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Comparison · NCT05701007-95ea9343

Participants Diagnosed With mCSPC vs Participants Diagnosed With mCRPC: Number of Participants With de Novo Metastasis

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. Participants Diagnosed With mCSPC vs Participants Diagnosed With mCRPC: Number of Participants With de Novo Metastasis. Trial comparisons, record NCT05701007-95ea9343. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05701007-95ea9343

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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 10.5580.5240.593wilson
Risk in group 20.430.390.472wilson
Risk difference, group 1 minus group 20.1280.07430.181newcombe hybrid score
Risk ratio, group 1 over group 21.31.161.45log
Odds ratio, group 1 over group 21.681.352.09log
Number needed to treat, for one more participant with the outcome on Participants Diagnosed With mCSPC than on Participants Diagnosed With mCRPC7.795.5113.5from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Participants Diagnosed With mCSPCEligible participants with mCSPC and whose data were evaluated retrospectively.444795OG000
Group 2Participants Diagnosed With mCRPCEligible participants with mCRPC and whose data were evaluated retrospectively.240558OG001

Outcome

Type
PRIMARY
Title
Number of Participants With de Novo Metastasis
Description
The new metastasis was defined based on the prostate cancer diagnosis dates within 2 months from the index date. Index date for (i) mCSPC participants were defined as date for the first record of mPC (ii) mCRPC participants were defined as date for progression to metastatic castration resistant (if =3 months from castration-sensitive treatment initiation \[1st control usually at 3 months\], considered new CRPC).
Time frame
Within 2 months from index date; retrospective available data evaluated in this study for approximately 14 months
Population
Analysis population included all eligible participants whose data were included and observed for evaluation in the study.

Source ClinicalTrials.gov

Trial

Title
Real World Evidence Study on Metastatic Prostate Cancer in the Pirkanmaa Hospital District in Finland
NCT number
NCT05701007
Phases
Conditions
Metastatic Castration Sensitive Prostate Cancer (mCSPC), Metastatic Castration Resistant Prostate Cancer (mCRPC)
Interventions
abiraterone, enzalutamide, docetaxel, apalutamide, cabazitaxel, Radium-223, Lutetium-177, degarelix, goserelin, leuprorelin, triptorelin
Lead sponsor
Pfizer
Results first posted
2026-01-29

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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