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Comparison · NCT00527111-sae

Chemoradiotherapy Plus Cetuximab vs Chemoradiotherapy Alone: 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. Chemoradiotherapy Plus Cetuximab vs Chemoradiotherapy Alone: serious adverse events. Trial comparisons, record NCT00527111-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00527111-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 10.1490.08310.253wilson
Risk in group 20.08060.03490.175wilson
Risk difference, group 1 minus group 20.0686-0.04680.182newcombe hybrid score
Risk ratio, group 1 over group 21.850.675.11log
Odds ratio, group 1 over group 220.6436.22log
Number needed to harm, for one more participant with a serious adverse event on Chemoradiotherapy Plus Cetuximab than on Chemoradiotherapy Alone14.6from 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 1Chemoradiotherapy Plus CetuximabPelvic irradiation plus 5-fluorouracil plus cetuximab~Cetuximab~5-fluorouracil~Pelvic irradiation1067EG000
Group 2Chemoradiotherapy AlonePelvic irradiation plus 5-fluorouracil~5-fluorouracil~Pelvic irradiation562EG001

Harm

What it counts
Total, serious adverse events
Time frame
During the whole treatment period, up to 30 days following last dose.

Source ClinicalTrials.gov

Trial

Title
Pre-op Rectal ChemoRad +/- Cetuximab
NCT number
NCT00527111
Phases
PHASE2
Conditions
Rectal Cancer
Interventions
Cetuximab, 5-fluorouracil, Pelvic irradiation
Lead sponsor
US Oncology Research
Results first posted
2016-11-03

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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