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Comparison · NCT00006237-sae

Interferon vs Biochemotherapy: 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. Interferon vs Biochemotherapy: serious adverse events. Trial comparisons, record NCT00006237-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00006237-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 10.01040.002850.037wilson
Risk in group 20.02160.008440.0543wilson
Risk difference, group 1 minus group 2-0.0113-0.04480.0185newcombe hybrid score
Risk ratio, group 1 over group 20.4790.08882.59log
Odds ratio, group 1 over group 20.4740.08572.62log
Number needed to treat, for one fewer participant with a serious adverse event on Interferon than on Biochemotherapy88.8from 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 1Interferoninterferon alfa2193EG000
Group 2Biochemotherapycisplatin, dacarbazine, interleukin-2, interferon alfa SC, filgrastim4185EG001

Harm

What it counts
Total, serious adverse events
Time frame
While the patient is on treatment until resolution of acute toxicities with maximum grade reported

Source ClinicalTrials.gov

Trial

Title
S0008: Chemotherapy Plus Biological Therapy in Treating Patients With Melanoma
NCT number
NCT00006237
Phases
PHASE3
Conditions
Melanoma (Skin)
Interventions
interleukin-2, filgrastim, interferon alfa, cisplatin, dacarbazine, vinblastine
Lead sponsor
SWOG Cancer Research Network
Results first posted
2012-09-19

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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