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Comparison · NCT01720225-a2fae47b

Decitabine vs Azacitidine: Number of Participants Who Became Transfusion Independent

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: Number of Participants Who Became Transfusion Independent. Trial comparisons, record NCT01720225-a2fae47b. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01720225-a2fae47b

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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 10.3240.1960.485wilson
Risk in group 20.1580.05520.376wilson
Risk difference, group 1 minus group 20.166-0.08620.357newcombe hybrid score
Risk ratio, group 1 over group 22.050.6586.41log
Odds ratio, group 1 over group 22.560.62410.5log
Number needed to treat, for one more participant with the outcome on Decitabine than on Azacitidine6.01from 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.1237OG000
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.
319OG001

Outcome

Type
SECONDARY
Title
Number of Participants Who Became Transfusion Independent
Description
Participants who were transfusion dependent at baseline prior to starting therapy on the Decitabine or Azacitidine arm will be analyzed for transfusion independence. Transfusion independence defined as being transfusion-free for ≥8 consecutive weeks between the first dose and study treatment discontinuation.
Time frame
8 weeks
Population
Participants analyzed for Transfusion Independence must have been transfusion dependent at baseline. Thirty-seven participants in the Decitabine arm and nineteen participants in the Azacitidine arm where transfusion dependent prior to treatment on this study.

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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