Risk of estrogen receptor-specific breast cancer by family history of estrogen receptor subtypes and other cancers

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Abstract

Background: The extent to which the risk of estrogen receptor (ER)-specific breast cancer is associated with ER status of breast cancer and other cancers among first-degree relatives is unclear. Methods: This population-based cohort included 464 707 cancer-free women in Stockholm, Sweden, during 1978-2019. For ERnegative and ER-positive breast cancers, we estimated hazard ratios (HRs) associated with ER status of female first-degree relatives with breast cancer and of other cancers in all first-degree relatives. Associations between ER-negative and ER-positive status by family cancer history were estimated using logistic regression in a case-only design. Results: Women with familial ER-positive breast cancer had 1.87 times (95% confidence interval [CI] = 1.77 to 1.97) higher risk of ER-positive subtype, whereas the corresponding hazard ratio for ER-negative was 2.54 (95% CI = 2.08 to 3.10) when having familial ER-negative breast cancer. The risk increased with an increasing number of female first-degree relatives having concordant subtypes and younger age at diagnosis (Ptrend

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APA

Wang, Q. L., Zhang, Y., Zeng, E., Grassmann, F., He, W., & Czene, K. (2023). Risk of estrogen receptor-specific breast cancer by family history of estrogen receptor subtypes and other cancers. Journal of the National Cancer Institute, 115(9), 1020–1028. https://doi.org/10.1093/jnci/djad104

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