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Comparison · NCT00088413-c0b17d20

Breast Cancer Cohort vs Ovarian Cancer Cohort: Number of Participants With an Positive Immune Response to Carcinoembryonic Antigen (CEA) Peptide and/or Protein in the Breast Cancer and Ovarian Cancer Cohorts Post Vaccination

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. Breast Cancer Cohort vs Ovarian Cancer Cohort: Number of Participants With an Positive Immune Response to Carcinoembryonic Antigen (CEA) Peptide and/or Protein in the Breast Cancer and Ovarian Cancer Cohorts Post Vaccination. Trial comparisons, record NCT00088413-c0b17d20. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00088413-c0b17d20

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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 10.3330.06150.792wilson
Risk in group 20.50.09450.905wilson
Risk difference, group 1 minus group 2-0.167-0.6550.446newcombe hybrid score
Risk ratio, group 1 over group 20.6670.08035.54log
Odds ratio, group 1 over group 20.50.012819.6log
Number needed to treat, for one fewer participant with the outcome on Breast Cancer Cohort than on Ovarian Cancer Cohort6from 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 1Breast Cancer CohortPatients with evaluable, metastatic breast cancer who have failed or not a candidate for standard therapy.13OG000
Group 2Ovarian Cancer CohortPatients with evaluable, metastatic ovarian cancer who have failed or not a candidate for standard therapy.12OG001

Outcome

Type
SECONDARY
Title
Number of Participants With an Positive Immune Response to Carcinoembryonic Antigen (CEA) Peptide and/or Protein in the Breast Cancer and Ovarian Cancer Cohorts Post Vaccination
Description
Immune response in human leukocyte antigens (HLA)-A2 positive patients to carcinoembryonic antigen (CEA) was assessed by enzyme-linked immunospot assay (ELISPOT) analysis. A positive immune response was defined as a \>2x fold increase in the number of interferon gamma producing cells.
Time frame
post vaccination (up to Day 84)
Population
Only 3 Breast Cancer and 2 Ovarian Cancer patients had enough blood collected to perform enzyme-linked immunospot (ELISPOT) analysis.

Source ClinicalTrials.gov

Trial

Title
PANVAC-V and PANVAC-F Vaccines Plus Sargramostim to Treat Advanced Cancer
NCT number
NCT00088413
Phases
PHASE1, PHASE2
Conditions
Adenocarcinoma, Colorectal Cancer, Ovarian Cancer, Breast Cancer
Interventions
PANVAC-V, PANVAC-F, Sargramostim (GM-CSF, Leukine)
Lead sponsor
National Cancer Institute (NCI)
Results first posted
2019-04-16

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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