Use of fertility drugs and risk of ovarian cancer

Curr Opin Obstet Gynecol. 2014 Jun;26(3):125-9. doi: 10.1097/GCO.0000000000000060.

Abstract

Purpose of review: The purpose of this review is to highlight recent research and insights into the relationship between fertility drug use and ovarian cancer risk.

Recent findings: Results from two large case-control studies provided further evidence that fertility drug use does not significantly contribute to risk of ovarian cancer among the majority of women when adjusting for known confounding factors. However, questions regarding the effect on certain subgroups, including long-term fertility drug users, women who remain nulligravid after fertility treatment, women with BRCA1 or BRCA2 mutations and borderline ovarian tumours, still remain. In addition, it may currently just be too early to determine whether there is an association between fertility drug use and ovarian cancer risk given that many of the exposed women are only now beginning to reach the ovarian cancer age range.

Summary: Whether use of fertility drugs increases the risk of ovarian cancer is an important question that requires further investigation, in particular given the large number of women utilizing fertility treatments. Fortunately, results from recent studies have been mainly reassuring. Large well designed studies with sufficient follow-up time are needed to further evaluate the effects of fertility treatments within subgroups defined by patient and tumour characteristics.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Adult
  • Case-Control Studies
  • Clomiphene / administration & dosage
  • Clomiphene / adverse effects*
  • Estrogens / administration & dosage
  • Estrogens / adverse effects*
  • Female
  • Fertility Agents, Female / administration & dosage
  • Fertility Agents, Female / adverse effects*
  • Genes, BRCA1 / drug effects
  • Genes, BRCA2 / drug effects
  • Gonadotropins / metabolism*
  • Humans
  • Infertility, Female / therapy
  • Mutation
  • Ovarian Neoplasms / chemically induced
  • Ovarian Neoplasms / epidemiology*
  • Ovarian Neoplasms / prevention & control
  • Ovulation Induction / adverse effects*
  • Ovulation Induction / methods
  • Parity
  • Pregnancy
  • Risk Factors
  • Time Factors

Substances

  • Estrogens
  • Fertility Agents, Female
  • Gonadotropins
  • Clomiphene