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Time-course changes in liver functional reserve after successful sofosbuvir/velpatasvir treatment in patients with decompensated cirrhosis.
Atsukawa, Masanori; Tsubota, Akihito; Kondo, Chisa; Toyoda, Hidenori; Nakamuta, Makoto; Takaguchi, Koichi; Watanabe, Tsunamasa; Hiraoka, Atsushi; Uojima, Haruki; Ishikawa, Toru; Iwasa, Motoh; Tada, Toshifumi; Nozaki, Akito; Chuma, Makoto; Fukunishi, Shinya; Asano, Toru; Ogawa, Chikara; Abe, Hiroshi; Kato, Keizo; Hotta, Naoki; Shima, Toshihide; Matsuura, Kentaro; Mikami, Shigeru; Tachi, Yoshihiko; Fujioka, Shinichi; Okubo, Hironao; Shimada, Noritomo; Tani, Joji; Morishita, Asahiro; Hidaka, Isao; Moriya, Akio; Tsuji, Kunihiko; Akahane, Takehiro; Okubo, Tomomi; Arai, Taeang; Kitamura, Michika; Morita, Kiyoshi; Kawata, Kazuhito; Tanaka, Yasuhito; Kumada, Takashi; Iwakiri, Katsuhiko.
Affiliation
  • Atsukawa M; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Tsubota A; Core Research Facilities for Basic Science, The Jikei University School of Medicine, Tokyo, Japan.
  • Kondo C; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Toyoda H; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
  • Nakamuta M; Department of Gastroenterology, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
  • Takaguchi K; Department of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Kagawa, Japan.
  • Watanabe T; Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
  • Hiraoka A; Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Ehime, Japan.
  • Uojima H; Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Kanagawa, Japan.
  • Ishikawa T; Department of Hepatology, Saiseikai Niigata Hospital, Niigata, Japan.
  • Iwasa M; Department of Gastroenterology and Hepatology, Mie University School of Medicine, Mie, Japan.
  • Tada T; Department of Gastroenterology, Himeji Red Cross Hospital, Hyogo, Japan.
  • Nozaki A; Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Chuma M; Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Fukunishi S; Second Department of Internal Medicine, Osaka Medical College, Osaka, Japan.
  • Asano T; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Tokyo Metropolitan Bokutoh Hospital, Tokyo, Japan.
  • Ogawa C; Department of Gastroenterology and Hepatology, Takamatsu Red Cross Hospital, Takamatsu, Japan.
  • Abe H; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Shinmatusdo Central General Hospital, Matsudo, Japan.
  • Kato K; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Shinmatusdo Central General Hospital, Matsudo, Japan.
  • Hotta N; Department of Internal Medicine, Division of Hepatology, Masuko Memorial Hospital, Nagoya, Japan.
  • Shima T; Department of Gastroenterology and Hepatology, Saiseikai Suita Hospital, Suita, Japan.
  • Matsuura K; Department of Virology & Liver Unit, Nagoya City University, Graduate School of Medical Sciences, Aichi, Japan.
  • Mikami S; Department of Internal Medicine, Division of Gastroenterology, Kikkoman General Hospital, Noda, Japan.
  • Tachi Y; Bantane Hospital, Fujita Health University School of Medicine, Nagoya, Japan.
  • Fujioka S; Department of Gastroenterology, Okayama Saiseikai General Hospital, Okayama, Japan.
  • Okubo H; Department of Gastroenterology, Juntendo Nerima University Hospital, Tokyo, Japan.
  • Shimada N; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Otakanomori Hospital, Kashiwa, Japan.
  • Tani J; Department of Gastroenterology, Kagawa University Graduate School of Medicine, Kagawa, Japan.
  • Morishita A; Department of Gastroenterology, Kagawa University Graduate School of Medicine, Kagawa, Japan.
  • Hidaka I; Department of Gastroenterology and Hepatology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
  • Moriya A; Department of Gastroenterology, Mitoyo General Hospital, Kannonji, Japan.
  • Tsuji K; Gastroenterology Center, Teine Keijinkai Hospital, Sapporo, Japan.
  • Akahane T; Department of Gastroenterology, Japanese Red Cross Ishinomaki Hospital, Ishinomaki, Japan.
  • Okubo T; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Arai T; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Kitamura M; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Morita K; Gastroenterology, Toyota Kosei Hospital, Toyota, Japan.
  • Kawata K; Hepatology Division, Department of Internal Medicine II, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Tanaka Y; Department of Virology & Liver Unit, Nagoya City University, Graduate School of Medical Sciences, Aichi, Japan.
  • Kumada T; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
  • Iwakiri K; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
Hepatol Res ; 52(3): 235-246, 2022 Mar.
Article in En | MEDLINE | ID: mdl-34861090
ABSTRACT

AIM:

Direct-acting antivirals (DAAs) are currently available even for patients with decompensated cirrhosis. Reportedly, hepatic functional reserve improved in the short term after achievement of sustained virologic response (SVR). We aimed to clarify the outcomes after achievement of SVR in patients with decompensated cirrhosis who were treated by DAAs in real-world clinical practice.

METHODS:

A prospective, multicenter study of 12-week sofosbuvir/velpatasvir was conducted in 86 patients with decompensated cirrhosis, who were evaluated for 48 weeks post-treatment.

RESULTS:

The cohort included 8 patients with Child-Pugh class A, 56 with B, and 22 with C. The proportion of Child-Pugh class A patients increased from 9.1% at baseline to 44.1% at 48 weeks post-treatment, while that of class B and C patients decreased from 66.2% to 35.1% and from 24.7% to 14.3%, respectively. Among the patients with Child-Pugh class B and C, univariate analysis identified low total bilirubin, Child-Pugh score, Child-Pugh class B, ALBI score, and high serum albumin as factors associated with improvement to Child-Pugh class A. The optimal cut-off value of the factors for predicting improvement to Child-Pugh class A were 1.4 mg/dl for total bilirubin, 2.9 g/dl for serum albumin, 8 points for Child-Pugh score, and -1.88 for ALBI score.

CONCLUSION:

Achievement of SVR with sofosbuvir/velpatasvir improved the liver functional reserve at 12 weeks post-treatment and maintained the stable effects until 48 weeks post-treatment in patients with decompensated cirrhosis. Specifically, the patients with less advanced conditions had the likelihood of improving to Child-Pugh class A at 48 weeks post-treatment.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Hepatol Res Year: 2022 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Hepatol Res Year: 2022 Document type: Article Affiliation country: Japón
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