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FRI0273 Reactivation of Hepatitis B Virus in Patients Treated with Anti-TNF Therapy
  1. S.M. Jung1,
  2. J.Y. Kang1,
  3. H.K. Min1,
  4. J.H. Koh1,
  5. Y.S. Suh1,
  6. J.H. Lee1,
  7. J. Lee1,
  8. J.Y. Lee1,
  9. J.-M. Kim2,
  10. S.-K. Kwok1,
  11. J.H. Ju1,
  12. K.-S. Park1,
  13. H.-Y. Kim3,
  14. S.-H. Park1
  1. 1Internal Medicine, The Catholic University Of Korea, Seoul
  2. 2Internal Medicine, Keimyung University School of Medicine, Dongsan Medical Center, Daegu
  3. 3Internal Medicine, Konkuk University Hospital, School of Medicine, Seoul, Korea, Republic Of

Abstract

Background Anti-TNF therapy was known to increase the risk of certain infection. There are no sufficient data about the reactivation of hepatitis B virus (HBV) after anti-TNF therapy.

Objectives The study was aimed to investigate the clinical course of hepatitis B in patients with rheumatoid arthritis (RA) and ankylosing spondylitis (AS) after the introduction of anti-TNF therapy.

Methods We retrospectively reviewed to identify patients infected with HBV treated with TNF inhibitors between October, 2004 and September, 2013. For patients with HBV infection, the liver enzyme and the viral status were monitored. The HBV reactivation was defined according to the Korean guideline by hepatology.

Results Of 983 patients (RA, n=536; AS, n=447) who were treated with TNF inhibitors, 23 patients (RA, n=17; AS, n=6) had comorbidities of HBV infection. Eighteen patients were treated with etanercept, three with adalimumab, and two with infliximab. Seven patients received pre-emptive antiviral prophylaxis before anti-TNF therapy: 4 with entecavir, 1 with telbivudine, 1 with tenofovir, and 1 with lamivudine. Among 23 patients with HBV infection, 4 (17.4%) patients experienced the reactivation of HBV, which occurred in 3 patients without prophylaxis and 1 patient with lamivudine prophylaxis. In the latter case, YMDD mutation was identified and addition of adefovir resulted in virological response. The other three patients were treated successfully with entecavir or tenofovir. There was no subsequent events associated with HBV infection.

Conclusions This study indicates the risk of HBV reactivation after anti-TNF therapy. Careful management is mandatory for patients who planned to be treated with TNF inhibitors.

References

  1. Vassilopoulos D, Calabrese LH. Management of rheumatic disease with comorbid HBV or HCV infection. Nature reviews Rheumatology. 2012 Jun;8(6):348-57

  2. Oketani M, Ido A, Uto H, Tsubouchi H. Prevention of hepatitis B virus reactivation in patients receiving immunosuppressive therapy or chemotherapy. Hepatology research: the official journal of the Japan Society of Hepatology. 2012 Jul;42(7):627-36

  3. Korean Association for the Study of the L. KASL Clinical Practice Guidelines: Management of chronic hepatitis B. Clinical and molecular hepatology. 2012 Jun;18(2):109-62

Acknowledgements This study was supported by a grant from the Korea Healthcare Technology R&D Project, Ministry of Health and Welfare, Republic of Korea (HI10C2020).

Disclosure of Interest None declared

DOI 10.1136/annrheumdis-2014-eular.5251

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