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临床试验/NCT03954197
NCT03954197Unknown不适用

Evaluation of Priming Before in Vitro Maturation for Fertility Preservation in Breast Cancer Patients: a Randomized Controlled Study

Hôpital Jean Verdier2 个研究点 分布在 1 个国家目标入组 204 人开始时间: 2014年9月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
204
试验地点
2
主要终点
total number of mature oocytes cryopreserved

研究概览

简要总结

Oocyte vitrification after in vitro maturation (IVM) is one of the main techniques for preserving female fertility before chemotherapy for breast cancer. In this technique, originally developed for patients with ovarian pathology, polycystic ovarian syndrome, induction of an LH peak has been shown to improve outcomes. Young women with breast cancer, who are candidates for urgent fertility preservation, do not have ovarian pathology. The objective of the present study is to assess whether the absence of therapeutic intervention prior to oocyte retrieval for IVM in these patients is at least as effective as the injection of hCG or GnRH agonist used in routine practice.

详细描述

In vitro maturation (IVM) is an assisted reproductive technology which consists in the retrieval of immature cumulus-oocyte complexes (COCs) from small antral follicles, followed by their in vitro maturation in specific culture conditions. Oocytes having reached metaphase II (MII) stage after 24 to 48 hours of IVM can then be fertilized. This procedure was first developed for patients presenting polycystic ovarian syndrome (PCOS), in order to avoid ovarian hyperstimulation syndrome (OHSS), an iatrogenic consequence of exogenous gonadotropins administration. However, the increasing use of GnRH antagonist protocols allowing ovulation trigger with GnRH agonist has dramatically reduced the indication of IVM in women at risk of OHSS. Yet, evidence indicate that IVM may be considered for patients presenting FSH resistance or contraindications to controlled ovarian stimulation. The recent development of female fertility preservation (FP) renewed interest to this technique. Indeed, it can be performed without any prior ovarian stimulation and whatever the phase of the menstrual cycle. Although it is still considered experimental, oocyte vitrification following IVM has been applied in different groups of patients, in particular those diagnosed with breast cancer, autoimmune or ovarian diseases. In physiologic conditions, final follicular maturation is induced by a double FSH and LH release which occurs when the dominant follicle reaches approximately 17 to 20 mm in diameter. This gonadotropin surge usually precedes the follicular rupture and mature oocyte release from 36 to 40 hours. In case of an assisted reproductive treatment, two strategies can be used to reproduce this hormonal signal: (i) either an injection of hCG, which binds to the LH receptor on granulosa cells, (ii) or a GnRH agonist (GnRHa) administration which induces an endogenous double peak of LH and FSH through a "flare up effect". Miming common practice for in vitro fertilization, priming with hCG or GnRHa injection 36 hours before the COCs retrieval has been suggested for patients undergoing IVM procedure in order to improve oocyte maturation rates and further IVM outcomes. Indeed, it is hypothesized that these iatrogenic hormonal activities might enhance the final oocyte maturation in vivo, therefore shortening the duration of the overall IVM process. Actually, in PCOS patients, several line of evidence indicate that IVM outcomes are improved after hCG priming. This positive effect might be explained by a premature expression of LH receptors on granulosa cells of small antral follicles <10 mm in diameter. Nevertheless, in normo-ovulatory non PCOS patients, LH receptor expression in these follicles remains very low, questioning the relevance of providing LH activity to improve oocyte maturation during IVM cycles performed for FP. The present investigation aimed to test whether the absence of therapeutic intervention prior to oocyte retrieval modifies IVM outcomes when compared with cycles primed either with recombinant hCG or GnRH agonist in breast cancer patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 38 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • age between 18 and 38 years;
  • diagnosis of breast cancer (BC)
  • indication for neoadjuvant chemotherapy;
  • body mass index (BMI) ≤27kg/m2; regular ovulatory cycles;
  • transvaginal ultrasound showing the presence of two ovaries with an antral follicle count (AFC) between 10 and 30 follicles;
  • affiliation to the national social security system.
  • Written informed consent was obtained from all participants

排除标准

  • - previous chemotherapy, ovarian surgery or endometrioma;

研究组 & 干预措施

Without injection group

Experimental

no injection used as priming

干预措施: hCG (Other)

Without injection group

Experimental

no injection used as priming

干预措施: GnRH a (Other)

hCG group

Active Comparator

hCG used as priming

干预措施: GnRH a (Other)

GnRHa group

Active Comparator

GnRH agonist used as priming

干预措施: No hormone (Other)

hCG group

Active Comparator

hCG used as priming

干预措施: No hormone (Other)

GnRHa group

Active Comparator

GnRH agonist used as priming

干预措施: hCG (Other)

结局指标

主要结局

total number of mature oocytes cryopreserved

时间窗: 4 days

Total number of mature oocytes obtained and cryopreserved after IVM

次要结局

  • number of COCS recovered(36 hours)
  • maturation rate(4 days)

研究者

发起方
Hôpital Jean Verdier
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael Grynberg

Professor

Hôpital Jean Verdier

研究点 (2)

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