RecruitingNot ApplicableNCT03830788

Erectile Dysfunction in Good Prognosis Prostate Cancer : Comparison Between Brachytherapy and Stereotactic Body Radiotherapy

Erectile Dysfunction in Good Prognosis Prostate Cancer: a Phase III Medico-economic Study Comparing Brachytherapy to Stereotactic Body Radiotherapy


Sponsor

Center Eugene Marquis

Enrollment

240 participants

Start Date

Oct 4, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

The TEMPOS-GEniToUrinary Group (GETUG) study is a multicenter, medico-economic study comparing brachytherapy to SBRT in low and intermediate risk prostate cancer, particularly focused on the issue of erectile dysfunction. A total of 240 potent patients are randomized in two arms. The experimental arm consists of SBRT delivering 7.25 Gy per fraction, in five fractions, corresponding to a total dose of 36.25 Gy to the prostate. The control arm consists of brachytherapy by Iodine 125 delivering 144 Gy to the prostate. The main objective of this health economics study is to perform a cost-utility analysis of SBRT compared to "standard" Iodine 125 brachytherapy in low-risk prostate cancer, 3 years after treatment. The endpoint is the Incremental Cost-Utility Ratio (ICUR) between SBRT and brachytherapy as primary criterion, expressed in cost per quality adjusted life year (QALY) gained. Cost-effectiveness analyses are performed as secondary objective with Incremental Cost-Effectiveness Ratios (ICERs) expressed as cost per erectile dysfunction avoided and cost per Life Year Gained. A long term evaluation is also performed, including a cost-utility, cost-effectiveness and budget impact analysis at 5 years, a comprehensive assessment of the erectile dysfunction up to 5 years after treatment, an evaluation of acute and late genito-urinary (GU) and Gastro-Intestinal (GI) toxicities, and of quality of life up to 5 years after treatment. Eight patients/year/center are expected to be recruited in 2 years in about twenty participating centers. In total, to our knowledge, this study will be the first health economic evaluation which compares SBRT versus Iodine 125 brachytherapy in low risk and intermediate risk prostate cancer. Both cost-utility and cost-effectiveness analyses will also provide useful and complementary information to decision makers in order (i) to recommend the best strategy to adopt; (ii) to estimate the budget impact on the French National Health Insurance of the generalization of the cost-effective strategy. Finally, this study will allow to assess and compare accurately the erectile dysfunction after both treatment modalities.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two types of internal radiation (brachytherapy) treatments for early-stage prostate cancer that has a good prognosis, to see which approach has fewer side effects on sexual function — specifically whether a focal (targeted to one area) approach works as well as the whole-prostate approach. **You may be eligible if...** - You have been diagnosed with prostate adenocarcinoma confirmed by biopsy - Your cancer is low-risk (early stage, low PSA, Gleason score 6) or intermediate-risk (but not the more aggressive Gleason 4+3 pattern) - Your treatment team has recommended brachytherapy (internal radiation seed implant) as a curative option - You are able to have general anesthesia and MRI scans **You may NOT be eligible if...** - You are currently receiving hormone therapy (androgen deprivation) - You have a prostate that is too large for brachytherapy (over 50cc) - You have a pacemaker or severe claustrophobia that prevents MRI - You are enrolled in another study that could affect treatment outcomes Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONRadiation by brachytherapy

Brachytherapy by Iodine 125 delivering 144 Gy to the prostate

RADIATIONRadiation by SBRT

SBRT delivers 7.25 Gy per fraction, in five fractions, corresponding to a total dose of 36.25 Gy to the prostate. Fiducials are implanted in the prostate.


Locations(20)

Clinique Claude Bernard

Albi, France

ICO Paul Papin

Angers, France

Institut Bergonié

Bordeaux, France

Polyclinique Bordeaux-Aquitaine

Bordeaux, France

CLCC Georges-François Leclerc

Dijon, France

Centre Amethys - Charlebourg - La Défense

La Garenne-Colombes, France

Centre de Cobalthérapie Hartman

Levallois-Perret, France

CH Lyon Sud

Lyon, France

Institut régional du Cancer de Montpellier

Montpellier, France

Institut Curie

Paris, France

Hôpital Lyon Sud

Pierre-Bénite, France

Institut Jean Godinot

Reims, France

Centre Eugene Marquis

Rennes, France

Centre d'oncologie et de radiothérapie Saint Jean

Saint-Doulchard, France

Institut de Cancérologie de l'Ouest - Site Gauducheau

Saint-Herblain, France

Institut de Cancérologie Lucien Neuwirth

Saint-Priest-en-Jarez, France

Institut Claudius Régaud

Toulouse, France

CHU Tours - Hôpital Bretonneau

Tours, France

Institut de Cancérologie de Lorraine

Vandœuvre-lès-Nancy, France

Gustave Roussy

Villejuif, France

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NCT03830788


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