ClinicalTrials.Veeva

Menu

Reliability and Interest of Circulating Tumor DNA in Endometrial Cancers.

P

Poitiers University Hospital

Status

Completed

Conditions

Endometrial Cancer
Circulating Tumor DNA

Treatments

Diagnostic Test: One arm only

Study type

Interventional

Funder types

Other

Identifiers

NCT04456972
ENDOCIRC

Details and patient eligibility

About

The recent histo-prognostic molecular discoveries of the TCGA (The Cancer Genome Atlas) have shed new light on the classification of endometrial carcinomas.

After carrying out different types of high-throughput molecular analyzes on 373 endometrial carcinomas of different histological types, 4 major tumor subtypes could be identified, each with a different survival profile (the "ultra-mutated" group with POLE mutations, the "hypermuted" group with microsatellite instability (MSI), the "low number of copies" group, and the "high number of copies" group).

This histomolecular classification is not yet directly transposable to clinical practice and tumor genetic characteristics have not had any direct therapeutic impact to date.

The main objective of the study is to determine the concordance rate between molecular analysis of tumor tissue and that of cDNA in patients with endometrial cancer during treatment.

Enrollment

44 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histologically proven endometrial adenocarcinoma type I or type II.
  • With recent abdomino-pelvic imaging, less than 3 months old.
  • Tumor tissue sufficiently exploitable for research (> 20% of tumor cells)
  • Informed consent signed by the patient after clear and fair information about the study.
  • Free patient, without tutorship, curatorship or subordination.
  • Patient benefiting from a Social Security scheme or benefiting from it through a third person.
  • Patient not opposed to participating in the study.

Exclusion criteria

  • Histologies other than adenocarcinoma (sarcoma, leiomyosarcoma)
  • Linguistic or mental refusal or incapacity to understand and / or sign the informed consent
  • Patients benefiting from enhanced protection, namely: minors, persons deprived of their liberty by a judicial or administrative decision, persons staying in a health or social establishment, adults under legal protection.
  • Pregnant and / or lactating women

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

44 participants in 1 patient group

One arm only
Experimental group
Treatment:
Diagnostic Test: One arm only

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems