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Comparison · NCT01720225-deaths

Decitabine vs Azacitidine: deaths from any cause

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. Decitabine vs Azacitidine: deaths from any cause. Trial comparisons, record NCT01720225-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01720225-deaths

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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 10.09590.04720.185wilson
Risk in group 20.050.01380.165wilson
Risk difference, group 1 minus group 20.0459-0.0790.142newcombe hybrid score
Risk ratio, group 1 over group 21.920.4188.8log
Odds ratio, group 1 over group 22.020.39810.2log
Number needed to harm, for one more death from any cause on Decitabine than on Azacitidine21.8from 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 1DecitabinePatients randomized to receive Decitabine 20 mg/m2 by vein daily for 3 days (days 1-3) every 28 days.~Decitabine: 20 mg/m2 by vein daily for 3 days (days 1-3) every 28 days.773EG000
Group 2Azacitidine
Patients randomized to receive Azacitidine 75 mg/m2 subcutaneously or by vein daily for 3 days (days 1-3) every 28 days.~Azacitidine: 75 mg/m2 subcutaneously or by vein daily for 3 days (days 1-3) every 28 days.
240EG001

Harm

What it counts
Total, all-cause mortality
Time frame
3 years, 3 months

Source ClinicalTrials.gov

Trial

Title
Decitabine Versus Azacitidine in Myelodysplastic Syndrome Patients With Low and Intermediate-1 Risk
NCT number
NCT01720225
Phases
PHASE2
Conditions
Leukemia
Interventions
Decitabine, Azacitidine
Lead sponsor
M.D. Anderson Cancer Center
Results first posted
2020-12-24

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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