Fatum Muhammad, McVeigh Enda, Child Tim
Oxford Fertility Unit, Institute of Reproductive Sciences, Nuffield Department of Obstetrics and Gynaecology, University of Oxford , Oxford , UK.
Hum Fertil (Camb). 2013 Dec;16(4):235-40. doi: 10.3109/14647273.2013.800650. Epub 2013 Jul 17.
Breast cancer is one of the hormone-dependent cancers that may be adversely affected by elevated oestrogen or progesterone concentrations, particularly the endocrine active (hormone receptor positive) breast cancers. Treatment for breast cancer patients aimed at fertility preservation, includes ovarian hyperstimulation, the harvest of oocytes, and subsequent cryopreservation of oocytes or embryos. Classically, gonadotrophins have been used effectively for ovulation induction, a treatment often accompanied by high blood oestrogen concentrations produced by the hyperstimulated granulosa cells. Despite the uncertainty which surrounds this issue and the lack of clear-cut clinical evidence, it is still of major concern that these ensuing high hormone levels might be associated with a high risk of recurrence of the cancer. A growing number of clinical studies have strongly suggested the benefits of using aromatase inhibitors in infertility treatment, both as single agents or as adjuncts to FSH-containing ovulation induction regimes in reproductive medicine. Combining gonadotrophins with aromatase inhibitors would augment the stimulation effect, with a reduced increase in serum concentrations of estradiol. We propose to open a debate over the use of aromatase inhibitors in combination with FSH in ovulation induction treatment of breast cancer oncofertility patients. As the safety of aromatase inhibitors such as letrozole has recently been demonstrated in several studies, and there is growing concern over the possible detrimental effects of high estradiol levels on breast cancer cells (at least in mouse models), the co-administration of letrozole in these patients would reduce both the high supraphysiologic serum levels of estradiol and the intratumoral in situ production of oestrogen. However, since it is unlikely that a well-founded evidence-based justification of this treatment will be formulated in the near future, based on well-designed prospective randomised controlled trials, we advocate a wider use of aromatase inhibitors in combination with gonadotrophins in breast cancer patients, especially those with hormone-receptor-positive tumours.
乳腺癌是激素依赖性癌症之一,可能会受到雌激素或孕激素浓度升高的不利影响,尤其是内分泌活性(激素受体阳性)乳腺癌。针对乳腺癌患者的生育力保存治疗包括卵巢过度刺激、卵母细胞采集以及随后的卵母细胞或胚胎冷冻保存。传统上,促性腺激素已被有效地用于诱导排卵,这种治疗通常伴随着过度刺激的颗粒细胞产生的高血雌激素浓度。尽管围绕这个问题存在不确定性且缺乏明确的临床证据,但人们仍然主要担心这些随之而来的高激素水平可能与癌症复发的高风险相关。越来越多的临床研究强烈表明,在不孕症治疗中使用芳香化酶抑制剂有益,无论是作为单一药物还是作为生殖医学中含促卵泡素的诱导排卵方案的辅助药物。将促性腺激素与芳香化酶抑制剂联合使用会增强刺激效果,同时降低雌二醇血清浓度的升高。我们提议就芳香化酶抑制剂与促卵泡素联合用于乳腺癌肿瘤生育力患者的诱导排卵治疗展开讨论。由于来曲唑等芳香化酶抑制剂的安全性最近在多项研究中得到了证实,并且人们越来越担心高雌二醇水平对乳腺癌细胞可能产生的有害影响(至少在小鼠模型中),在这些患者中联合使用来曲唑将降低高生理水平以上的血清雌二醇水平以及肿瘤内雌激素的原位产生。然而,由于基于精心设计的前瞻性随机对照试验,近期不太可能形成关于这种治疗的充分循证依据,我们主张在乳腺癌患者,尤其是激素受体阳性肿瘤患者中更广泛地使用芳香化酶抑制剂与促性腺激素联合治疗。