The potential role of GLP-1 receptor agonist targeting in fertility-sparing treatment in obese patients with endometrial malignant pathology: a call for research

Expert Rev Anticancer Ther. 2023 Apr;23(4):385-395. doi: 10.1080/14737140.2023.2194636. Epub 2023 Mar 28.

Abstract

Introduction: Most patients diagnosed with endometrial hyperplasia or cancer are obese. Obesity, along with polycystic ovarian syndrome (PCOS) and type-2 diabetes mellitus (T2DM), may act synergistically to increase risk of malignant endometrial pathology. Incidence of malignant endometrial pathology is increasing, particularly in reproductive aged women. In patients who desire future fertility, the levonorgestrel intrauterine device (LNG-IUD) is often utilized. If the first-line progestin therapy fails, there is not an effective second-line adjunct option. Moreover, pregnancy rates following fertility-sparing treatment are lower-than-expected in these patients.

Areas covered: This clinical opinion provides a summary of recent studies exploring risk factors for the development of malignant endometrial pathology including obesity, PCOS, and T2DM. Studies assessing efficacy of fertility-sparing treatment of malignant endometrial pathology are reviewed, and a potential new adjunct treatment approach to LNG-IUD is explored.

Expert opinion: There is an unmet-need for a personalized treatment approach in cases of first-line progestin treatment failure. Glucagon-like peptide 1 receptor agonists are a class of anti-diabetic agents, but may have a role in fertility-sparing treatment of obese patients with malignant endometrial pathology by reducing weight, decreasing inflammation, and decreasing insulin resistance; these changes may also improve chances of subsequent pregnancy. This hypothesis warrants further exploration.

Keywords: Endometrial cancer; GLP-1RA; endometrial intraepithelial neoplasm; fertility sparing; glucagon-like peptide 1 receptor agonist; insulin resistance; obesity; polycystic ovary syndrome; progestin therapy; type-2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Diabetes Mellitus, Type 2* / complications
  • Diabetes Mellitus, Type 2* / drug therapy
  • Endometrial Neoplasms* / drug therapy
  • Female
  • Fertility Preservation*
  • Glucagon-Like Peptide-1 Receptor / therapeutic use
  • Humans
  • Levonorgestrel / adverse effects
  • Obesity / complications
  • Obesity / drug therapy
  • Polycystic Ovary Syndrome* / chemically induced
  • Polycystic Ovary Syndrome* / complications
  • Polycystic Ovary Syndrome* / drug therapy
  • Pregnancy
  • Progestins / therapeutic use

Substances

  • Progestins
  • Glucagon-Like Peptide-1 Receptor
  • Levonorgestrel