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Comparison · NCT02152995-deaths

Cohort A (Iodine I-124 PET/CT, Trametinib, Iodine I-131) vs Cohort B (Iodine I-124 PET/CT, Trametinib, Iodine I-131): 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. Cohort A (Iodine I-124 PET/CT, Trametinib, Iodine I-131) vs Cohort B (Iodine I-124 PET/CT, Trametinib, Iodine I-131): deaths from any cause. Trial comparisons, record NCT02152995-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02152995-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 10.240.1150.434wilson
Risk in group 20.1110.01990.435wilson
Risk difference, group 1 minus group 20.129-0.2180.344newcombe hybrid score
Risk ratio, group 1 over group 22.160.315.6log
Odds ratio, group 1 over group 22.530.2624.5log
Number needed to harm, for one more death from any cause on Cohort A (Iodine I-124 PET/CT, Trametinib, Iodine I-131) than on Cohort B (Iodine I-124 PET/CT, Trametinib, Iodine I-131)7.76from 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 1Cohort A (Iodine I-124 PET/CT, Trametinib, Iodine I-131)
Patients with RAS gene mutations undergo iodine I-124 PET/CT on day 5 of week 1. Beginning day 6, patients receive trametinib PO daily for 4 weeks in the absence of disease progression or unacceptable toxicity. Patients undergo second iodine I-124 PET/CT on week 5. If I-124 PET/CT shows enough iodine absorption, patients may receive iodine I-131 PO and continue receiving trametinib for another 2 days. If I-124 shows that the thyroid is not absorbing iodine, patients have the option to be assigned to Cohort C.~Computed Tomography: Undergo iodine I-124 PET/CT~Iodine I 124: Undergo iodine I-124 PET/CT~Iodine I-131: Given PO~Laboratory Biomarker Analysis: Correlative studies~Pharmacodynamic Study: Correlative studies~Positron Emission Tomography: Undergo iodine I-124 PET/CT~Trametinib: Given PO
625EG000
Group 2Cohort B (Iodine I-124 PET/CT, Trametinib, Iodine I-131)
Patients without BRAF/RAS gene mutations undergo iodine I-124 PET/CT on day 5 of week 1. Beginning day 6, patients receive trametinib PO daily for 4 weeks in the absence of disease progression or unacceptable toxicity. Patients undergo second iodine I-124 PET/CT on week 5. If I-124 PET/CT shows enough iodine absorption, patients may receive iodine I-131 PO and continue receiving trametinib for another 2 days. If I-124 shows that the thyroid is not absorbing iodine, patients have the option to be assigned to Cohort C.~Computed Tomography: Undergo iodine I-124 PET/CT~Iodine I 124: Undergo iodine I-124 PET/CT~Iodine I-131: Given PO~Laboratory Biomarker Analysis: Correlative studies~Pharmacodynamic Study: Correlative studies~Positron Emission Tomography: Undergo iodine I-124 PET/CT~Trametinib: Given PO
19EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Up to 1 year

Source ClinicalTrials.gov

Trial

Title
Trametinib in Increasing Tumoral Iodine Incorporation in Patients With Recurrent or Metastatic Thyroid Cancer
NCT number
NCT02152995
Phases
PHASE2
Conditions
Metastatic Thyroid Gland Carcinoma, Poorly Differentiated Thyroid Gland Carcinoma, Recurrent Thyroid Gland Carcinoma, Refractory Thyroid Gland Carcinoma, Stage IV Thyroid Gland Follicular Carcinoma AJCC v7, Stage IV Thyroid Gland Papillary Carcinoma AJCC v7, Stage IVA Thyroid Gland Follicular Carcinoma AJCC v7, Stage IVA Thyroid Gland Papillary Carcinoma AJCC v7, Stage IVB Thyroid Gland Follicular Carcinoma AJCC v7, Stage IVB Thyroid Gland Papillary Carcinoma AJCC v7, Stage IVC Thyroid Gland Follicular Carcinoma AJCC v7, Stage IVC Thyroid Gland Papillary Carcinoma AJCC v7
Interventions
Computed Tomography, Iodine I 124, Iodine I-131, Laboratory Biomarker Analysis, Pharmacodynamic Study, Positron Emission Tomography, Trametinib
Lead sponsor
National Cancer Institute (NCI)
Results first posted
2022-12-28

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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