[Oncofertility and breast cancer]

Bull Cancer. 2019 Dec;106(12S1):S43-S52. doi: 10.1016/S0007-4551(20)30047-3.
[Article in French]

Abstract

Over the past decades, progresses in oncology have improved the recovery rates after numerous malignant diseases, including breast cancer, that strike young adults in childbearing age. Quality of life of young cancer survivors has become a major issue. However, anticancer therapies can have a detrimental impact on fertility. It is now well-established that all patients should receive information about the fertility risks associated with their cancer treatment and the fertility preservation options available. These techniques aim to limit the negative impact of chemotherapy on the ovaries or to preserve gametes before treatment. Currently, oocyte or embryo freezing after controlled ovarian hyperstimulation represents the most effective method for preserving female fertility. Over the past years innovative protocols of ovarian stimulation have been developed to enable breast cancer patients to undergo oocyte or embryo cryopreservation irrespective of the phase of the cycle or without exogenous follicle-stimulating hormone related increase in serum estradiol levels. When controlled ovarian hyperstimualtion cannot be implemented, other techniques such as cryopreservation of ovarian cortex, in vitro maturation or the use of GnRH agonists may be proposed. However, it is important to inform patients that all these fertility preservation techniques do not represent a guarantee of pregnancy.

Keywords: Congélation; Controlled ovarian; Cryoconservation; Fertility preservation; In vitro maturation; Maturation in vitro; Oocyte freezing; Ovarian tissue; Préservation; cryopreservation; de cortex ovarien; de la fertilité; ovocytaire Stimulation ovarienne; stimulation.

Publication types

  • Review

MeSH terms

  • Adult
  • Antineoplastic Agents / adverse effects
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Cryopreservation / methods
  • Embryo, Mammalian*
  • Female
  • Fertility Preservation / methods*
  • Genes, BRCA1
  • Genes, BRCA2
  • Humans
  • Male
  • Oocytes*
  • Ovary* / drug effects
  • Ovulation Induction / methods
  • Pregnancy
  • Quality of Life
  • Testis / drug effects
  • Young Adult

Substances

  • Antineoplastic Agents