Follow-up Results of


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 13 05 2019
revised: 04 06 2019
accepted: 10 06 2019
entrez: 3 7 2019
pubmed: 3 7 2019
medline: 10 7 2019
Statut: ppublish

Résumé

We examined treatment the efficacy and data on long-term outcomes in real-world Japanese patients infected with hepatitis C virus (HCV) genotype 2 treated with 12-week sofosbuvir/ribavirin combination therapy. In a total of 86 patients who were treated with sofosbuvir/ribavirin, sustained virological response (SVR) rates and long-term-outcomes were retrospectively analyzed. The adherence to this combination therapy was 98.8%. The rates of SVR at week 24 (SVR24) achieved with this treatment according to the 'intention-to-treat' and 'per-protocol' analyses were 89.5% and 96.2%, respectively. Two patients who experienced relapse did not have any previously reported resistance-associated substitutions in the HCV non-structural protein 5B (NS5B) polymerase region. We did not observe any patients who experienced late relapse but did observe that 50% and 1.3% of patients with and without a previous history of hepatocellular carcinoma (HCC), respectively, developed HCC after achieving SVR24 (with a mean follow-up period of 2.7±0.8 years). Patients with SVR should be carefully followed-up to screen for the occurrence of HCC, although it is infrequent.

Sections du résumé

BACKGROUND BACKGROUND
We examined treatment the efficacy and data on long-term outcomes in real-world Japanese patients infected with hepatitis C virus (HCV) genotype 2 treated with 12-week sofosbuvir/ribavirin combination therapy.
PATIENTS AND METHODS METHODS
In a total of 86 patients who were treated with sofosbuvir/ribavirin, sustained virological response (SVR) rates and long-term-outcomes were retrospectively analyzed.
RESULTS RESULTS
The adherence to this combination therapy was 98.8%. The rates of SVR at week 24 (SVR24) achieved with this treatment according to the 'intention-to-treat' and 'per-protocol' analyses were 89.5% and 96.2%, respectively. Two patients who experienced relapse did not have any previously reported resistance-associated substitutions in the HCV non-structural protein 5B (NS5B) polymerase region. We did not observe any patients who experienced late relapse but did observe that 50% and 1.3% of patients with and without a previous history of hepatocellular carcinoma (HCC), respectively, developed HCC after achieving SVR24 (with a mean follow-up period of 2.7±0.8 years).
CONCLUSION CONCLUSIONS
Patients with SVR should be carefully followed-up to screen for the occurrence of HCC, although it is infrequent.

Identifiants

pubmed: 31262913
pii: 39/7/3855
doi: 10.21873/anticanres.13535
doi:

Substances chimiques

Antiviral Agents 0
RNA, Viral 0
Ribavirin 49717AWG6K
Sofosbuvir WJ6CA3ZU8B

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3855-3862

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Tomohiro Kaneko (T)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Tatsuo Kanda (T)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan kanda.tatsuo@nihon-u.ac.jp.

Kazushige Nirei (K)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Naoki Matsumoto (N)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Motomi Yamazaki (M)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Toshikatsu Shibata (T)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Akinori Tamura (A)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Masahiro Ogawa (M)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Noriko Nakajima (N)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Shunichi Matsuoka (S)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Kazumichi Kuroda (K)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Tomoe Komoriya (T)

Department of Sustainable Engineering, College of Industrial Technology, Nihon University, Chiba, Japan.

Tatsuo Yamamoto (T)

Department of Obstetrics and Gynecology, Nihon University School of Medicine, Tokyo, Japan.

Tadatoshi Takayama (T)

Department of Digestive Surgery, Nihon University School of Medicine, Tokyo, Japan.

Mitsuhiko Moriyama (M)

Division of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

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Classifications MeSH