Biostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
J Natl Cancer Inst. 2012 Jul 3;104(13):1021-7. doi: 10.1093/jnci/djs255. Epub 2012 Jul 6.
Fertility drugs stimulate hyperovulation, which may have implications for breast cancer. We examined the association between use of fertility drugs (clomiphene citrate [CC] and follicle-stimulating hormone [FSH]) and subsequent risk of young-onset (<50 years at diagnosis) breast cancer.
We conducted the Two Sister Study, a sister-matched case-control study, by enrolling 1422 women between September 2008 and December 2010, who were younger than age 50 years at diagnosis with breast cancer and were enrolled within 4 years of diagnosis, and 1669 breast cancer-free control sisters from the Sister Study. Participants reported their use of fertility drugs (CC and FSH) and ever-users reported whether a pregnancy had resulted that lasted 10 or more (10+) weeks. Conditional logistic regression was used to estimate confounder-adjusted odds ratios (ORs) and 95% confidence intervals (CIs) for fertility drug use with or without conception of a 10+ week pregnancy.
A total of 288 participants reported having used ovulation-stimulating drugs (193 CC only, 29 FSH only, and 66 both). Overall, women who had used fertility drugs showed a non-statistically significantly decreased risk of breast cancer, compared with nonusers (OR = 0.82, 95% CI = 0.63 to 1.08). Women who had used fertility drugs but had not conceived a 10+ week pregnancy under treatment showed a statistically significantly decreased risk of breast cancer compared with nonusers (OR = 0.62, 95% CI = 0.43 to 0.89). Women who had used fertility drugs and conceived a 10+ week pregnancy under treatment showed a statistically significantly increased risk of breast cancer compared with unsuccessfully treated women (OR = 1.82, 95% CI = 1.10 to 3.00), although their risk was not increased compared with women who had not used fertility drugs (OR = 1.13, 95% CI = 0.78 to 1.64).
In the absence of a 10+ week pregnancy under treatment, exposure to ovulation-stimulating fertility drugs was associated with reduced risk of young-onset breast cancer. This apparent association was absent in women who conceived a 10+ week pregnancy under treatment, for whom risk was higher than that of unsuccessfully treated women, but similar to that of untreated women.
生育药物刺激超排卵,这可能对乳腺癌有影响。我们研究了生育药物(克罗米芬[CC]和卵泡刺激素[FSH])的使用与年轻发病(<50 岁)乳腺癌风险之间的关系。
我们通过招募 1422 名年龄在 50 岁以下、发病后 4 年内确诊为乳腺癌的患者,以及来自姐妹研究的 1669 名乳腺癌无病对照姐妹,开展了一项姐妹匹配病例对照研究——双妹研究。参与者报告了他们使用生育药物(CC 和 FSH)的情况,曾使用者报告是否有妊娠持续 10 周或以上(10+ 周)。采用条件逻辑回归来估计生育药物使用与妊娠 10+ 周之间的混杂因素调整比值比(OR)和 95%置信区间(CI)。
共有 288 名参与者报告使用过促排卵药物(193 名仅使用 CC,29 名仅使用 FSH,66 名同时使用)。总体而言,与未使用者相比,使用生育药物的女性患乳腺癌的风险呈非统计学显著降低(OR=0.82,95%CI=0.63 至 1.08)。在治疗期间使用生育药物但未受孕 10 周以上的女性与未使用者相比,患乳腺癌的风险呈统计学显著降低(OR=0.62,95%CI=0.43 至 0.89)。在治疗期间使用生育药物并受孕 10 周以上的女性与未成功治疗的女性相比,患乳腺癌的风险呈统计学显著升高(OR=1.82,95%CI=1.10 至 3.00),但与未使用生育药物的女性相比,风险并未升高(OR=1.13,95%CI=0.78 至 1.64)。
在未治疗情况下受孕 10 周以上的情况下,接触促排卵生育药物与降低年轻发病乳腺癌风险相关。在治疗期间受孕 10 周以上的女性中,这种明显的相关性不存在,她们的风险高于未成功治疗的女性,但与未治疗的女性相似。