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Comparison · NCT02908477-deaths

De-escalated Adjuvant Radiation Therapy (DART) vs Standard of Care Treatment (SOC): 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. De-escalated Adjuvant Radiation Therapy (DART) vs Standard of Care Treatment (SOC): deaths from any cause. Trial comparisons, record NCT02908477-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02908477-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 10.01470.004040.052wilson
Risk in group 20.09780.05230.176wilson
Risk difference, group 1 minus group 2-0.0831-0.162-0.0243newcombe hybrid score
Risk ratio, group 1 over group 20.150.03320.68log
Odds ratio, group 1 over group 20.1380.0290.653log
Number needed to treat, for one fewer death from any cause on De-escalated Adjuvant Radiation Therapy (DART) than on Standard of Care Treatment (SOC)126.1941.2from the risk difference interval

Groups2

Group 2 names the comparator: standard of care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1De-escalated Adjuvant Radiation Therapy (DART)Docetaxel: 15 mg/m2. Experimental arm only.2136EG000
Group 2Standard of Care Treatment (SOC)Cisplatin: 40 mg/m2. Standard arm only.992EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse events were collected over 2 years and mortality was collected over 5 years

Source ClinicalTrials.gov

Trial

Title
Evaluation of De-escalated Adjuvant Radiation Therapy for Human Papillomavirus (HPV)-Associated Oropharynx Cancer
NCT number
NCT02908477
Phases
PHASE3
Conditions
Oropharynx Cancer
Interventions
Adjuvant Radiation Therapy, Docetaxel, Cisplatin
Lead sponsor
Mayo Clinic
Results first posted
2024-04-08

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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