting antivirals (DAAs) in patients with chronic hepatitis C virus (HCV) may be associated with an increased risk of developing hepatocel-lular carcinoma (HCC). We investigated the incidence and risk factors of HCC in HCV patients who achieved a sustained virologic response (SVR) following DAA therapies. Materials and Methods: The medical data of patients who were diagnosed with HCV and received DAA therapy in two tertiary centers in Turkey were retrospectively collected. Results: Among them, 75 patients (52.4%) were noncirrhotic and 68 patients (47.6%) were cirrhotic. The overall SVR rate was 97.2% (139/143). It was 100% in noncirrhotic and 94.1% in cirrhotic patients. HCC was developed in 5 (7.4%) patients, all of whom had baseline cirrhosis. The annual rate of HCC occurrence was 2.94%, and the 5-year cumulative incidence of HCC was 7.3%. The mean Child-Pugh score (CPS) and Model for End-Stage Liver Disease (MELD) score significantly decreased after DAA treatment (CPS 7.0 vs 5.9, p=0.001; MELD 10.8 vs 9.5, p=0.003). Conclusion: There was no significant increase in the rate of HCC in cir-rhotic HCV patients treated with DAAs. This treatment led to a remark-ably high SVR rate and lowered CPS and MELD scores in cirrhotic HCV patients.