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dc.contributor.author박영훈-
dc.date.accessioned2024-05-20T16:31:05Z-
dc.date.available2024-05-20T16:31:05Z-
dc.date.issued2024-
dc.identifier.issn2152-2650-
dc.identifier.otherOAK-34932-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/268416-
dc.description.abstractBackground: 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. © 2023-
dc.languageEnglish-
dc.publisherElsevier Inc.-
dc.subjectHepatitis B virus-
dc.subjectImmune suppression-
dc.subjectMultiple myeloma-
dc.subjectProphylaxis-
dc.subjectReactivation-
dc.titleOutcome of Multiple Myeloma Patients With Hepatitis B Surface Antigen: Korean Multiple Myeloma Working Party 2103 Study-
dc.typeArticle-
dc.relation.issue2-
dc.relation.volume24-
dc.relation.indexSCOPUS-
dc.relation.startpagee50-
dc.relation.lastpagee57.e2-
dc.relation.journaltitleClinical Lymphoma, Myeloma and Leukemia-
dc.identifier.doi10.1016/j.clml.2023.10.004-
dc.identifier.wosidWOS:001171228900001-
dc.identifier.scopusid2-s2.0-85176609469-
dc.author.googleYi-
dc.author.googleJun Ho-
dc.author.googleLee-
dc.author.googleJung Lim-
dc.author.googleYoo Jin-
dc.author.googleKang-
dc.author.googleHye Jin-
dc.author.googlePark-
dc.author.googleYoung Hoon-
dc.author.googleYuh-
dc.author.googleYoung Jin-
dc.author.googleLim-
dc.author.googleSung-Nam-
dc.author.googleKim-
dc.author.googleHyo Jung-
dc.author.googleJung-
dc.author.googleSung-Hoon-
dc.author.googleJe-Jung-
dc.author.googleCho-
dc.author.googleHee Jeong-
dc.author.googleMoon-
dc.author.googleJoon Ho-
dc.author.googleYhim-
dc.author.googleHo-Young-
dc.author.googleKihyun-
dc.contributor.scopusid박영훈(57212764446)-
dc.date.modifydate20240520120338-
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