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Effect of sofosbuvir and velpatasvir therapy on clinical outcome in hepatitis C virus patients with decompensated cirrhosis.
Tahata, Yuki; Sakamori, Ryotaro; Maesaka, Kazuki; Doi, Akira; Yamada, Ryoko; Kodama, Takahiro; Hikita, Hayato; Miyazaki, Masanori; Nozaki, Yasutoshi; Kaneko, Akira; Oshita, Masahide; Tanaka, Satoshi; Imanaka, Kazuho; Hiramatsu, Naoki; Morishita, Naoki; Ohkawa, Kazuyoshi; Yakushijin, Takayuki; Sakakibara, Mitsuru; Iio, Sadaharu; Doi, Yoshinori; Tatsumi, Tomohide; Takehara, Tetsuo.
Affiliation
  • Tahata Y; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Sakamori R; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Maesaka K; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Doi A; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Yamada R; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Kodama T; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Hikita H; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Miyazaki M; Osaka Police Hospital, Osaka, Japan.
  • Nozaki Y; Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.
  • Kaneko A; Japan Community Healthcare Organization Osaka Hospital, Osaka, Japan.
  • Oshita M; Ikeda Municipal Hospital, Ikeda, Osaka, Japan.
  • Tanaka S; National Hospital Organization Osaka National Hospital, Osaka, Japan.
  • Imanaka K; Itami City Hospital, Itami, Hyogo, Japan.
  • Hiramatsu N; Osaka Rosai Hospital, Sakai, Osaka, Japan.
  • Morishita N; Minoh City Hospital, Minoh, Osaka, Japan.
  • Ohkawa K; Osaka International Cancer Institute, Osaka, Japan.
  • Yakushijin T; Osaka General Medical Center, Osaka, Japan.
  • Sakakibara M; Yao Municipal Hospital, Yao, Osaka, Japan.
  • Iio S; Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Hyogo, Japan.
  • Doi Y; Otemae Hospital, Osaka, Japan.
  • Tatsumi T; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
  • Takehara T; Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Hepatol Res ; 53(4): 301-311, 2023 Apr.
Article in En | MEDLINE | ID: mdl-36507871
ABSTRACT

AIM:

To determine the impact of direct-acting antiviral therapy on the long-term prognosis of decompensated cirrhotic patients.

METHODS:

A total of 37 patients with hepatitis C virus-induced decompensated cirrhosis treated with sofosbuvir and velpatasvir (SOF/VEL group) were prospectively enrolled. For historical control, 65 hepatitis C virus-positive decompensated cirrhotic patients who did not receive direct-acting antiviral therapy were included (control group). The incidence rates of hepatocellular carcinoma (HCC), decompensated events with hospitalization, and overall survival were compared between both groups.

RESULTS:

A total of 41 patients experienced decompensated events during 15.0 months in the control group, and six patients during 21.6 months in the SOF/VEL group. The cumulative incidence rates of decompensated events after 2 years were significantly higher in the control group (53.1%) than in the SOF/VEL group (14.5%; p < 0.001). A total of 27 patients died within 22.0 months in the control group, and three patients died within 25.6 months in the SOF/VEL group. The overall survival rates after 2 years were significantly lower in the control group (67.6%) than in the SOF/VEL group (91.3%; p = 0.010). A total of 13 patients in the control group developed HCC during 15.8 months, and 10 patients during 17.3 months in the SOF/VEL group. The HCC incidence rates after 2 years were 20.3% and 29.6% in the control and SOF/VEL groups, respectively, with no significant difference (p = 0.327).

CONCLUSIONS:

SOF/VEL therapy may suppress the development of decompensated events and improve the prognosis in decompensated cirrhotic patients; however, the incidence of HCC remains prevalent in these patients irrespective of SOF/VEL therapy.
Key words

Full text: 1 Database: MEDLINE Type of study: Prognostic_studies Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Type of study: Prognostic_studies Language: En Year: 2023 Type: Article