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Role of Senescence in the Development of Endometrial Cancer

Not Applicable
Conditions
Endometrial Hyperplasia and Endometrial Cancers
Interventions
Genetic: Genetic analysis
Registration Number
NCT03338985
Lead Sponsor
CHU de Reims
Brief Summary

Several molecular studies showed chromosomal alterations in patients with endometrial cancer, with gains in 1q, 19p, 19q, 8q, 10q and 10p and loss of 4q, 16q and 18q. Several genes of interest have been identified (P53, PTEN, PIK3CA, ß-catenin, K-ras ...).

A study has already been carried out at the Reims University Hospital with inclusion of patients with endometrial cancer and patients with endometrial hyperplasia. It identified specific alterations of nosologic continuum of pathology and characterize areas of interest on the genome.

Detailed Description

make a pangenomic investigation of genetic abnormalities in atypical endometrial hyperplasia and endometrial cancers.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
140
Inclusion Criteria
  • patient with endometrial hyperplasia or endometrial cancer
  • patient consenting to participate to the study
  • patient enrolled in the national healthcare insurance program
  • patient older than 18 years
Exclusion Criteria
  • patient with neoadjuvant chemotherapy or radiotherapy prior to surgery

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Group "cases patients"Genetic analysispatients with endometrial hyperplasia or endometrial cancers
Primary Outcome Measures
NameTimeMethod
Genetic imbalancesDay 0

Genetic aberrations detected by comparative genomic hybridization (CGH arry)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Damien JOLLY

🇫🇷

Reims, France

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