Elevation of the Hepatitis B Virus DNA during the Treatment of Polycythemia Vera with the JAK Kinase Inhibitor Ruxolitinib

Intern Med. 2016;55(10):1341-4. doi: 10.2169/internalmedicine.55.5529. Epub 2016 May 15.

Abstract

Ruxolitinib is a useful treatment option for myelofibrosis since it effectively resolves splenomegaly and constitutional symptoms. After the widespread use of ruxolitinib outside of clinical trials, a series of case reports indicated a potential risk of ruxolitinib-associated opportunistic infections, including the reactivation of the hepatitis B virus (HBV). We herein report the case of a polycythemia vera patient who showed an elevation of HBV-DNA viral DNA with an elevation of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) after the initiation of ruxolitinib. Anti-viral therapy with entecavir was immediately started and the HBV viral load thereafter decreased with an improvement of the liver function. Physicians should thus be aware of the potential risk of ruxolitinib-associated HBV reactivation.

MeSH terms

  • Alanine Transaminase / blood
  • Aspartate Aminotransferases / blood
  • DNA, Viral / biosynthesis*
  • Female
  • Guanine / analogs & derivatives
  • Guanine / therapeutic use
  • Hepatitis B virus / metabolism*
  • Humans
  • Janus Kinases / antagonists & inhibitors*
  • Middle Aged
  • Nitriles
  • Polycythemia Vera / drug therapy*
  • Pyrazoles / adverse effects*
  • Pyrazoles / therapeutic use
  • Pyrimidines
  • Splenomegaly

Substances

  • DNA, Viral
  • Nitriles
  • Pyrazoles
  • Pyrimidines
  • entecavir
  • Guanine
  • ruxolitinib
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Janus Kinases