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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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03830788
Acronym
TEMPOS
Enrollment
240
Registered
2019-02-05
Start date
2019-10-04
Completion date
2031-04-04
Last updated
2025-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

SBRT, brachytherapy, localized low-risk and intermediate risk prostate cancer

Brief 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.

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.

Sponsors

Center Eugene Marquis
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Cost-utility analysis of SBRT compared to standard Iodine 125 brachytherapy3 years after treatment.The cost-utility analysis is expressed in cost per quality adjusted life year (QALY) gained.

Secondary

MeasureTime frameDescription
Cost-utility analysis of SBRT compared to standard iodine-125 brachytherapy5 years after treatmentThe cost-utility analysis is expressed in cost per quality adjusted life year (QALY) gained.
Cost-utility analysis of avoided erectile dysfunction cost3 and 5 years after treatment

Countries

France

Contacts

Primary ContactMartine Gestin, PhD
m.gestin@rennes.unicancer.fr+33(0)299253036

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026