Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Mar;9(3):1506-1517.
doi: 10.21037/tcr.2020.01.63.

Hepatitis B virus infection specially increases risk of liver metastasis in breast cancer patients: a propensity-matched analysis

Affiliations

Hepatitis B virus infection specially increases risk of liver metastasis in breast cancer patients: a propensity-matched analysis

Ping Yu et al. Transl Cancer Res. 2020 Mar.

Abstract

Background: Breast cancer and hepatitis B virus (HBV) infection are serious public health issues in China. But the effect of HBV infection on breast cancer remains unclear. The objective was to assess whether HBV infection was associated with prognosis of breast cancer.

Methods: A retrospective database of 1,924 invasive breast cancer patients from Sun Yat-sen University Cancer Center from 2008 to 2010 was established. Propensity score matching method was applied to balance baseline parameters. Logistic regression was used for identifying the independent risk factors of liver metastasis. Prognostic outcomes were evaluated via Kaplan-Meier analysis and Cox model.

Results: Primary evaluation of gross data suggested HBV infection was associated with much higher rate of liver metastasis. 642 patients were matched for analysis. The median follow-up time was about 69 months. Patients with HBV surface antigen (HBsAg) (+) had a specially higher risk of liver metastasis aside of other distant organs than those with HBsAg (-). HBsAg (-/+) was identified to be an independent risk factor of liver metastasis [odds ratio (OR), 2.651; 95% confidence intervals (CI), 1.213-5.796; P=0.015]. HBsAg (+) was associated with liver metastasis significantly in stage III or in estrogen receptor (ER) (+) and/or progesterone receptor (PR) (+), human epidermal growth factor receptor-2 (HER-2) (-) subtype. Meanwhile, patients with HBsAg (+) had significant shorter liver metastasis-free survival (LMFS) compared with HBsAg (-) patients (P=0.041). But the difference of overall survival (OS) between the HBsAg (-) and HBsAg (+) groups reached statistically no significance (P=0.425). The multivariate analysis suggested HBsAg (+) could worsen the outcome of LMFS [hazards ratio (HR), 2.450; 95% CI, 1.169-5.135; P=0.018].

Conclusions: In breast cancer, HBsAg (+) was associated with specially a higher rate of liver metastasis and thus worsened the LMFS. HBsAg (-/+) was an independent risk factor of liver metastasis.

Keywords: Hepatitis B virus (HBV); breast cancer; liver metastasis; survival.

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr.2020.01.63). The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Flow chart of the patient selection.
Figure 2
Figure 2
Kaplan-Meier OS (A), LMFS (B) curves for the 642 patients with HBsAg (−/+). OS, overall survival; LMFS, liver metastasis-free survival; HBsAg, hepatitis B surface antigen.

Similar articles

Cited by

References

    1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin 2019;69:7-34. 10.3322/caac.21551 - DOI - PubMed
    1. DeSantis CE, Ma J, Gaudet MM, et al. Breast cancer statistics, 2019. CA Cancer J Clin 2019;69:438-51. 10.3322/caac.21583 - DOI - PubMed
    1. Schwartz RS, Erban JK. Timing of Metastasis in Breast Cancer. N Engl J Med 2017;376:2486-8. 10.1056/NEJMcibr1701388 - DOI - PubMed
    1. Schweitzer A, Horn J, Mikolajczyk RT, et al. Estimations of worldwide prevalence of chronic hepatitis B virus infection: a systematic review of data published between 1965 and 2013. Lancet 2015;386:1546-55. 10.1016/S0140-6736(15)61412-X - DOI - PubMed
    1. Ott JJ, Horn J, Krause G, et al. Time trends of chronic HBV infection over prior decades - A global analysis. J Hepatol 2017;66:48-54. 10.1016/j.jhep.2016.08.013 - DOI - PubMed