Long-acting, progestin-based contraceptives and risk of breast, gynecological, and other cancers

Karen M Tuesley, Katrina Spilsbury, Sallie-Anne Pearson, Peter Donovan, Andreas Obermair, Michael D Coory, Sitwat Ali, Nirmala Pandeya, Louise Stewart, Susan J Jordan, Penelope M Webb
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Abstract

Background Use of long-acting, reversible contraceptives has increased over the past 20 years, but an understanding of how they could influence cancer risk is limited. Methods We conducted a nested case-control study among a national cohort of Australian women (n = 176 601 diagnosed with cancer between 2004 and 2013; 882 999 matched control individuals) to investigate the associations between the levonorgestrel intrauterine system, etonogestrel implants, depot-medroxyprogesterone acetate and cancer risk and compared these results with the oral contraceptive pill. We used conditional logistic regression to estimate odds ratios (OR) and 95% confidence intervals (CI). Results Levonorgestrel intrauterine system and etonogestrel implant use was associated with breast cancer risk (OR = 1.26, 95% CI = 1.21 to 1.31, and OR = 1.24, 95% CI = 1.17 to 1.32, respectively), but depot-medroxyprogesterone acetate was not, except when used for 5 or more years (OR = 1.23, 95% CI = 0.95 to 1.59). Reduced risks were seen for levonorgestrel intrauterine system (≥1 years of use) in endometrial cancer (OR = 0.80, 95% CI = 0.65 to 0.99), ovarian cancer (OR = 0.71, 95% CI = 0.57 to 0.88), and cervical cancer (OR = 0.62, 95% CI = 0.51 to 0.75); for etonogestrel implant in endometrial cancer (OR = 0.21, 95% CI = 0.13 to 0.34) and ovarian cancer (OR = 0.76, 95% CI = 0.57 to 1.02); and for depot-medroxyprogesterone acetate in endometrial cancer (OR = 0.21, 95% CI = 0.13 to 0.34). Although levonorgestrel intrauterine system, etonogestrel implant and depot-medroxyprogesterone acetate were all associated with increased cancer risk overall, for etonogestrel implant, the risk returned to baseline after cessation, similar to the oral contraceptive pill. We were unable to adjust for all potential confounders, but sensitivity analyses suggested that adjusting for parity, smoking, and obesity would not have materially changed our findings. Conclusion Long-acting, reversible contraceptives have similar cancer associations to the oral contraceptive pill (reduced endometrial and ovarian cancer risks and short-term increased breast cancer risk). This information may be helpful to women and their physicians when discussing contraception options.
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基于孕激素的长效避孕药与乳腺癌、妇科癌症和其他癌症的风险
背景 过去20年来,长效、可逆避孕药的使用有所增加,但人们对它们如何影响癌症风险的了解却很有限。方法 我们对澳大利亚全国妇女队列(n = 176 601,2004-2013年间确诊为癌症;882 999名匹配对照个体)进行了一项巢式病例对照研究,以调查左炔诺孕酮宫内避孕系统、依托诺孕酮植入剂、醋酸去甲羟孕酮与癌症风险之间的关系,并将这些结果与口服避孕药进行比较。我们使用条件逻辑回归法估算了几率比(OR)和 95% 的置信区间(CI)。结果 使用左炔诺孕酮宫内避孕系统和伊托诺孕酮植入剂与乳腺癌风险有关(OR = 1.26,95% CI = 1.21 至 1.31;OR = 1.24,95% CI = 1.17 至 1.32),但醋酸去甲羟孕酮与乳腺癌风险无关,使用 5 年或 5 年以上者除外(OR = 1.23,95% CI = 0.95 至 1.59)。左炔诺孕酮宫内避孕系统(使用≥1 年)在子宫内膜癌(OR = 0.80,95% CI = 0.65 至 0.99)、卵巢癌(OR = 0.71,95% CI = 0.57 至 0.88)和宫颈癌(OR = 0.62,95% CI = 0.51 至 0.75)方面的风险降低;依托孕酮宫内避孕系统(使用≥1 年)在子宫内膜癌(OR = 0.80,95% CI = 0.65 至 0.99)、卵巢癌(OR = 0.71,95% CI = 0.57 至 0.88)和宫颈癌(OR = 0.62,95% CI = 0.51 至 0.75)方面的风险降低。75);子宫内膜癌(OR = 0.21,95% CI = 0.13 至 0.34)和卵巢癌(OR = 0.76,95% CI = 0.57 至 1.02)中的依托孕烯植入物;子宫内膜癌(OR = 0.21,95% CI = 0.13 至 0.34)中的醋酸去甲羟孕酮(OR = 0.21,95% CI = 0.13 至 0.34)。虽然左炔诺孕酮宫内避孕系统、依托诺孕酮植入剂和醋酸去甲羟孕酮总体上都与癌症风险增加有关,但就依托诺孕酮植入剂而言,停药后风险恢复到基线,与口服避孕药类似。我们无法对所有潜在的混杂因素进行调整,但敏感性分析表明,对奇偶性、吸烟和肥胖进行调整不会对我们的研究结果产生实质性的改变。结论 长效、可逆避孕药与口服避孕药的癌症相关性相似(子宫内膜癌和卵巢癌风险降低,乳腺癌风险短期内增加)。这些信息可能会对妇女及其医生讨论避孕选择时有所帮助。
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