Successful treatment by glecaprevir/pibrentasvir followed by hepatoprotective therapy of acute chronic hepatitis exacerbation caused by daratumumab-based regimen for multiple myeloma: Case report and review of the literature

J Infect Chemother. 2021 Dec;27(12):1750-1755. doi: 10.1016/j.jiac.2021.07.018. Epub 2021 Jul 31.

Abstract

Hepatitis C virus (HCV) exacerbation is relatively rare as compared with hepatitis B virus reactivation in patients treated with immunosuppressive or anticancer drugs. We herein present the first reported case of acute exacerbation of chronic hepatitis in a patient with HCV persistent infection caused by combination treatment with daratumumab (DARA), bortezomib, and dexamethasone (DVd therapy). A 79-year-old woman diagnosed as having chronic HCV infection 11 years prior without successful viral elimination was referred to our hospital for the treatment of acute liver injury. Multiple myeloma (MM; IgG-κ type) was diagnosed two years before referral and subjected to several treatments. She had commenced DVd therapy four months prior to admission. Since her liver enzymes did not normalize with drug discontinuation and hepatoprotective therapy, we suspected HCV exacerbation and began direct-acting antiviral (DAA) treatment with glecaprevir/pibrentasvir (GLE/PIB). Soon afterwards, her liver enzymes normalized, and she achieved a sustained virological response after 8 weeks of treatment. Clinicians should bear in mind HCV exacerbation when encountering chronic HCV with acute liver injury under MM treatment including a DARA-based regimen. In such cases, DAA therapy is an option when other urgent treatments are needed.

Keywords: Daratumumab; Exacerbation; Glecaprevir/pibrentasvir; Hepatitis C virus.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aged
  • Aminoisobutyric Acids
  • Antibodies, Monoclonal
  • Antiviral Agents
  • Benzimidazoles
  • Cyclopropanes
  • Female
  • Genotype
  • Hepacivirus / genetics
  • Hepatitis C, Chronic* / drug therapy
  • Humans
  • Lactams, Macrocyclic
  • Leucine / analogs & derivatives
  • Multiple Myeloma*
  • Proline / analogs & derivatives
  • Pyrrolidines
  • Quinoxalines
  • Sulfonamides

Substances

  • Aminoisobutyric Acids
  • Antibodies, Monoclonal
  • Antiviral Agents
  • Benzimidazoles
  • Cyclopropanes
  • Lactams, Macrocyclic
  • Pyrrolidines
  • Quinoxalines
  • Sulfonamides
  • pibrentasvir
  • daratumumab
  • Proline
  • Leucine
  • glecaprevir