Phillips Kelly-Anne, Kotsopoulos Joanne, Domchek Susan M, Terry Mary Beth, Chamberlain James A, Bassett Julie K, Aeilts Amber M, Andrulis Irene L, Buys Saundra S, Cui Wanda, Daly Mary B, Eisen Andrea F, Foulkes William D, Friedlander Michael L, Gronwald Jacek, Hopper John L, John Esther M, Karlan Beth Y, Kim Raymond H, Kurian Allison W, Lubinski Jan, Metcalfe Kelly, Nathanson Katherine L, Singer Christian F, Southey Melissa C, Symecko Heather, Tung Nadine, Narod Steven A, Milne Roger L
Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC, Australia.
J Clin Oncol. 2025 Feb;43(4):422-431. doi: 10.1200/JCO.24.00176. Epub 2024 Oct 2.
It is uncertain whether, and to what extent, hormonal contraceptives increase breast cancer (BC) risk for germline or mutation carriers.
Using pooled observational data from four prospective cohort studies, associations between hormonal contraceptive use and BC risk for unaffected female and mutation carriers were assessed using Cox regression.
Of 3,882 and 1,509 mutation carriers, 53% and 71%, respectively, had ever used hormonal contraceptives for at least 1 year (median cumulative duration of use, 4.8 and 5.7 years, respectively). Overall, 488 and 191 mutation carriers developed BC during median follow-up of 5.9 and 5.6 years, respectively. Although for mutation carriers, neither current nor past use of hormonal contraceptives for at least 1 year was statistically significantly associated with BC risk (hazard ratio [HR], 1.40 [95% CI, 0.94 to 2.08], = .10 for current use; 1.16 [0.80 to 1.69], = .4, 1.40 [0.99 to 1.97], = .05, and 1.27 [0.98 to 1.63], = .07 for past use 1-5, 6-10, and >10 years before, respectively), ever use was associated with increased risk (HR, 1.29 [95% CI, 1.04 to 1.60], = .02). Furthermore, BC risk increased with longer cumulative duration of use, with an estimated proportional increase in risk of 3% (1%-5%, = .002) for each additional year of use. For mutation carriers, there was no evidence that current or ever use was associated with increased BC risk (HR, 0.70 [95% CI, 0.33 to 1.47], = .3 and 1.07 [0.73 to 1.57], = .7, respectively).
Hormonal contraceptives were associated with increased BC risk for mutation carriers, especially if used for longer durations. Decisions about their use in women with mutations should carefully weigh the risks and benefits for each individual.
激素避孕药是否以及在何种程度上会增加携带种系或突变的女性患乳腺癌(BC)的风险尚不确定。
利用四项前瞻性队列研究的汇总观察数据,采用Cox回归评估激素避孕药使用与未受影响女性及携带突变女性患BC风险之间的关联。
在3882名和1509名携带突变的女性中,分别有53%和71%的人曾使用激素避孕药至少1年(中位累积使用时间分别为4.8年和5.7年)。总体而言,在中位随访时间分别为5.9年和5.6年期间,分别有488名和191名携带突变的女性患BC。尽管对于携带突变的女性,目前或过去使用激素避孕药至少1年与BC风险在统计学上均无显著关联(风险比[HR],目前使用为1.40[95%置信区间,0.94至2.08],P = 0.10;过去使用1 - 5年为1.16[0.80至1.69],P = 0.4,过去使用6 - 10年为1.40[0.99至1.97],P = 0.05,过去使用超过10年为1.27[0.98至1.63],P = 0.07),但曾经使用与风险增加有关(HR,1.29[95%置信区间,1.04至1.60],P = 0.02)。此外,BC风险随累积使用时间延长而增加,估计每多使用一年风险比例增加3%(1% - 5%,P = 0.002)。对于携带突变的女性,没有证据表明目前或曾经使用与BC风险增加有关(HR,分别为0.70[95%置信区间,0.33至1.47],P = 0.3和1.07[0.73至1.57],P = 0.7)。
激素避孕药与携带突变的女性患BC风险增加有关,尤其是使用时间较长时。对于携带突变的女性,关于使用激素避孕药的决策应仔细权衡对每个个体的风险和益处。