Genomic alterations, molecularly targeted therapy, and survival: a real-world Endometrial Cancer Molecularly Targeted

Angeles Alvarez Secord1, Victoria Bae-Jump2, Floor Backes3

  • 1Duke School of Medicine, Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Durham, NC, USA.

Abstract

Insights

Next-generation sequencing in advanced endometrial cancer frequently identifies actionable genomic alterations. Matched biologic therapies improved survival compared to chemotherapy in this patient cohort.

Area of Science:

  • Oncology
  • Genomics
  • Precision Medicine

Background:

  • Next-generation sequencing (NGS) and tumor testing are increasingly utilized for advanced/recurrent endometrial cancer.
  • The clinical impact of these molecular profiling approaches remains under investigation.

Purpose of the Study:

  • To determine the proportion of patients with actionable genomic alterations in advanced/recurrent endometrial cancer.
  • To assess if molecularly targeted therapy improves survival in metastatic endometrial cancer.

Main Methods:

  • A multidisciplinary consortium analyzed data from 967 patients across 12 centers.
  • Tumor testing, including NGS, and treatment decisions were based on physician recommendations.
  • Data included patient demographics, tumor characteristics, genomic alterations, protein expression, and survival outcomes.

Main Results:

  • 93.3% of patients underwent tumor testing, with 94.0% of those receiving NGS identifying at least one genomic alteration.
  • The most common alterations were PI3K (35.8%), TP53 (34.7%), and PTEN (26.5%) mutations.
  • 233 patients received matched biologic therapies, showing improved progression-free and overall survival compared to chemotherapy.

Conclusions:

  • Real-world data on genomic testing patterns and targeted therapy use were established for a diverse endometrial cancer cohort.
  • Matched biologic therapies demonstrated a survival benefit in advanced/recurrent endometrial cancer patients.