Sex hormones and the risk of keratinocyte cancers among women in the United States: A population‐based case–control study
LF Kuklinski, MS Zens, AE Perry… - … journal of cancer, 2016 - Wiley Online Library
International journal of cancer, 2016•Wiley Online Library
Men are at a higher risk of developing both squamous cell carcinoma (SCC) and basal cell
carcinoma (BCC) than women, but there is emerging evidence that women may be
experiencing greater increases in the incidence rates of these malignancies than men. One
possible explanation is the expanding use of sex steroids among women, although only a
few studies have examined this hypothesis. As part of a population‐based, case–control
study of women in New Hampshire, USA, we sought to evaluate the risk of SCC, BCC, and …
carcinoma (BCC) than women, but there is emerging evidence that women may be
experiencing greater increases in the incidence rates of these malignancies than men. One
possible explanation is the expanding use of sex steroids among women, although only a
few studies have examined this hypothesis. As part of a population‐based, case–control
study of women in New Hampshire, USA, we sought to evaluate the risk of SCC, BCC, and …
Men are at a higher risk of developing both squamous cell carcinoma (SCC) and basal cell carcinoma (BCC) than women, but there is emerging evidence that women may be experiencing greater increases in the incidence rates of these malignancies than men. One possible explanation is the expanding use of sex steroids among women, although only a few studies have examined this hypothesis. As part of a population‐based, case–control study of women in New Hampshire, USA, we sought to evaluate the risk of SCC, BCC, and early‐onset BCC in relation to exogenous and endogenous sex hormones. We found that oral contraceptive (OC) use was associated with an increased risk of SCC (OR = 1.4, 95% CI = 1.1–1.8) and BCC (OR = 1.4, 95% CI = 1.0‐1.8), particularly high estrogen dose (>50 mg) OC use. Hormone replacement therapy (HRT) use also related to SCC, with an elevated OR largely for progestin use (OR = 1.4, 95% CI = 1.1–1.8). Additionally, both OC use and combination HRT use were associated with more aggressive BCC subtypes. In contrast, menstrual and reproductive history did not appear to influence keratinocyte cancer risk in our data. Our findings provide evidence that use of sex steroids may enhance risk of keratinocyte cancer.
