Study on the Role of Hormonal Treatment for Two Dosage Levels of Prostate Radiation Therapy Versus Prostate Radiation Therapy Alone

Phase 3

Active, not recruiting

• Conditions: Prostate Cancer
• Interventions: Radiation: Radiotherapy 76 Gy; Radiation: Radiotherapy 70 Gy; Drug: Androgen blockade

• Registration Number: NCT00223145
• Lead Sponsor: Abdenour Nabid

Brief Summary

The hypothesis of the proposed study would be that, due to the six months of total androgen blockade, which would include neoadjuvant hormonal therapy for four months and concomitant hormonal therapy for two months with irradiation, the investigators could reduce local failure rates for these two dosage levels, namely 70 Gy and 76 Gy. Since increasing the dose to the prostate also seems to reduce local relapse rates, the results of the two hormonal therapy groups would be compared with the results of prostate irradiation at doses of 76 Gy. This study would verify the possibility of compensating a six Gy dosage increase of radiation therapy with six months of hormonal therapy between the 70 Gy and 76 Gy groups who received hormonal therapy, and also match these results with a dose escalation to the prostate of 76 Gy. In the future, this could result in more therapeutic choices, such as reducing the doses of radiation therapy and, consequently, its related complications, if hormonal therapy proves to be beneficial; or rather, to continue in the direction of dose escalation for this intermediate-risk patient group, everything being correlated to the side effects of hormonal therapy and irradiation.

Detailed Description

Not available

Study Timeline

• Study Start: 2000-12
• Study First Submitted: 2005-09-13
• Study First Submitted QC: 2005-09-15
• Study First Posted: 2005-09-22
• Status Verified: 2025-01
• Last Update Submitted: 2025-01-22
• Last Update Posted: 2025-01-27
• Primary Completion: 2026-12-31
• Study Completion: 2027-12-31

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: Male
• Target Recruitment: 600

Inclusion Criteria

• Patients with stage T1 or T2 untreated adenocarcinoma of the prostate, with a Gleason score that is less than or equal to 6, as well as a prostate-specific antigen (PSA) between 10-20 (intermediate risk) or patients with stage T1 or T2 untreated adenocarcinoma of the prostate, with a Gleason score that is equal to 7, as well as a PSA equal to or less than 20 (intermediate risk).
• Performance status score of 0-1
• Patients must sign a consent form before starting the study.
• No evidence of regional disease
• Patients with a previous history of cancer are eligible on the condition that they have been disease-free for more than five years.
• Non-invasive epidermoid cancers of the skin are eligible.
• The patient must be available for treatments and follow-up visits.
• No evidence of metastatic disease, confirmed by a negative bone scan.

Exclusion Criteria

• Severe medical or psychiatric problems that may compromise study compliance
• Chronic hepatic disease; abnormal hepatic function, i.e. aspartate aminotransferase and alanine aminotransferase > 1.5 times the upper normal limit.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Arm 3	Radiotherapy 76 Gy	Radiotherapy alone with 76 Gy
Arm 1	Radiotherapy 70 Gy	Androgen blockade for 6 months + Radiotherapy 70 Gy
Arm 1	Androgen blockade	Androgen blockade for 6 months + Radiotherapy 70 Gy
Arm 2	Radiotherapy 76 Gy	Androgen blockade for 6 months + Radiotherapy 76 Gy
Arm 2	Androgen blockade	Androgen blockade for 6 months + Radiotherapy 76 Gy

Primary Outcome Measures

Name	Time	Method
Interval before biochemical failure	10 years

Secondary Outcome Measures

Name	Time	Method
Toxicity of irradiation	10 years
Survival	10 years

Trial Locations

Locations (1)

Centre de Recherche Clinique du CHUS; 🇨🇦 Sherbrooke, Quebec, Canada