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Comparison · NCT01466036-sae

Metastatic or Unresectable PNET vs Metastatic or Unresectable Carcinoid: 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. Metastatic or Unresectable PNET vs Metastatic or Unresectable Carcinoid: serious adverse events. Trial comparisons, record NCT01466036-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01466036-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 10.750.5310.888wilson
Risk in group 20.5850.4340.722wilson
Risk difference, group 1 minus group 20.165-0.09350.37newcombe hybrid score
Risk ratio, group 1 over group 21.280.8931.84log
Odds ratio, group 1 over group 22.130.6486.97log
Number needed to harm, for one more participant with a serious adverse event on Metastatic or Unresectable PNET than on Metastatic or Unresectable Carcinoid6.07from 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 1Metastatic or Unresectable PNETpatients were stratified by primary tumor site but received the same treatment. This cohort had pancreatic neuroendocrine tumors.~Cabozantinib: 60 mg QD orally in cycles of 28 days1520EG000
Group 2Metastatic or Unresectable CarcinoidPatients were stratified by primary tumor site but received the same treatment. This cohort had advanced or metastatic carcinoid tumor.~Cabozantinib: 60 mg QD orally in cycles of 28 days2441EG001

Harm

What it counts
Total, serious adverse events
Time frame
Participants were followed for AEs and SAEs starting from the first dose of study treatment, throughout the study, and through 30 days from the last study treatment. Median treatment duration was 8 cycles for the Carcinoid cohort and 12.5 cycles for the PNET cohort. Patients were followed for AEs during the time on treatment plus 30 days (median of 9.6 months). Participants were followed for All-Cause Mortality for longer (median 89.1 months).

Source ClinicalTrials.gov

Trial

Title
Cabozantinib in Advanced Pancreatic Neuroendocrine and Carcinoid Tumors
NCT number
NCT01466036
Phases
PHASE2
Conditions
Carcinoid Tumor, Pancreatic Neuroendocrine Tumor
Interventions
Cabozantinib
Lead sponsor
Dana-Farber Cancer Institute
Results first posted
2023-07-20

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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