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Trial · NCT03258554

Results by group29

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Dose-limiting Toxicity (DLT) [Lead-in Phase](Lead-in) RT + Durvalumab0Participants
Progression-free Survival (Percentage of Participants Alive Without Progression) [Phase II Primary]RT + Cetuximab63.795% Confidence Interval 51.3 to 76.1percentage of participants
Progression-free Survival (Percentage of Participants Alive Without Progression) [Phase II Primary]RT + Durvalumab50.695% Confidence Interval 41.5 to 59.8percentage of participants
Overall Survival (Percentage of Participants Alive) [Originally Phase III Primary / Now Phase II Secondary]RT+ Cetuximab77.595% Confidence Interval 66.7 to 88.3percentage of participants
Overall Survival (Percentage of Participants Alive) [Originally Phase III Primary / Now Phase II Secondary]RT + Durvalumab69.395% Confidence Interval 60.8 to 77.8percentage of participants
Locoregional Failure (Percentage of Participants With Locoregional Failure)RT+ Cetuximab18.995% Confidence Interval 10.0 to 29.9percentage of participants
Locoregional Failure (Percentage of Participants With Locoregional Failure)RT + Durvalumab31.395% Confidence Interval 23.0 to 40.0percentage of participants
Distant Metastasis (Percentage of Participants With Distant Metastasis)RT+ Cetuximab12.195% Confidence Interval 5.3 to 22.0percentage of participants
Distant Metastasis (Percentage of Participants With Distant Metastasis)RT + Durvalumab9.595% Confidence Interval 5.0 to 15.7percentage of participants
Competing Mortality (Percentage of Participants Who Died Due to Causes Other Than Study Cancer)RT+ Cetuximab5.395% Confidence Interval 1.4 to 13.4percentage of participants
Competing Mortality (Percentage of Participants Who Died Due to Causes Other Than Study Cancer)RT + Durvalumab10.595% Confidence Interval 5.7 to 17.0percentage of participants
Percentage of Participants With Complete or Partial Response at 4-month Scan Determined by Response Evaluation Criteria in Solid Tumors (RECIST) v. 1.1RT+ Cetuximab72.795% Confidence Interval 51.8 to 86.8percentage of participants
Percentage of Participants With Complete or Partial Response at 4-month Scan Determined by Response Evaluation Criteria in Solid Tumors (RECIST) v. 1.1RT + Durvalumab75.995% Confidence Interval 57.9 to 87.8percentage of participants
Number of Participants by Highest Grade Adverse Event ReportedRT+ Cetuximab< Grade 312Participants
Number of Participants by Highest Grade Adverse Event ReportedRT + Durvalumab< Grade 336Participants
Number of Participants by Highest Grade Adverse Event ReportedRT+ CetuximabGrade 337Participants
Number of Participants by Highest Grade Adverse Event ReportedRT + DurvalumabGrade 357Participants
Number of Participants by Highest Grade Adverse Event ReportedRT+ CetuximabGrade 411Participants
Number of Participants by Highest Grade Adverse Event ReportedRT + DurvalumabGrade 415Participants
Number of Participants by Highest Grade Adverse Event ReportedRT+ CetuximabGrade 51Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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