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Comparison · NCT01027910-19bf97dc

Optional GCSF vs Mandatory GCSF: Rate of Progression-free Survival at 6 Months in Participants Who Received PCI-24781/Doxorubicin Combination Administration.

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. Optional GCSF vs Mandatory GCSF: Rate of Progression-free Survival at 6 Months in Participants Who Received PCI-24781/Doxorubicin Combination Administration. Trial comparisons, record NCT01027910-19bf97dc. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01027910-19bf97dc

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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 10.1670.03010.564wilson
Risk in group 20.4290.2140.674wilson
Risk difference, group 1 minus group 2-0.262-0.5430.189newcombe hybrid score
Risk ratio, group 1 over group 20.3890.05882.57log
Odds ratio, group 1 over group 20.2670.02432.92log
Number needed to treat, for one fewer participant with the outcome on Optional GCSF than on Mandatory GCSF3.82from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Optional GCSF16OG000
Group 2Mandatory GCSF614OG001

Outcome

Type
SECONDARY
Title
Rate of Progression-free Survival at 6 Months in Participants Who Received PCI-24781/Doxorubicin Combination Administration.
Description
Time frame
2 years
Population

Source ClinicalTrials.gov

Trial

Title
PCI-24781 in Combination With Doxorubicin to Treat Sarcoma
NCT number
NCT01027910
Phases
PHASE1, PHASE2
Conditions
Sarcoma
Interventions
PCI-24781, Doxorubicin, GCSF
Lead sponsor
Massachusetts General Hospital
Results first posted
2017-02-14

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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