Low incidence of hepatitis B virus reactivation in patients with hematological malignancies receiving novel anticancer drugs: A report from a high epidemic area and literature review

被引:2
|
作者
Yan, Zheng [1 ]
Luo, Xu-Feng [2 ,3 ]
Yao, Shu-Na [1 ]
Wang, Hai-Ying [1 ]
Chu, Jun-Feng [1 ]
Zhao, Shuang [1 ]
Song, Ming [2 ]
Wei, Xu-Dong [4 ]
Zhou, Ke-Shu [4 ]
Li, Yu-Fu [3 ]
Zhou, Wen-Ping [1 ,2 ]
Zhang, Jiu-Yang [1 ,3 ]
Zhang, Pei-Pei [5 ]
Zhou, Li -Li [5 ]
Wang, Xian-Wei [6 ]
Yao, Zhi-Hua [1 ,7 ]
Liu, Yan-Yan [1 ,7 ]
机构
[1] Zhengzhou Univ, Dept Internal Med, Affiliated Canc Hosp, Zhengzhou, Peoples R China
[2] Zhengzhou Univ, Dept Clin Res Management, Affiliated Canc Hosp, Zhengzhou, Peoples R China
[3] Zhengzhou Univ, Inst Lymphoma Res, Affiliated Canc Hosp, Zhengzhou, Peoples R China
[4] Zhengzhou Univ, Hematol Dept, Affiliated Canc Hosp, Zhengzhou, Peoples R China
[5] Zhengzhou Univ, Lab Dept, Affiliated Canc Hosp, Zhengzhou, Peoples R China
[6] Zhengzhou Univ, Cent Lab, Affiliated Canc Hosp, Zhengzhou, Peoples R China
[7] Shengzhou Univ, Dept Internal Med, Affiliated Canc Hosp, 127 Dongming Rd, Zhengzhou 450008, Henan, Peoples R China
关键词
Hematological malignancy; HBV reactivation; Lymphoma; Novel anticancer drug; Incidence; HBV REACTIVATION; DARATUMUMAB; INFECTION; IBRUTINIB; LYMPHOMA;
D O I
10.1016/j.jmii.2023.04.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: More and more novel anticancer drugs have been approved for patients with hematological malignancies in recent years, but HBV reactivation (HBV-R) data in this population is very scarce. This study aimed to evaluated HBV-R risk in patients with hematological malignancies receiving novel anticancer drugs.Methods: HBV markers and serum HBV DNA levels of patients with hematological malignancies receiving novel anticancer drugs in a tertiary cancer hospital were retrospectively collected. HBV-R risk in the whole cohort and subgroups was described. The relevant literature was re-viewed to make a pooled analysis.Results: Of 845 patients receiving novel anticancer drugs, 258 (30.5%) were considered at risk for HBV-R. The median duration of exposure to novel drugs was 5.6 (0.1-67.6) months. The incidence of HBV-R was 2.1% in patients with past HBV infection without prophylactic antiviral treatment (PAT) and 1.2% in all patients at risk of HBV-R. In a pooled analysis of 11 studies with 464 patients, the incidence of HBV-R was 2.4% (95% CI: 1.3-4.2) in all at-risk patients receiving novel anticancer drugs and 0.6% (95% CI: 0.03-3.5) in patients with anticancer drugs plus PAT. The incidence of death due to HBV-R was 0.4% (95% CI: 0.1-1.6) in all at-risk patients and 18.2% (95% CI: 3.2-47.7) in patients with HBV-R.Conclusion: Most episodes of HBV-R are preventable, and most cases with HBV-R are manage-able. We recommend that novel anticancer drugs should not be intentionally avoided when treating cancer patients with HBV infection. Copyright <feminine ordinal indicator> 2023, Taiwan Society of Microbiology. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:747 / 756
页数:10
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