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Phase 3 N=840 Randomized Quadruple-blind Treatment

Radiation Therapy With or Without Bicalutamide for Recurrent pT3N0 Prostate Cancer After Radical Prostatectomy

Prostate Cancer

Enrolled (actual)
840
Serious AEs
23.9%
Results posted
Aug 2017
Primary outcome: Primary: Overall Survival (12-year Rates Reported) — 71.3; 76.3 percentage of participants — p=0.020

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
bicalutamide (Drug); radiation therapy (Radiation); placebo (Drug)
Age
Pediatric, Adult, Older Adult
Sex
Male
Sponsor
Radiation Therapy Oncology Group
Primary completion
Aug 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Survival (12-year Rates Reported)
71.3; 76.3 0.020 sig
SECONDARY
Non-Prostate Cancer Death (12-year Rates Reported)
15.3; 17.9 0.289
SECONDARY
Second PSA Recurrence (12-year Rates Reported)
67.9; 44.0 <0.001 sig
SECONDARY
Third PSA Recurrence (12-year Rates Reported)
80.7; 84.2 0.213
SECONDARY
PSA Complete Response at End of Protocol Treatment
259; 360 <0.001 sig
SECONDARY
Distant Failure (12-year Rates Reported)
23.0; 14.5 0.002 sig
SECONDARY
Prostate Cancer Death (12-year Rates Reported)
13.4; 5.8 <0.001 sig
SECONDARY
Progression-free Survival (12-year Rates Reported)
23.9; 38.8 < 0.001 sig
SECONDARY
Grade 3+ Toxicity
17; 8; 73; 100 0.060

Summary

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Androgens can stimulate the growth of prostate cancer cells. Hormone therapy using bicalutamide may fight prostate cancer by reducing the production of androgens. It is not yet known if radiation therapy is more effective with or without bicalutamide for prostate cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy with or without bicalutamide in treating patients who have stage II or stage III prostate cancer and elevated prostate-specific antigen (PSA) levels following radical prostatectomy.

Eligibility Criteria

Conditions for Patient Eligibility:

  • The patient on entry will have no clinical evidence of disease by physical exam or by imaging studies. A positive ProstaScint scan alone without a confirmatory biopsy must not be used to exclude a patient. Eligible patients will be those who have undergone a radical prostatectomy (either retropubic or perineal) and pelvic lymphadenectomy (either open or laparoscopic) for carcinoma of the prostate, pathologic stage T3N0, or pT2 pN0 with positive inked resection margin, at least 12 weeks prior to study entry.
  • Pathological T2 patients without positive margins, who are also pathologic N0 with prostatic fossa/anastamosis biopsy at the time of rising PSA documenting recurrent cancer, are eligible.
  • At entry, the PSA must be between 0.2 and 4.0ng/ml, inclusive.
  • A post-prostatectomy radioisotopic bone scan which was done within 16 weeks prior to entry must reveal no evidence of metastatic disease.
  • Patient must be evaluated by both the radiation oncologist and the urologist prior to entry and judged to be a suitable candidate for radiation and hormonal therapy.
  • Patient must have Karnofsky performance status >= 80.
  • Patients must have a life expectancy in excess of 10 years.
  • Patients must have, within 6 weeks prior to entry, a hemoglobin (Hgb) of >=10 gm, a white blood cell (WBC) count of >= 4000 cells/ml3, a platelet count of >= 100,000 cells/ml3, a serum bilirubin 4.0ng/ml.
  • Patients with persistant urinary extravasation after prostatectomy.
  • Patients who have been previously treated with any hormonal therapy after prostatectomy.
  • Patients who have previously been treated with radiation therapy or biologic therapy for prostate cancer.
  • Karnofsky performance status 4 weeks after randomization.
  • Prior chemotherapy for any reason.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00002874). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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