Phase III Study Comparing 3D Conformal Radiotherapy and Conformal Radiotherapy IMRT to Treat Endometrial Cancer
NCT ID: NCT01641497
Last Updated: 2017-07-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
TERMINATED
NA
26 participants
INTERVENTIONAL
2012-05-31
2016-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Intensity Modulated Radiation Therapy - Gyne Cancer (GY03.2)
NCT00188578
Adaptative Radiotherapy for Locally Advanced Cervical Cancer
NCT02937948
Study of SBRT Efficacy on Intra and Extra -Cranial Tumors or Metastasis in Pediatrics Population (SBRT Pediatrics)
NCT02013297
Intensity Modulated Radiotherapy (IMRT) for the Pelvis Post-Hysterectomy
NCT00508703
SBRT + Immunomodulating Systemic Therapy for Inoperable, Recurrent H&N
NCT03402737
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Some factors are involved in disease prognostic: age, geographical origin, physical status, tumor grade, tumor histology and probably biomarkers. Some studies demonstrated that advanced age is a negative prognostic factor due to higher relapse risk and higher specific mortality. Unfortunately, Incidence of endometrial cancer will probably increase in future due to aging of the occidental population.
Current treatment of endometrial cancer is based on post-operative radiation therapy: adjuvant brachytherapy or adjuvant external beam radiation therapy. However these techniques lead to serious toxicity (digestive toxicity, ileitis...) in elder patient. Consequently, pelvic radiation therapy is difficult to organize before 75 years and dangerous to perform after 80 years.
However a new technique called: Intensity-modulated radiation therapy (IMRT) can make the difference. IMRT is a new high precision radiotherapy technique probably well adapted for old people, with less toxicity than current radiotherapy.
Nevertheless, IMRT is not recognized as a standard radiation therapy procedure in France and Europe.
Thus, goal of TOMOGYN study is to compare the tolerance of old women (at least 70 years), with endometrial cancer, treated with external beam radiation therapy or IMRT.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
3D conformational radiotherapy
25 \* 1.8 Gy in 5 weeks (=45 Gy). 3D conformational radiation
3D conformational radiation
25 \* 1.8 Gy in 5 weeks (=45 Gy)
Intensity-Modulated Radiation Therapy
25 \* 1.8 Gy in 5 weeks (=45 Gy). IMRT
IMRT
25 \* 1.8 Gy in 5 weeks (=45 Gy)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
3D conformational radiation
25 \* 1.8 Gy in 5 weeks (=45 Gy)
IMRT
25 \* 1.8 Gy in 5 weeks (=45 Gy)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* post op pelvic radiotherapy
* age ≥ 70
* performance status ≤ 2
* MMSE ≥ 10
* life expectancy ≥ 3 months
* social security covered
* signed informed consent
Exclusion Criteria
* uterine sarcoma
* surgery not in accordance with recommendations of Inca
* previous uncontrolled or less than 5 years prior to diagnosis cancer
* cons-indication for radiotherapy
* diarrhea ≥ 3 per day
* pelvic lymph nodes \> 1cm not resected during staging
* previous sigmoid diverticulitis, crohn disease, systemic disease, ulcerative haemorrhagic, collagenosis, infectious peritonitis
* IMRT other than tomotherapy
* photon energy \< 10MV
* patient under guardianship
70 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Cancer Institute, France
OTHER_GOV
Centre Oscar Lambret
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Le Tinier Florence, MD
Role: PRINCIPAL_INVESTIGATOR
Centre Oscar Lambret
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Bergonie Institut
Bordeaux, , France
François Baclesse Center
Caen, , France
Oscar Lambret Center
Lille, , France
Centre Leon Berard
Lyon, , France
Institut Jean Godinot
Reims, , France
René Gauducheau Center
Saint-Herblain, , France
Paul Strauss Center
Strasbourg, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2011-A01543-38
Identifier Type: OTHER
Identifier Source: secondary_id
TOMOGYN - 1105
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.