4.8 Article

Use of systemic glucocorticoids and risk of breast cancer in a prospective cohort of postmenopausal women

Journal

BMC MEDICINE
Volume 19, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12916-021-02004-6

Keywords

Glucocorticoids; Breast cancer; Molecular status; Cancer stage; Oestrogen receptors; Postmenopausal women; Cohort; Pharmacoepidemiology

Funding

  1. French National Research Agency (ANR) under the Investment for the Future Program (PIA) [ANR-10-COHO-0006]
  2. French Ministry of Higher Education, Research and Innovation [2102 918823]
  3. French National Cancer Institute [INCa_13539]
  4. French League Against Cancer (LNCC)

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This study suggests that the association between systemic glucocorticoid use and breast cancer risk may differ by tumor subtype and stage.
BackgroundGlucocorticoids could theoretically decrease breast cancer risk through their anti-inflammatory effects or increase risk through immunosuppression. However, epidemiological evidence is limited regarding the associations between glucocorticoid use and breast cancer risk.MethodsWe investigated the association between systemic glucocorticoid use and breast cancer incidence in the E3N cohort, which includes 98,995 women with information on various characteristics collected from repeated questionnaires complemented with drug reimbursement data available from 2004. Women with at least two reimbursements of systemic glucocorticoids in any previous 3-month period since January 1, 2004, were defined as exposed. We considered exposure as a time-varying parameter, and we used multivariable Cox regression models to estimate hazard ratios (HRs) of breast cancer. We performed a competing risk analysis using a cause-specific hazard approach to study the heterogeneity by tumour subtype/stage/grade.ResultsAmong 62,512 postmenopausal women (median age at inclusion of 63 years old), 2864 developed breast cancer during a median follow-up of 9 years (between years 2004 and 2014). Compared with non-exposure, glucocorticoid exposure was not associated with overall breast cancer risk [HR = 0.94 (0.85-1.05)]; however, it was associated with a higher risk of in situ breast cancer and a lower risk of invasive breast cancer [HRinsitu = 1.34 (1.01-1.78); HRinvasive = 0.86 (0.76-0.97); P-homogeneity = 0.01]. Regarding the risk of invasive breast cancer, glucocorticoid exposure was inversely associated with oestrogen receptor (ER)-positive breast cancer [HRER+ = 0.82 (0.72-0.94); HRER- = 1.21 (0.88-1.66); P-homogeneity = 0.03]; it was also inversely associated with the risk of stage 1 or stage 2 tumours but positively associated with the risk of stage 3/4 breast cancers [HRstage1 = 0.87 (0.75-1.01); HRstage2 = 0.67 (0.52-0.86); HRstage3/4 = 1.49 (1.02-2.20); P-homogeneity = 0.01].ConclusionThis study suggests that the association between systemic glucocorticoid use and breast cancer risk may differ by tumour subtype and stage.

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