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A Prospective Study of Preemptive Tenofovir Disoproxil Fumarate Therapy in HBsAg-Positive Patients With Diffuse Large B-Cell Lymphoma Receiving Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone

Authors
 Do Young Kim  ;  Yu Ri Kim  ;  Cheolwon Suh  ;  Dok Hyun Yoon  ;  Deok-Hwan Yang  ;  Yong Park  ;  Hyeon Seok Eom  ;  Jeong-Ok Lee  ;  Jae-Yong Kwak  ;  Hye Jin Kang  ;  Shin Young Hyun  ;  Jae-Cheol Jo  ;  Myung Hee Chang  ;  Kwai Han Yoo  ;  Sung-Nam Lim  ;  Ho-Jin Shin  ;  Won Seog Kim  ;  In-Ho Kim  ;  Min Kyung Kim  ;  Hyo Jung Kim  ;  Won-Sik Lee  ;  Yeung-Chul Mun  ;  Jin Seok Kim 
Citation
 AMERICAN JOURNAL OF GASTROENTEROLOGY, Vol.118(8) : 1373-1380, 2023-08 
Journal Title
AMERICAN JOURNAL OF GASTROENTEROLOGY
ISSN
 0002-9270 
Issue Date
2023-08
MeSH
Alanine Transaminase ; Antiviral Agents / therapeutic use ; Cyclophosphamide / therapeutic use ; DNA, Viral ; Doxorubicin / therapeutic use ; Hepatitis B Surface Antigens ; Hepatitis B virus ; Hepatitis B, Chronic* ; Humans ; Lymphoma, Large B-Cell, Diffuse* / chemically induced ; Lymphoma, Large B-Cell, Diffuse* / drug therapy ; Prednisone / therapeutic use ; Prospective Studies ; Rituximab / adverse effects ; Tenofovir / adverse effects ; Vincristine / adverse effects
Abstract
Introduction: This prospective study aimed to investigate the efficacy and safety of preemptive antiviral therapy with tenofovir disoproxil fumarate (TDF) for HBsAg-positive patients with newly diagnosed diffuse large B-cell lymphoma receiving rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) chemotherapy.

Methods: We enrolled 73 patients from 20 institutions. The primary end point was the absolute risk of hepatitis B virus (HBV)-related hepatitis during preemptive TDF therapy and for 24 weeks after withdrawal from TDF. Hepatitis was defined as a more than 3-fold increase in serum alanine aminotransferase from baseline or an alanine aminotransferase level of ≥100 U/L. HBV-related hepatitis was defined as hepatitis with an increase in serum HBV-DNA to >10 times that of the pre-exacerbation baseline or an absolute increase of ≥20,000 IU/mL compared with the baseline.

Results: No patient developed HBV reactivation or HBV-related hepatitis during preemptive antiviral therapy (until 48 weeks after completion of R-CHOP chemotherapy) with TDF. All adverse events were grade 1 or 2. HBV reactivation was reported in 17 (23.3%) patients. All HBV reactivation was developed at a median of 90 days after withdrawal from TDF (range, 37-214 days). Six (8.2%) patients developed HBV-related hepatitis at a median of 88 days after withdrawal from TDF (range, 37-183 days).

Discussion: Preemptive TDF therapy in HBsAg-positive patients with diffuse large B-cell lymphoma receiving R-CHOP chemotherapy was safe and effective for preventing HBV-related hepatitis. However, a long-term maintenance strategy of preemptive TDF therapy should be recommended because of the relatively high rate of HBV-related hepatitis after withdrawal from TDF ( ClinicalTrials.gov ID: NCT02354846).

Copyright © 2023 by The American College of Gastroenterology.
Full Text
https://journals.lww.com/ajg/fulltext/2023/08000/a_prospective_study_of_preemptive_tenofovir.18.aspx
DOI
10.14309/ajg.0000000000002185
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Do Young(김도영)
Kim, Yu Ri(김유리) ORCID logo https://orcid.org/0000-0001-5505-0142
Kim, Jin Seok(김진석) ORCID logo https://orcid.org/0000-0001-8986-8436
Hyun, Shin Yong(현신영) ORCID logo https://orcid.org/0000-0002-8137-8675
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/196263
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