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Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection
BACKGROUND: Reports of hepatitis B virus (HBV) reactivation in solid tumors are very limited, and their frequencies and risk factors were previously unknown. AIM: To evaluate the prevalence and risk factors of HBV reactivation in patients with solid tumors with resolved HBV infection. METHODS: All 1...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379615/ https://www.ncbi.nlm.nih.gov/pubmed/29984542 http://dx.doi.org/10.1111/ajco.13050 |
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author | Kotake, Takeshi Satake, Hironaga Okita, Yoshihiro Hatachi, Yukimasa Hamada, Mamiko Omiya, Masatomo Yasui, Hisateru Hashida, Toru Kaihara, Satoshi Inokuma, Tetsuro Tsuji, Akihito |
author_facet | Kotake, Takeshi Satake, Hironaga Okita, Yoshihiro Hatachi, Yukimasa Hamada, Mamiko Omiya, Masatomo Yasui, Hisateru Hashida, Toru Kaihara, Satoshi Inokuma, Tetsuro Tsuji, Akihito |
author_sort | Kotake, Takeshi |
collection | PubMed |
description | BACKGROUND: Reports of hepatitis B virus (HBV) reactivation in solid tumors are very limited, and their frequencies and risk factors were previously unknown. AIM: To evaluate the prevalence and risk factors of HBV reactivation in patients with solid tumors with resolved HBV infection. METHODS: All 1088 patients with solid tumors were assessed for eligibility; 251 patients had resolved HBV infection (negative for HBs antigen and positive for anti‐HBc antibody and/or positive for anti‐HBs antibody), and HBV‐DNA was assessed for 243 of these patients in whom we analyzed the prevalence of HBV reactivation. Risk factors for HBV reactivation were exploratorily evaluated by analysis of a case–control study. RESULTS: The prevalence of HBV‐DNA reactivation was 2.1% (95% confidence interval [CI], 0.3–3.9%). We did not observe any exacerbation of HBV‐DNA by early intervention. A low anti‐HBs antibody titer (<10.0 mIU/mL) and high average daily dexamethasone dose (>1.0 mg/day) were high risk factors, with odds ratios of 5.94 (95% CI, 1.15–30.6, P = 0.03) and 8.69 (95% CI, 1.27–58.8, P = 0.02), respectively. CONCLUSION: HBV reactivation in solid tumor patients was relatively rare. Therefore, risk factors that can identify targets for HBV screening must be determined in future studies. |
format | Online Article Text |
id | pubmed-7379615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73796152020-07-24 Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection Kotake, Takeshi Satake, Hironaga Okita, Yoshihiro Hatachi, Yukimasa Hamada, Mamiko Omiya, Masatomo Yasui, Hisateru Hashida, Toru Kaihara, Satoshi Inokuma, Tetsuro Tsuji, Akihito Asia Pac J Clin Oncol Original Articles BACKGROUND: Reports of hepatitis B virus (HBV) reactivation in solid tumors are very limited, and their frequencies and risk factors were previously unknown. AIM: To evaluate the prevalence and risk factors of HBV reactivation in patients with solid tumors with resolved HBV infection. METHODS: All 1088 patients with solid tumors were assessed for eligibility; 251 patients had resolved HBV infection (negative for HBs antigen and positive for anti‐HBc antibody and/or positive for anti‐HBs antibody), and HBV‐DNA was assessed for 243 of these patients in whom we analyzed the prevalence of HBV reactivation. Risk factors for HBV reactivation were exploratorily evaluated by analysis of a case–control study. RESULTS: The prevalence of HBV‐DNA reactivation was 2.1% (95% confidence interval [CI], 0.3–3.9%). We did not observe any exacerbation of HBV‐DNA by early intervention. A low anti‐HBs antibody titer (<10.0 mIU/mL) and high average daily dexamethasone dose (>1.0 mg/day) were high risk factors, with odds ratios of 5.94 (95% CI, 1.15–30.6, P = 0.03) and 8.69 (95% CI, 1.27–58.8, P = 0.02), respectively. CONCLUSION: HBV reactivation in solid tumor patients was relatively rare. Therefore, risk factors that can identify targets for HBV screening must be determined in future studies. John Wiley and Sons Inc. 2018-07-08 2019-02 /pmc/articles/PMC7379615/ /pubmed/29984542 http://dx.doi.org/10.1111/ajco.13050 Text en © 2018 The Authors. Asia‐Pacific Journal of Clinical Oncology Published by John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Kotake, Takeshi Satake, Hironaga Okita, Yoshihiro Hatachi, Yukimasa Hamada, Mamiko Omiya, Masatomo Yasui, Hisateru Hashida, Toru Kaihara, Satoshi Inokuma, Tetsuro Tsuji, Akihito Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection |
title | Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection |
title_full | Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection |
title_fullStr | Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection |
title_full_unstemmed | Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection |
title_short | Prevalence and risk factors of hepatitis B virus reactivation in patients with solid tumors with resolved HBV infection |
title_sort | prevalence and risk factors of hepatitis b virus reactivation in patients with solid tumors with resolved hbv infection |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379615/ https://www.ncbi.nlm.nih.gov/pubmed/29984542 http://dx.doi.org/10.1111/ajco.13050 |
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