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Comparison · NCT02839343-deaths

Arm 1 (mFOLFIRINOX + Surgery + FOLFOX) vs Arm 2 (mFOLFIRINOX + Radiation + Surgery + FOLFOXx): 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. Arm 1 (mFOLFIRINOX + Surgery + FOLFOX) vs Arm 2 (mFOLFIRINOX + Radiation + Surgery + FOLFOXx): deaths from any cause. Trial comparisons, record NCT02839343-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02839343-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 10.6360.5160.742wilson
Risk in group 20.4730.3470.602wilson
Risk difference, group 1 minus group 20.164-0.01320.328newcombe hybrid score
Risk ratio, group 1 over group 21.350.9641.88log
Odds ratio, group 1 over group 21.950.9414.05log
Number needed to harm, for one more death from any cause on Arm 1 (mFOLFIRINOX + Surgery + FOLFOX) than on Arm 2 (mFOLFIRINOX + Radiation + Surgery + FOLFOXx)6.11from 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 1Arm 1 (mFOLFIRINOX + Surgery + FOLFOX)
Patients receive 8 cycles of mFOLFIRINOX. One cycle is 14 days. mFOLFIRINOX consists of oxaliplatin, irinotecan, leucovorin and 5-FU. Patients undergo surgery and receive 4 cycles of FOLFOX 4-12 weeks after surgery. FOLFOX consists of oxaliplatin, leucovorin and 5-FU.
4266EG000
Group 2Arm 2 (mFOLFIRINOX + Radiation + Surgery + FOLFOXx)
Patients receive 7 cycles of mFOLFIRINOX. One cycle is 14 days. mFOLFIRINOX consists of oxaliplatin, irinotecan, leucovorin and 5-FU. Patients receive radiation therapy then undergo surgery and receive 4 cycles of FOLFOX 4-12 weeks after surgery. FOLFOX consists of oxaliplatin, leucovorin and 5-FU.
2655EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse events and Serious Adverse events were collected for 2 years and all cause mortality was collected for 4 years and 7 months.

Source ClinicalTrials.gov

Trial

Title
Combination Chemotherapy With or Without Hypofractionated Radiation Therapy Before Surgery in Treating Patients With Pancreatic Cancer
NCT number
NCT02839343
Phases
PHASE2
Conditions
Pancreatic Adenocarcinoma, Borderline Resectable Adenocarcinoma of the Head of the Pancrease
Interventions
radiation therapy, surgery, mFOLFIRINOX, FOLFOX
Lead sponsor
Alliance for Clinical Trials in Oncology
Results first posted
2022-05-24

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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