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Clinical Trials/NCT00223145
NCT00223145
Active, not recruiting
Phase 3

Randomized, Multicentre, Phase III Study in Patients with Intermediate-risk T1 T2 Prostate Adenocarcinomas, to Verify the Role of Six Months of Total Androgen Blockade for Two Dosage Levels of Prostate Radiation Therapy (70 Gy and 76 Gy) Versus Prostate Radiation Therapy Alone At 76 Gy

Abdenour Nabid1 site in 1 country600 target enrollmentDecember 2000

Overview

Phase
Phase 3
Intervention
Radiotherapy 70 Gy
Conditions
Prostate Cancer
Sponsor
Abdenour Nabid
Enrollment
600
Locations
1
Primary Endpoint
Interval before biochemical failure
Status
Active, not recruiting
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
December 2000
End Date
December 31, 2027
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
Abdenour Nabid
Responsible Party
Sponsor Investigator
Principal Investigator

Abdenour Nabid

Principal Investigator

Université de Sherbrooke

Eligibility Criteria

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.

Arms & Interventions

Arm 1

Androgen blockade for 6 months + Radiotherapy 70 Gy

Intervention: Radiotherapy 70 Gy

Arm 1

Androgen blockade for 6 months + Radiotherapy 70 Gy

Intervention: Androgen blockade

Arm 2

Androgen blockade for 6 months + Radiotherapy 76 Gy

Intervention: Radiotherapy 76 Gy

Arm 2

Androgen blockade for 6 months + Radiotherapy 76 Gy

Intervention: Androgen blockade

Arm 3

Radiotherapy alone with 76 Gy

Intervention: Radiotherapy 76 Gy

Outcomes

Primary Outcomes

Interval before biochemical failure

Time Frame: 10 years

Secondary Outcomes

  • Toxicity of irradiation(10 years)
  • Survival(10 years)

Study Sites (1)

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