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

Launched by CENTER EUGENE MARQUIS · Feb 4, 2019

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Sbrt Brachytherapy Localized Low Risk And Intermediate Risk Prostate Cancer

ClinConnect Summary

The TEMPOS-GEniToUrinary Group (GETUG) study is examining two different treatments for prostate cancer to see which one is better at preventing erectile dysfunction. The trial involves 240 men with low to intermediate risk prostate cancer who are being treated with either brachytherapy or stereotactic body radiotherapy (SBRT). Brachytherapy involves placing radioactive seeds in the prostate, while SBRT uses targeted radiation in just a few sessions. The main goal of the study is to compare these two treatments not only in terms of their effectiveness but also their costs and impact on quality of life over five years.

To be eligible for this trial, participants need to have a confirmed diagnosis of prostate cancer that fits specific criteria, such as a low PSA level and a certain type of cancer cell score. They should not be undergoing other treatments that could interfere with the study. Men taking part in this research will be monitored for outcomes like erectile function and any side effects from the treatments, helping to determine the best approach for managing prostate cancer while minimizing complications. This study is important because it will help doctors and healthcare decision-makers understand which treatment is more cost-effective and beneficial for patients in the long term.

Gender

MALE

Eligibility criteria

  • 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

About Center Eugene Marquis

Center Eugene Marquis is a leading clinical research organization dedicated to advancing oncology through innovative research and patient-centered care. Located in Rennes, France, the center specializes in conducting high-quality clinical trials aimed at evaluating new therapies and improving treatment outcomes for cancer patients. With a multidisciplinary team of experienced professionals and state-of-the-art facilities, Center Eugene Marquis collaborates with academic institutions, pharmaceutical companies, and other stakeholders to foster groundbreaking discoveries and contribute to the global fight against cancer.

Locations

Rennes, , France

Paris, , France

Bordeaux, , France

Reims, , France

Albi, , France

Angers, , France

Villejuif, , France

Lyon, , France

Vandœuvre Lès Nancy, , France

Montpellier, , France

Toulouse, , France

Tours, , France

Saint Priest En Jarez, , France

Pierre Bénite, , France

Bordeaux, , France

Dijon, , France

Levallois Perret, , France

Saint Herblain, , France

La Garenne Colombes, , France

Saint Doulchard, , France

Patients applied

0 patients applied

Trial Officials

Renaud De Crevoisier, PR

Principal Investigator

Centre Eugène Marquis

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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