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Comparison · NCT00002874-3f2a32b4

Bicalutamide vs Placebo: PSA Complete Response at End of Protocol Treatment

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Bicalutamide vs Placebo: PSA Complete Response at End of Protocol Treatment. Trial comparisons, record NCT00002874-3f2a32b4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00002874-3f2a32b4

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.9380.9090.958wilson
Risk in group 20.6890.640.734wilson
Risk difference, group 1 minus group 20.2490.1950.301newcombe hybrid score
Risk ratio, group 1 over group 21.361.271.46log
Odds ratio, group 1 over group 26.784.2510.8log
Number needed to treat, for one more participant with the outcome on Bicalutamide than on Placebo4.023.325.12from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1BicalutamideRadiation therapy (64.8 Gy) + bicalutamide (150 mg daily 2 years)360384OG001
Group 2PlaceboRadiation therapy (64.8 Gy) + placebo (daily 2 years)259376OG000

Outcome

Type
SECONDARY
Title
PSA Complete Response at End of Protocol Treatment
Description
Complete response is defined as a drop in PSA on protocol treatment to less than 0.2 ng/ml. Note that when the study opened many institutions could not detect PSA \< 05 ng/ml.
Time frame
End of protocol treatment, which is planned to last for two years
Population
Eligible patients who did not withdraw consent.

Source ClinicalTrials.gov

Trial

Title
Radiation Therapy With or Without Bicalutamide for Recurrent pT3N0 Prostate Cancer After Radical Prostatectomy
NCT number
NCT00002874
Phases
PHASE3
Conditions
Prostate Cancer
Interventions
bicalutamide, radiation therapy, placebo
Lead sponsor
Radiation Therapy Oncology Group
Results first posted
2017-08-18

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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