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Trial · NCT01966471

Results by group551

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

OutcomeGroupCategoryValueSpreadUnits
Invasive Disease-Free Survival (IDFS) in the Node-Positive SubpopulationAnthracycline Followed by Trastuzumab, Pertuzumab, and Taxane94.1095% Confidence Interval 92.46 to 95.73Percent Probability
Invasive Disease-Free Survival (IDFS) in the Node-Positive SubpopulationAnthracycline Followed by Trastuzumab Emtansine and Pertuzumab92.7595% Confidence Interval 90.95 to 94.54Percent Probability
Invasive Disease-Free Survival (IDFS) in the Overall PopulationAnthracycline Followed by Trastuzumab, Pertuzumab, and Taxane94.2295% Confidence Interval 92.68 to 95.76Percent Probability
Invasive Disease-Free Survival (IDFS) in the Overall PopulationAnthracycline Followed by Trastuzumab Emtansine and Pertuzumab93.0695% Confidence Interval 91.40 to 94.73Percent Probability
IDFS Plus Second Primary Non-Breast CancerAnthracycline Followed by Trastuzumab, Pertuzumab, and Taxane93.4395% Confidence Interval 91.79 to 95.06Percent Probability
IDFS Plus Second Primary Non-Breast CancerAnthracycline Followed by Trastuzumab Emtansine and Pertuzumab92.2695% Confidence Interval 90.51 to 94.02Percent Probability
Disease-Free Survival (DFS)Anthracycline Followed by Trastuzumab, Pertuzumab, and Taxane93.3295% Confidence Interval 91.67 to 94.97Percent Probability
Disease-Free Survival (DFS)Anthracycline Followed by Trastuzumab Emtansine and Pertuzumab92.0495% Confidence Interval 90.26 to 93.81Percent Probability
Distant Recurrence-Free Interval (DRFI)Anthracycline Followed by Trastuzumab, Pertuzumab, and Taxane95.2395% Confidence Interval 93.82 to 96.64Percent Probability
Distant Recurrence-Free Interval (DRFI)Anthracycline Followed by Trastuzumab Emtansine and Pertuzumab94.9195% Confidence Interval 93.46 to 96.36Percent Probability
Overall Survival (OS)Anthracycline Followed by Trastuzumab, Pertuzumab, and Taxane96.0395% Confidence Interval 94.72 to 97.34Percent Probability
Overall Survival (OS)Anthracycline Followed by Trastuzumab Emtansine and Pertuzumab94.8695% Confidence Interval 93.40 to 96.32Percent Probability
Percentage of Participants With Adverse EventsAnthracycline Followed by Trastuzumab, Pertuzumab, and Taxane98.5Percentage of participants
Percentage of Participants With Adverse EventsAnthracycline Followed by Trastuzumab Emtansine and Pertuzumab99.1Percentage of participants
Percentage of Participants With Decrease in Left Ventricular Ejection Fraction (LVEF) From Baseline Over TimeAnthracycline Followed by Trastuzumab, Pertuzumab, and TaxaneDecrease from baseline <10 Ejection Fraction (EF) points506Participants
Percentage of Participants With Decrease in Left Ventricular Ejection Fraction (LVEF) From Baseline Over TimeAnthracycline Followed by Trastuzumab Emtansine and PertuzumabDecrease from baseline <10 Ejection Fraction (EF) points522Participants
Percentage of Participants With Decrease in Left Ventricular Ejection Fraction (LVEF) From Baseline Over TimeAnthracycline Followed by Trastuzumab, Pertuzumab, and TaxaneAbsolute value >= 50% and decrease from baseline >= 10 EF points254Participants
Percentage of Participants With Decrease in Left Ventricular Ejection Fraction (LVEF) From Baseline Over TimeAnthracycline Followed by Trastuzumab Emtansine and PertuzumabAbsolute value >= 50% and decrease from baseline >= 10 EF points245Participants
Percentage of Participants With Decrease in Left Ventricular Ejection Fraction (LVEF) From Baseline Over TimeAnthracycline Followed by Trastuzumab, Pertuzumab, and TaxaneAbsolute value < 50% and decrease from baseline >= 10 EF points71Participants
Percentage of Participants With Decrease in Left Ventricular Ejection Fraction (LVEF) From Baseline Over TimeAnthracycline Followed by Trastuzumab Emtansine and PertuzumabAbsolute value < 50% and decrease from baseline >= 10 EF points35Participants

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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