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Recruiting Not applicable

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

NCT03830788 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2019-10-04
Last updated
2025-08-01

Condition(s) studied

Prostate Cancer

Investigational drug(s) / intervention(s)

Radiation by brachytherapyRadiation by SBRT

Radiation by brachytherapy: Brachytherapy by Iodine 125 delivering 144 Gy to the prostate

Radiation 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.

Study 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
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Main inclusion criteria * Biopsy proven prostate adenocarcinoma, * Low risk prostate cancer according to d'Amico (T1-T2a and PSA \<10 ng/ml, and Gleason score 6) or intermediate risk prostate cancer according d'Amico but excluding tumor with Gleason score 7 (4 + 3), * Indication of a curative treatment by brachytherapy validated in multidisciplinary consultation meeting, Main exclusion criteria * Androgen deprivation therapy, * Contraindication for prostate Iodine 125 brachytherapy (Prostate volume \> 50 cc, impossibility if general anesthesia). * Contraindication for Resonance Magnetic Imagery (RMI) (claustrophobia, pacemaker) * Participation to another research which could have an impact on the study treatment and the outcomes

Primary outcome measure(s)

  • Cost-utility analysis of SBRT compared to "standard" Iodine 125 brachytherapy — 3 years after treatment.
    The cost-utility analysis is expressed in cost per quality adjusted life year (QALY) gained.

Trial sites (20)

FacilityCityRegionStatus
Clinique Claude Bernard Albi France Not Yet Recruiting
ICO Paul Papin Angers France Recruiting
Institut Bergonié Bordeaux France Not Yet Recruiting
Polyclinique Bordeaux-Aquitaine Bordeaux France Recruiting
CLCC Georges-François Leclerc Dijon France Recruiting
Centre Amethys - Charlebourg - La Défense La Garenne-Colombes France Recruiting
Centre de Cobalthérapie Hartman Levallois-Perret France Not Yet Recruiting
CH Lyon Sud Lyon France Terminated
Institut régional du Cancer de Montpellier Montpellier France Not Yet Recruiting
Institut Curie Paris France Recruiting
Hôpital Lyon Sud Pierre-Bénite France Terminated
Institut Jean Godinot Reims France Not Yet Recruiting
Centre Eugene Marquis Rennes France Recruiting
Centre d'oncologie et de radiothérapie Saint Jean Saint-Doulchard France Recruiting
Institut de Cancérologie de l'Ouest - Site Gauducheau Saint-Herblain France Recruiting
Institut de Cancérologie Lucien Neuwirth Saint-Priest-en-Jarez France Not Yet Recruiting
Institut Claudius Régaud Toulouse France Not Yet Recruiting
CHU Tours - Hôpital Bretonneau Tours France Recruiting
Institut de Cancérologie de Lorraine Vandœuvre-lès-Nancy France Recruiting
Gustave Roussy Villejuif France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03830788 on ClinicalTrials.gov ↗ ← All trials in France