体外受精与乳腺癌风险:综述。

M Salhab, W Al Sarakbi, Kefah Mokbel
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引用次数: 0

摘要

乳腺癌是一种典型的激素依赖性恶性肿瘤。作为体外受精(IVF)治疗的一部分,用于促排卵的药物会增加内源性性腺激素的水平,因此人们开始关注试管受精与患乳腺癌风险之间可能存在的关联。本文的目的是回顾文献并检查体外受精治疗对乳腺癌风险的潜在影响。方法:在英文文章中使用以下关键词进行Medline检索。利用相关文章的参考书目获得了更多的论文。此外,还对检索到的数据进行了综合分析。结果:确定了15项研究;其中11项为队列研究,4项为病例对照研究。没有一项单独的研究显示体外受精和乳腺癌之间有显著的整体联系,事实上,一项研究表明,在非怀孕期最大体重指数小于27.5的妇女中,用hCG治疗可以显著降低患乳腺癌的风险。对总共60,050名接受促排卵/体外受精治疗的妇女进行的队列研究的综合分析显示,这些治疗与乳腺癌风险增加之间没有显著关联(观察vs.预期:601 vs. 568,合并相对风险[RR] = 1.06, P = 0.337)。病例对照研究包括11303名乳腺癌组妇女和10930名对照组妇女。乳腺癌组接受体外受精的可能性略低(2.2% vs. 2.5%,总RR = 0.88, P = 0.231)。然而,一项研究表明,在有家族病史的女性中,不孕症治疗与边缘性乳腺癌风险增加有关。另一项研究表明,在使用生育药物的第一年内,乳腺癌的发病率比预期的要高,这可能是由于过量排卵引起的先前存在的癌症病变的促进,或者是由于在试管婴儿治疗过程中做出的早期诊断。关于生育治疗类型和乳腺癌风险的报道结果相互矛盾。结论:总的来说,没有明确的证据表明促排卵或体外受精会增加乳腺癌的风险。然而,由于早期诊断,第一年乳腺癌的发病率可能会有短暂的增加。此外,家族史呈阳性的女性患此病的风险可能会增加。未来的研究应该关注所使用的生育治疗类型和乳腺癌的风险。芳香化酶抑制剂作为标准促排卵药物的替代品应进一步评估。
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In vitro fertilization and breast cancer risk: a review.

Introduction: Breast cancer is a classic model of a hormone-dependent malignancy. Since the drugs used for ovulation induction as part of in vitro fertilization (IVF) treatment increase the levels of endogenous gonadal hormones, concerns have arisen regarding a possible association between IVF and the risk of developing breast cancer. The aim of this paper was to review the literature and examine the potential effects of IVF treatment on breast cancer risk.

Methods: Medline search was conducted using the key words below in English-language articles. Further papers were obtained using the bibliographies of relevant articles. Furthermore, a combined analysis of retrieved data was performed.

Results: Fifteen studies were identified; of these, 11 were cohort studies and 4 were case-control studies. None of the individual studies showed an overall significant association between IVF and breast cancer and, in fact, one study showed that treatment with hCG significantly reduced the risk of breast cancer in women whose maximum nonpregnant body mass index was less than 27.5. A combined analysis of the cohort studies including a total of 60,050 women treated with ovulation induction/IVF showed no significant association between these treatments and increased risk of breast cancer (observed vs. expected: 601 vs. 568, pooled relative risk [RR] = 1.06, P = 0.337). The case-control studies included a total of 11,303 women in the breast cancer groups and 10,930 controls. Women in the breast cancer groups were slightly less likely to have received IVF (2.2% vs. 2.5%, pooled RR = 0.88, P = 0.231). However, one study showed that infertility treatment was associated with an increased risk of breast cancer of borderline significance among women with a family history of the disease. Another study showed that the incidence of breast cancer within the first year of exposure to fertility drugs was higher than expected, possibly due to the promotion of preexisting cancer lesions caused by superovulation or due to the early diagnosis made in the course of IVF treatment. Conflicting results were reported regarding the type of fertility treatment and breast cancer risk.

Conclusion: Overall, there is no clear evidence that ovulation induction or IVF increases the risk of breast cancer. However, there may be a transient increase in the incidence of breast cancer in the first year due to earlier diagnosis. Furthermore, the risk may be increased in women with a positive family history. Future research should focus on the type of fertility treatment used and breast cancer risk. Aromatase inhibitors should be evaluated further as an alternative to standard ovulation-inducing drugs.

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