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Aspirin Use and Risk of Breast Cancer in African American Women

Overview
Specialty Oncology
Date 2020 Sep 5
PMID 32887656
Citations 8
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Abstract

Background: Use of aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) has been hypothesized to be associated with reduced risk of breast cancer; however, results of epidemiological studies have been mixed. Few studies have investigated these associations among African American women.

Methods: To assess the relation of aspirin use to risk of breast cancer in African American women, we conducted a prospective analysis within the Black Women's Health Study, an ongoing nationwide cohort study of 59,000 African American women. On baseline and follow-up questionnaires, women reported regular use of aspirin (defined as use at least 3 days per week) and years of use. During follow-up from 1995 through 2017, 1919 invasive breast cancers occurred, including 1112 ER+, 569 ER-, and 284 triple-negative (TN) tumors. We used age-stratified Cox proportional hazards regression models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for associations of aspirin use with risk of ER+, ER-, and TN breast cancer, adjusted for established breast cancer risk factors.

Results: Overall, the HR for current regular use of aspirin relative to non-use was 0.92 (95% CI 0.81, 1.04). For ER+, ER-, and TN breast cancer, corresponding HRs were 0.98 (0.84, 1.15), 0.81 (0.64, 1.04), and 0.70 (0.49, 0.99), respectively.

Conclusions: Our findings with regard to ER- and TN breast cancer are consistent with hypothesized inflammatory mechanisms of ER- and TN breast cancer, rather than hormone-dependent pathways. Aspirin may represent a potential opportunity for chemoprevention of ER- and TN breast cancer.

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References
1.
Diaz-Cruz E, Brueggemeier R . Interrelationships between cyclooxygenases and aromatase: unraveling the relevance of cyclooxygenase inhibitors in breast cancer. Anticancer Agents Med Chem. 2006; 6(3):221-32. DOI: 10.2174/187152006776930873. View

2.
Glynn S, Prueitt R, Ridnour L, Boersma B, Dorsey T, Wink D . COX-2 activation is associated with Akt phosphorylation and poor survival in ER-negative, HER2-positive breast cancer. BMC Cancer. 2010; 10:626. PMC: 2993681. DOI: 10.1186/1471-2407-10-626. View

3.
Marshall S, Bernstein L, Anton-Culver H, Deapen D, Horn-Ross P, Mohrenweiser H . Nonsteroidal anti-inflammatory drug use and breast cancer risk by stage and hormone receptor status. J Natl Cancer Inst. 2005; 97(11):805-12. DOI: 10.1093/jnci/dji140. View

4.
Cairat M, Fournier A, Murphy N, Biessy C, Scalbert A, Rinaldi S . Nonsteroidal anti-inflammatory drug use and breast cancer risk in a European prospective cohort study. Int J Cancer. 2018; 143(7):1688-1695. PMC: 6837880. DOI: 10.1002/ijc.31570. View

5.
Basree M, Shinde N, Koivisto C, Cuitino M, Kladney R, Zhang J . Abrupt involution induces inflammation, estrogenic signaling, and hyperplasia linking lack of breastfeeding with increased risk of breast cancer. Breast Cancer Res. 2019; 21(1):80. PMC: 6637535. DOI: 10.1186/s13058-019-1163-7. View