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Outcome of Multiple Myeloma Patients With Hepatitis B Surface Antigen: Korean Multiple Myeloma Working Party 2103 Study

  • Jun Ho Yi
  • , Jung Lim Lee
  • , Yoo Jin Lee
  • , Hye Jin Kang
  • , Young Hoon Park
  • , Young Jin Yuh
  • , Sung Nam Lim
  • , Hyo Jung Kim
  • , Sung Hoon Jung
  • , Je Jung Lee
  • , Hee Jeong Cho
  • , Joon Ho Moon
  • , Ho Young Yhim
  • , Kihyun Kim*
  • *Corresponding author for this work
  • Chung-Ang University
  • Daegu Fatima Hospital
  • University of Ulsan
  • Korea Institute of Radiological and Medical Sciences
  • Ewha Womans University
  • Inje University
  • Hallym University
  • Chonnam National University
  • Kyungpook National University
  • Samsung Medical Center, Sungkyunkwan university

Research output: Contribution to journalJournal articlepeer-review

Abstract

Background: Hepatitis B virus reactivation (HBVr) is a well-known complication of systemic chemotherapy for particularly hematologic malignancies in HBV carriers. We performed a multicenter retrospective study to investigate the incidence and risk factors of HBVr in patients with hepatitis B surface antigen (HBsAg)-positive multiple myeloma (MM). Methods: We included 123 patients with HBsAg-positive MM who had received systemic therapy. The primary objective of the study was to evaluate the incidence of HBVr in patients with HBsAg-positive MM. Results: The median age was 59 years, and 72 patients were male. With a median follow-up duration of 41.4 months, there were 43 instances of HBVr in 35 patients (28.5%): 29 treatment-related HBVr occurred during 424 treatments. Treatments containing antiviral prophylaxis were associated with a significantly lower incidence of HBVr compared to those without (14.4% vs. 1.9%, P < 0.001). Moreover, treatment with cyclophosphamide (P = 0.002) and doxorubicin (P = 0.053) were risk factors for HBVr; stem cell transplantation was not associated with HBVr. There was no significant difference in overall survival between patients with and without HBVr (P = 0.753) and myeloma progression was the major cause of death. Conclusion: Considering the low incidence of HBVr in patients who had received antiviral prophylaxis, HBsAg-positivity should not impede patients from receiving optimal antimyeloma treatment or participating in clinical trials.

Original languageEnglish
Pages (from-to)e50-e57.e2
JournalClinical Lymphoma, Myeloma and Leukemia
Volume24
Issue number2
DOIs
StatePublished - 2024.02

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Hepatitis B virus
  • Immune suppression
  • Multiple myeloma
  • Prophylaxis
  • Reactivation

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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