Hormone receptor expression patterns define clinically meaningful subgroups of endometrioid ovarian carcinoma

Gynecol Oncol. 2019 Nov;155(2):318-323. doi: 10.1016/j.ygyno.2019.09.001. Epub 2019 Sep 5.

Abstract

Background: Numerous studies have investigated the association between hormone receptor expression and clinical outcome in ovarian carcinoma (OC); however, these have largely focussed on serous OCs, with few studies reporting specifically on endometrioid OCs (EnOC). Where analyses have been stratified by histotype, expression has been assessed using the percentage of positive tumor cells, without accounting for nuclear expression intensity.

Methods: Here we assess the expression levels of progesterone receptor (PR), estrogen receptor alpha (ER) and androgen receptor (AR) using histoscore - a nuclear scoring method incorporating both proportion of positive cells and the intensity of nuclear staining - across a cohort of 107 WT1 negative EnOCs.

Results: Hierarchical clustering by PR, ER and AR histoscores identified four EnOC subgroups (PR+/ER+, PR+/ER-, PR-/ER+ and PR-/ER-). EnOC patients in the PR+/ER+ and PR+/ER- groups displayed favorable outcome (multivariable HR for disease-specific survival 0.05 [0.01-0.35] and 0.05 [0.00-0.51]) compared to the PR-/ER+ group. Ten-year survival for stage II PRhigh and PRlow cases was 94.1% and 42.4%. ERhigh EnOC patients (PR+/ER+, PR-/ER+) had higher body mass index compared to ERlow cases (P = 0.015) and high grade serous OC patients (P < 0.001).

Conclusion: These data demonstrate that endometrioid OC cases with high PR expression display markedly favorable outcome. Stage II EnOCs with high PR expression represent potential candidates for de-escalation of first-line therapy. Future work should seek to characterise the sensitivity of PR and ER positive EnOCs to endocrine therapy.

Keywords: Androgen receptor; Body mass index; Endometrioid ovarian carcinoma; Estrogen receptor; Ovarian cancer; Progesterone receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Body Mass Index
  • Carcinoma, Endometrioid / metabolism
  • Carcinoma, Endometrioid / mortality*
  • Estrogen Receptor alpha / metabolism*
  • Female
  • Humans
  • Middle Aged
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / mortality*
  • Receptors, Androgen / metabolism*
  • Receptors, Progesterone / metabolism*
  • Retrospective Studies

Substances

  • AR protein, human
  • ESR1 protein, human
  • Estrogen Receptor alpha
  • Receptors, Androgen
  • Receptors, Progesterone