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Comparison · NCT00923117-sae

Bevacizumab Resistant Patients vs Bevacizumab Naive Patients: serious adverse events

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. Bevacizumab Resistant Patients vs Bevacizumab Naive Patients: serious adverse events. Trial comparisons, record NCT00923117-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00923117-sae

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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 10.3640.2380.511wilson
Risk in group 20.3020.1860.451wilson
Risk difference, group 1 minus group 20.0613-0.1330.249newcombe hybrid score
Risk ratio, group 1 over group 21.20.6612.19log
Odds ratio, group 1 over group 21.320.5393.23log
Number needed to harm, for one more participant with a serious adverse event on Bevacizumab Resistant Patients than on Bevacizumab Naive Patients16.3from 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 1Bevacizumab Resistant PatientsPatients who had tumor progression while treated with bevacizumab.1644EG000
Group 2Bevacizumab Naive PatientsPatients with progressive tumor who have not been treated with bevacizumab.1343EG001

Harm

What it counts
Total, serious adverse events
Time frame

Source ClinicalTrials.gov

Trial

Title
Sunitinib to Treat Recurrent Brain Cancer
NCT number
NCT00923117
Phases
PHASE2
Conditions
Glioblastoma Multiforme, Malignant Gliomas, Anaplastic Gliomas
Interventions
Sutent (sunitinib)
Lead sponsor
National Cancer Institute (NCI)
Results first posted
2013-06-25

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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