Hepatitis B virus reactivation in seronegative occult hepatitis B patient receiving ibrutinib therapy.


Journal

Virology journal
ISSN: 1743-422X
Titre abrégé: Virol J
Pays: England
ID NLM: 101231645

Informations de publication

Date de publication:
01 08 2023
Historique:
received: 08 06 2023
accepted: 25 07 2023
medline: 3 8 2023
pubmed: 2 8 2023
entrez: 1 8 2023
Statut: epublish

Résumé

Ibrutinib is a Bruton's tyrosine kinase (BTK) inhibitor approved for the treatment for several mature B-cell malignancies. Reactivation of hepatitis B virus (HBV) is a well-described complication in patients with chronic HBV infection or prior HBV exposure undergoing cytotoxic or immunosuppressive chemotherapy for hematologic malignancies. This phenomenon has been frequently reported with rituximab. However, published data on the risk of HBV reactivation induced by ibrutinib are scarce. Cases of HBV reactivation in hematologic patients receiving ibrutinib therapy have recently been described, but limited only to overt hepatitis B patients or seropositive occult hepatitis B patients. We report the first case of HBV reactivation during ibrutinib treatment in an asymptomatic 82-year-old woman with seronegative occult hepatitis B patient (i.e., negative for HBsAg, anti-HBc and anti-HBs). Four months after ibrutinib treatment, her liver function test (LFT) was deranged, with seroconversion to HBsAg positivity. Serum hepatitis B virus DNA was quantified to be 1.92 × 10 Our case illustrated that in populations with a high incidence of HBV exposure, systematic screening for HBV exposure is essential prior to ibrutinib treatment, followed by serial monitoring of serologic and molecular markers of hepatitis B. There is a need for an international consensus to support the recommendation of antiviral prophylaxis against HBV reactivation in patients using ibrutinib.

Sections du résumé

BACKGROUND
Ibrutinib is a Bruton's tyrosine kinase (BTK) inhibitor approved for the treatment for several mature B-cell malignancies. Reactivation of hepatitis B virus (HBV) is a well-described complication in patients with chronic HBV infection or prior HBV exposure undergoing cytotoxic or immunosuppressive chemotherapy for hematologic malignancies. This phenomenon has been frequently reported with rituximab. However, published data on the risk of HBV reactivation induced by ibrutinib are scarce. Cases of HBV reactivation in hematologic patients receiving ibrutinib therapy have recently been described, but limited only to overt hepatitis B patients or seropositive occult hepatitis B patients.
CASE PRESENTATION
We report the first case of HBV reactivation during ibrutinib treatment in an asymptomatic 82-year-old woman with seronegative occult hepatitis B patient (i.e., negative for HBsAg, anti-HBc and anti-HBs). Four months after ibrutinib treatment, her liver function test (LFT) was deranged, with seroconversion to HBsAg positivity. Serum hepatitis B virus DNA was quantified to be 1.92 × 10
CONCLUSIONS
Our case illustrated that in populations with a high incidence of HBV exposure, systematic screening for HBV exposure is essential prior to ibrutinib treatment, followed by serial monitoring of serologic and molecular markers of hepatitis B. There is a need for an international consensus to support the recommendation of antiviral prophylaxis against HBV reactivation in patients using ibrutinib.

Identifiants

pubmed: 37528444
doi: 10.1186/s12985-023-02140-w
pii: 10.1186/s12985-023-02140-w
pmc: PMC10394758
doi:

Substances chimiques

ibrutinib 1X70OSD4VX
Hepatitis B Surface Antigens 0
Hepatitis B Antibodies 0
Antiviral Agents 0
DNA, Viral 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

168

Informations de copyright

© 2023. The Author(s).

Références

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Auteurs

Lok-Ka Lam (LK)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hongkong.

Thomas Sau Yan Chan (TSY)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hongkong.

Yu-Yan Hwang (YY)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hongkong.

Lung-Yi Mak (LY)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hongkong.
State Key Laboratory of Liver Research, The University of Hong Kong, Pokfulam, Hongkong.

Wai-Kay Seto (WK)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hongkong.
State Key Laboratory of Liver Research, The University of Hong Kong, Pokfulam, Hongkong.

Yok-Lam Kwong (YL)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hongkong.

Man-Fung Yuen (MF)

Department of Medicine, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hongkong. mfyuen@hkucc.hku.hk.
State Key Laboratory of Liver Research, The University of Hong Kong, Pokfulam, Hongkong. mfyuen@hkucc.hku.hk.
Queen Mary Hospital, Professorial Block, 102, Pokfulam Road, Hong Kong. mfyuen@hkucc.hku.hk.

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Classifications MeSH