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Trial · NCT00769379

Results by group14

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

OutcomeGroupCategoryValueSpreadUnits
Ipsilateral Invasive Breast Cancer, Ipsilateral Skin Cancer Recurrence, or Ipsilateral DCIS-Free SurvivalArm I (Standard WBI)95.195% Confidence Interval 93.8 to 96.5percentage of patients event free
Ipsilateral Invasive Breast Cancer, Ipsilateral Skin Cancer Recurrence, or Ipsilateral DCIS-Free SurvivalArm II (WBI, Trastuzumab)96.195% Confidence Interval 94.9 to 97.3percentage of patients event free
Invasive or DCIS Disease-free SurvivalArm I (Standard WBI)88.495% Confidence Interval 86.3 to 90.4percentage of patients event free
Invasive or DCIS Disease-free SurvivalArm II (WBI, Trastuzumab)90.695% Confidence Interval 88.8 to 92.5percentage of patients event free
Invasive or DCIS Recurrence-free IntervalArm I (Standard WBI)94.495% Confidence Interval 92.9 to 95.8percentage of patients event free
Invasive or DCIS Recurrence-free IntervalArm II (WBI, Trastuzumab)95.895% Confidence Interval 94.5 to 97.1percentage of patients event free
Invasive Regional or Distant-Free RecurrenceArm I (Standard WBI)99.995% Confidence Interval 99.7 to 100.0percentage of patients event free
Invasive Regional or Distant-Free RecurrenceArm II (WBI, Trastuzumab)99.995% Confidence Interval 99.7 to 100.0percentage of patients event free
Contralateral Breast Cancer (Invasive or DCIS) - Free SurvivalArm I (Standard WBI)97.995% Confidence Interval 97.0 to 98.8percentage of patients event free
Contralateral Breast Cancer (Invasive or DCIS) - Free SurvivalArm II (WBI, Trastuzumab)98.495% Confidence Interval 97.6 to 99.2percentage of patients event free
Overall SurvivalArm I (Standard WBI)98.995% Confidence Interval 98.2 to 99.5percentage of patients surviving
Overall SurvivalArm II (WBI, Trastuzumab)99.095% Confidence Interval 98.3 to 99.6percentage of patients surviving
Incidence of Post-treatment Amenorrhea in Women Who Were Premenopausal at the Time of Study Entry Premenopausal at the Time of Study EntryArm I (Standard WBI)63percentage of participants
Incidence of Post-treatment Amenorrhea in Women Who Were Premenopausal at the Time of Study Entry Premenopausal at the Time of Study EntryArm II (WBI, Trastuzumab)72percentage of participants

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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