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

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

26 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-05-31

Study Completion Date

2016-10-31

Brief Summary

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Comparison of radiotherapy tolerance (two types of radiotherapy) for patients over 70 years with a endometrial cancer.

Detailed Description

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Endometrial cancer is the most common form of gynecological cancer in France with 6560 new cases in 2010. Endometrial cancers occurs generally after menopause but are sometimes diagnosticated before 40 years. The 5 years Overall survival of endometrial cancer is 76% (95% for non locally advanced or non metastatic disease).

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

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Endometrial Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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3D conformational radiotherapy

25 \* 1.8 Gy in 5 weeks (=45 Gy). 3D conformational radiation

Group Type ACTIVE_COMPARATOR

3D conformational radiation

Intervention Type RADIATION

25 \* 1.8 Gy in 5 weeks (=45 Gy)

Intensity-Modulated Radiation Therapy

25 \* 1.8 Gy in 5 weeks (=45 Gy). IMRT

Group Type EXPERIMENTAL

IMRT

Intervention Type RADIATION

25 \* 1.8 Gy in 5 weeks (=45 Gy)

Interventions

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3D conformational radiation

25 \* 1.8 Gy in 5 weeks (=45 Gy)

Intervention Type RADIATION

IMRT

25 \* 1.8 Gy in 5 weeks (=45 Gy)

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* endometrial adenocarcinoma histologically proven
* post op pelvic radiotherapy
* age ≥ 70
* performance status ≤ 2
* MMSE ≥ 10
* life expectancy ≥ 3 months
* social security covered
* signed informed consent

Exclusion Criteria

* type I stade IAGI and stade IAGIII without myometer infiltration, stade IIIc2 and IV adenocarcinoma
* 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
Minimum Eligible Age

70 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute, France

OTHER_GOV

Sponsor Role collaborator

Centre Oscar Lambret

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Le Tinier Florence, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Oscar Lambret

Locations

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Bergonie Institut

Bordeaux, , France

Site Status

François Baclesse Center

Caen, , France

Site Status

Oscar Lambret Center

Lille, , France

Site Status

Centre Leon Berard

Lyon, , France

Site Status

Institut Jean Godinot

Reims, , France

Site Status

René Gauducheau Center

Saint-Herblain, , France

Site Status

Paul Strauss Center

Strasbourg, , France

Site Status

Countries

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France

Other Identifiers

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2011-A01543-38

Identifier Type: OTHER

Identifier Source: secondary_id

TOMOGYN - 1105

Identifier Type: -

Identifier Source: org_study_id

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