Status:

COMPLETED

Impact of Adjuvant Chemotherapy on the Quality of Life of Patients Treated for Stage II / III Endometrial Cancer

Lead Sponsor:

Centre Francois Baclesse

Conditions:

Endometrial Cancer

Chemotherapy Effect

Eligibility:

FEMALE

18+ years

Phase:

NA

Brief Summary

Through this study, The investigator believe to evaluate the impact in terms of overall quality of life of adjuvant chemotherapy in patients with locally advanced endometrial cancer at a distance from...

Detailed Description

Endometrial cancer is the fourth most common cancer in women in developed countries. The diagnosis is often made at a localized stage (67% of cases), making it a relatively good cancer prognosis with ...

Eligibility Criteria

Inclusion

  • For all patients:
  • Women over 18 years of age, with histologically confirmed histologic type 1 or type 2 endometrial adenocarcinoma, with FIGO postoperative II or III stage operated between 2011 and 2015, with at least 2 years of follow-up compared to the last course of chemotherapy;
  • Recommended surgery such as hysterectomy and bilateral salpingo-oophorectomy, non-mandatory surgical nodal staging;
  • Pelvic radiotherapy +/- lumbar-aortic irradiation, optional brachytherapy;
  • No recurrence of endometrial cancer at baseline;
  • Absence of evolutionary neurological antecedent (multiple sclerosis, neurodegenerative pathology ...);
  • Absence of progressive psychiatric pathology (i.e. psychiatric hospitalization, bipolar disorder, schizophrenia, personality disorders ...);
  • No opposition to the collection of data;
  • Patient deemed fit to answer a written questionnaire.
  • For the patient in the chemotherapy group - Chemotherapy after surgery that can be performed before or after radiotherapy

Exclusion

  • For all patients:
  • Sarcoma or carcinosarcoma;
  • Stage FIGO I or IV;
  • Macroscopic tumor residue after surgery;
  • Recurrence of endometrial cancer or diagnosis of any other cancerous pathology after diagnosis of endometrial cancer (except non-melanotic skin tumors with complete excision), within 5 years;
  • drug use;
  • Abuse of alcohol.
  • For the patient in the chemotherapy group
  • Chemotherapy before surgery;
  • Chemotherapy concomitant with radiotherapy
  • For the patient in the group without chemotherapy
  • \- Chemotherapy whether before or after surgery

Key Trial Info

Start Date :

March 29 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 28 2020

Estimated Enrollment :

51 Patients enrolled

Trial Details

Trial ID

NCT03466788

Start Date

March 29 2018

End Date

March 28 2020

Last Update

December 18 2025

Active Locations (5)

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Page 1 of 2 (5 locations)

1

Centre François Baclesse

Caen, France, 14076

2

Centre Oscar Lambret

Lille, France

3

Centre Eugène Marquis

Rennes, France

4

Centre Henri Becquerel

Rouen, France