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Trial · NCT01358877

Results by group636

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

OutcomeGroupCategoryValueSpreadUnits
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Excluding SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy6 Years90.5695% Confidence Interval 89.35 to 91.77Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Excluding SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy6 Years87.7695% Confidence Interval 86.40 to 89.13Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Excluding SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy8 Years88.4395% Confidence Interval 87.10 to 89.76Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Excluding SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy8 Years85.7695% Confidence Interval 84.32 to 87.21Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Excluding SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy10 Years87.1795% Confidence Interval 85.77 to 88.57Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Excluding SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy10 Years83.8295% Confidence Interval 82.29 to 85.36Estimate of percentage of participants
Percentage of Participants With IDFS Event (Including SPNBC), as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy7.9percentage of participants
Percentage of Participants With IDFS Event (Including SPNBC), as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy9.6percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 3 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy93.5095% Confidence Interval 92.49 to 94.51Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 3 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy92.5195% Confidence Interval 91.43 to 93.58Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy6 Years89.3195% Confidence Interval 88.03 to 90.59Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy6 Years86.4295% Confidence Interval 85.00 to 87.44Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy8 Years87.0895% Confidence Interval 85.69 to 88.48Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy8 Years83.8295% Confidence Interval 82.29 to 85.34Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy10 Years85.2395% Confidence Interval 83.74 to 86.71Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were IDFS Event-Free (Including SPNBC) at 6, 8, and 10 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy10 Years81.3195% Confidence Interval 79.69 to 82.93Estimate of percentage of participants
Percentage of Participants With Disease-Free Survival (DFS) Event, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy8.0percentage of participants
Percentage of Participants With Disease-Free Survival (DFS) Event, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy9.8percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were DFS Event-Free at 3 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPertuzumab + Trastuzumab + Chemotherapy93.4295% Confidence Interval 92.40 to 94.43Estimate of percentage of participants
Kaplan-Meier Estimate of the Percentage of Participants Who Were DFS Event-Free at 3 Years, as Assessed Using Radiologic, Histologic Examinations or Laboratory FindingsPlacebo + Trastuzumab + Chemotherapy92.2995% Confidence Interval 91.21 to 93.38Estimate of percentage 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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