Reproductive Endocrinology, RAMBAM Health Care Campus, The Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa.
Pinchas Borenstein Talpiot Medical Leadership Program, Department of Obstetrics and Gynecology, Chaim Sheba Medical Center, Tel Hashomer, Sackler School of Medicine, Tel Aviv University, Israel.
Ann Oncol. 2014 Sep;25(9):1719-1728. doi: 10.1093/annonc/mdu036. Epub 2014 Mar 20.
The late effects of cancer treatment have recently gained a worldwide interest among reproductive endocrinologists, oncologists, and all health-care providers, and the protection against iatrogenic infertility caused by chemotherapy assumes a high priority. Here, we summarize the case for and against using GnRH-agonist for fertility preservation and minimizing chemotherapy-induced gonadotoxicity. The rationale and philosophy supporting its use is that preventing premature ovarian failure (POF) is preferable to treating it, following the dictum: 'an ounce of prevention is worth a pound of cure'. Despite many publications on this subject, there are many equivocal issues necessitating summary. Until now, 20 studies (15 retrospective and 5 randomized, controlled trials) have reported on 1837 patients treated with GnRH-a in parallel to chemotherapy, showing a significant decrease in POF rate in survivors versus 9 studies reporting on 593 patients, with results not supporting GnRH-a use. Patients treated with GnRH-a in parallel to chemotherapy preserved their cyclic ovarian function in 91% of cases when compared with 41% of controls, with a pregnancy rate of 19-71% in the treated patients. Furthermore, seven meta-analyses have concluded that GnRH-a are beneficial and may decrease the risk of POF in survivors. However, controversy still remains regarding the efficiency of GnRH-a in preserving fertility. Since not all the methods involving fertility preservation are unequivocally successful and safe, these young patients deserve to be informed of all the various modalities to minimize gonadal damage and preserve ovarian function and future fertility. Combining several methods for a specific patient may increase the odds for minimally invasive fertility preservation.
癌症治疗的晚期效应最近引起了生殖内分泌学家、肿瘤学家和所有医疗保健提供者的全球关注,防止化疗引起的医源性不孕具有很高的优先级。在这里,我们总结了使用 GnRH 激动剂进行生育力保存和最大限度减少化疗引起的性腺毒性的利弊。支持其使用的理由和理念是,预防卵巢早衰 (POF) 优于治疗 POF,遵循这一原则:“预防胜于治疗”。尽管有许多关于这个主题的出版物,但仍有许多有争议的问题需要总结。到目前为止,已有 20 项研究(15 项回顾性和 5 项随机对照试验)报道了 1837 例接受 GnRH-a 与化疗同时治疗的患者,与 9 项报道 593 例患者的研究相比,幸存者的 POF 发生率显著降低,但结果不支持 GnRH-a 的使用。与对照组相比,接受 GnRH-a 与化疗同时治疗的患者在 91%的情况下保持了卵巢周期性功能,治疗患者的妊娠率为 19-71%。此外,7 项荟萃分析得出结论,GnRH-a 是有益的,可以降低幸存者 POF 的风险。然而,关于 GnRH-a 在保留生育能力方面的有效性仍存在争议。由于并非所有涉及生育力保存的方法都明确有效且安全,因此这些年轻患者应该了解各种方法,以最大限度地减少性腺损伤并保持卵巢功能和未来的生育能力。为特定患者结合几种方法可能会增加微创生育力保存的机会。