Prophylactic tenofovir alafenamide for hepatitis B virus reactivation and reactivation‐related hepatitis

Author:

Suda Goki1ORCID,Baba Masaru2,Yamamoto Yoshiya3,Sho Takuya1,Ogawa Koji1,Kimura Megumi1,Hosoda Shunichi1,Yoshida Sonoe1,Kubo Akinori1,Fu Qingjie1,Yang Zijian1,Tokuchi Yoshimasa1,Kitagataya Takashi1,Maehara Osamu4,Ohnishi Shunsuke4,Yamada Ren1,Ohara Masatsugu1,Kawagishi Naoki1,Natsuizaka Mitsuteru1,Nakai Masato1,Morikawa Kenichi1,Furuya Ken2,Suzuki Kazuharu13,Izumi Takaaki5,Meguro Takashi6,Terashita Katsumi7,Ito Jun8,Kobayashi Tomoe9,Tsunematsu Izumi10,Sakamoto Naoya1

Affiliation:

1. Departments of Gastroenterology and Hepatology, Graduate School of Medicine Hokkaido University Sapporo Japan

2. Department of Gastroenterology and Hepatology Japan Community Health Care Organization (JCHO) Hokkaido Hospital Hokkaido Japan

3. Department of Gastroenterology and Hepatology Hakodate City Hospital Hokkaido Japan

4. Laboratory of Molecular and Cellular Medicine, Faculty of Pharmaceutical Sciences Hokkaido University Sapporo Japan

5. Department of Gastroenterology and Hepatology Sapporo City General Hospital Hokkaido Japan

6. Department of Gastroenterology and Hepatology Hokkaido Gastroenterology Hospital Hokkaido Japan

7. Department of Gastroenterology and Hepatology Japan Community Health Care Organization (JCHO) Sapporo Hokushin Hospital Hokkaido Japan

8. Department of Gastroenterology and Hepatology The Hokkaido Medical Center Hokkaido Japan

9. Department of Gastroenterology and Hepatology Tomakomai City Hospital Hokkaido Japan

10. Touei Naika Clinic Hokkaido Japan

Abstract

AbstractNo prospective study on the efficacy of tenofovir alafenamide (TAF), a novel tenofovir prodrug, in preventing hepatitis B virus (HBV) reactivation has yet been reported. This multicenter prospective study enrolled HBV‐carriers who received TAF to prevent HBV reactivation before antitumor or immunosuppressive therapy, and patients with resolved HBV infection who experienced HBV‐reactivation and received TAF to prevent HBV reactivation‐related hepatitis. The efficacy of prophylactic TAF in preventing HBV reactivation and HBV reactivation‐related hepatitis was evaluated at 6 and 12 months after initiating TAF. Overall, 110 patients were administered TAF to prevent HBV reactivation or HBV reactivation‐related hepatitis. Three patients died owing to primary disease, whereas one patient was transferred to another hospital within 6 months after initiating TAF. Seven patients died due to primary disease, and five patients were transferred to another hospital within 12 months after initiating TAF. Therefore, 106 and 94 (77 patients with HBV infection, 17 with previous‐HBV infection) patients were evaluated at 6 and 12 months after initiating TAF, respectively. No patient experienced HBV reactivation, HBV reactivation‐related hepatitis, or treatment discontinuation due to HBV reactivation or adverse events of TAF after 6 and 12 months. TAF could effectively prevent HBV reactivation and HBV reactivation‐related hepatitis.

Funder

Japan Agency for Medical Research and Development

Gilead Sciences

Publisher

Wiley

Subject

Infectious Diseases,Virology

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