Excellent concordance of the molecular classification between preoperative biopsy and final hysterectomy in endometrial carcinoma

Gynecol Oncol. 2024 Nov:190:139-145. doi: 10.1016/j.ygyno.2024.08.016. Epub 2024 Aug 26.

Abstract

Objective: The 2023 International Federation of Gynecology and Obstetrics classification with molecular classification shows superior discriminatory ability compared to staging systems lacking molecular data. However, the accuracy of endometrial biopsy data in molecular classification remains uncertain. This study aimed to assess the concordance of molecular classifications between preoperative biopsy and hysterectomy to predict prognosis before surgical staging.

Methods: Endometrial biopsies and corresponding hysterectomy specimens were collected at the National Cancer Center Hospital between 2012 and 2023. Immunohistochemistry for p53 and mismatch repair (MMR) proteins and next-generation sequencing of all exons of polymerase epsilon (POLE) were performed. Given the limited number of POLE mut cases in prior studies, we prepared a POLE mut-enriched cohort. Cohen's kappa estimates were used to determine concordance for molecular and clinicopathological subgroup assignments.

Results: Among 70 patients classified into four molecular subtype groups, 33 exhibited POLE mutations, 15 showed loss of MMR protein expression, 13 had p53-abnormality, and 9 had no specific molecular profile. Concordance between biopsy and hysterectomy specimens was 100% (κ = 1.000). In contrast, histological types and grades between biopsy and surgical specimens showed moderate and substantial agreement (κ = 0.420 and κ = 0.780, respectively).

Conclusions: Molecular subtypes were completely consistent with those derived from surgical specimens, demonstrating high concordance between preoperative and postoperative molecular classifications. This suggests that endometrial biopsies could reliably predict prognosis. Future studies should investigate how biopsy-based molecular profiling influences treatment planning and patient outcomes.

Keywords: Concordance rate; Endometrial biopsy; Endometrial cancer; Molecular classification.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biopsy
  • DNA Mismatch Repair
  • DNA Polymerase II* / genetics
  • Endometrial Neoplasms* / classification
  • Endometrial Neoplasms* / genetics
  • Endometrial Neoplasms* / pathology
  • Endometrial Neoplasms* / surgery
  • Female
  • Humans
  • Hysterectomy*
  • Middle Aged
  • Mutation
  • Neoplasm Staging
  • Poly-ADP-Ribose Binding Proteins / genetics
  • Tumor Suppressor Protein p53 / genetics

Substances

  • DNA Polymerase II
  • Tumor Suppressor Protein p53
  • Poly-ADP-Ribose Binding Proteins
  • POLE protein, human