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NCT01358877 · OUTCOME

Percentage of Participants With Response for European Quality of Life-5 Dimensions-3 Level (EQ-5D-3L) Questionnaire: Mobility Domain

A Study of Pertuzumab in Addition to Chemotherapy and Trastuzumab as Adjuvant Therapy in Participants With Human Epidermal Growth Receptor 2 (HER2)-Positive Primary Breast Cancer · Source last updated 2025-11-28

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
NUMBER
Unit
percentage of participants
Interval / dispersion
Not reported
Time frame
Baseline, Weeks 13, 25; EOT (28 days after the last dose, up to Week 56); FU Months 18, 24, 36

What was measured

EQ-5D-3L is a descriptive system of health-related quality of life states consisting of 5 dimensions/domains (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) and each of which has 3 levels of severity (no problems \[scored as 1\], some or moderate problems \[scored as 2\], and extreme problems \[scored as 3\]). Percentage of participants with each of the following responses in mobility domain was reported: I have no problems in walking about; I have some problems in walking about; and I am confined to bed. Response percentages may not add up to 100% due to data rounding.

Analysis population: ITT population. Number analyzed=participants evaluable for this outcome measure at specified timepoint.

Groups in this outcome

Pertuzumab + Trastuzumab + Chemotherapy

Participants received pertuzumab (840 mg loading dose, then 420 mg) and trastuzumab (8 mg/kg loading dose, then 6 mg/kg) IV Q3W for 1 year (maximum 18 cycles) in combination with 1 of the following IV chemotherapy regimen (anthracycline-based or nonanthracycline-based) per Investigator's choice: 1) 3-4 cycles (Q3W) of 5-fluorouracil 500-600 mg/m\^2 + epirubicin 90-120 mg/m\^2 or doxorubicin 50 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W (100 mg/m\^2 for 3 cycles, 75 mg/m\^2 in first cycle and 100 mg/m\^2 in subsequent cycles, or 75 mg/m\^2 for 4 cycles) or 12 cycles of paclitaxel 80 mg/m\^2 QW; 2) 4 cycles (Q3W) of doxorubicin 60 mg/m\^2 or epirubicin 90-120 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W or 12 cycles of paclitaxel QW (as described in Option 1); 3) 6 cycles (Q3W) of docetaxel 75 mg/m\^2 + carboplatin area under the curve (AUC) 6 (up to 900 mg).

Placebo + Trastuzumab + Chemotherapy

Participants received placebo matched to pertuzumab IV Q3W and trastuzumab (8 mg/kg loading dose, then 6 mg/kg) IV Q3W for 1 year (maximum 18 cycles) in combination with 1 of the following IV chemotherapy regimen (anthracycline-based or nonanthracycline-based) per Investigator's choice: 1) 3-4 cycles (Q3W) of 5-fluorouracil 500-600 mg/m\^2 + epirubicin 90-120 mg/m\^2 or doxorubicin 50 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W (100 mg/m\^2 for 3 cycles, 75 mg/m\^2 in first cycle and 100 mg/m\^2 in subsequent cycles, or 75 mg/m\^2 for 4 cycles) or 12 cycles of paclitaxel 80 mg/m\^2 QW; 2) 4 cycles (Q3W) of doxorubicin 60 mg/m\^2 or epirubicin 90-120 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W or 12 cycles of paclitaxel QW (as described in Option 1); 3) 6 cycles (Q3W) of docetaxel 75 mg/m\^2 + carboplatin AUC 6 (up to 900 mg).

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2400
Placebo + Trastuzumab + Chemotherapy2404

Reported measurements

Baseline: No problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2292
Placebo + Trastuzumab + Chemotherapy2310
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy93.8Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy92.9Not reportedNot reportedNot reportedNot reported
Baseline: Some problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2292
Placebo + Trastuzumab + Chemotherapy2310
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy6.2Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy6.9Not reportedNot reportedNot reportedNot reported
Baseline: Confined to bed

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2292
Placebo + Trastuzumab + Chemotherapy2310
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy0.0Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy0.2Not reportedNot reportedNot reportedNot reported
Week 13: No problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2080
Placebo + Trastuzumab + Chemotherapy2129
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy77.5Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy74.8Not reportedNot reportedNot reportedNot reported
Week 13: Some problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2080
Placebo + Trastuzumab + Chemotherapy2129
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy22.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy24.8Not reportedNot reportedNot reportedNot reported
Week 13: Confined to bed

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2080
Placebo + Trastuzumab + Chemotherapy2129
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy0.4Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy0.4Not reportedNot reportedNot reportedNot reported
Week 25: No problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2062
Placebo + Trastuzumab + Chemotherapy2081
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy83.8Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy82.7Not reportedNot reportedNot reportedNot reported
Week 25: Some problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2062
Placebo + Trastuzumab + Chemotherapy2081
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy16.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy17.2Not reportedNot reportedNot reportedNot reported
Week 25: Confined to bed

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2062
Placebo + Trastuzumab + Chemotherapy2081
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy0.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy0.1Not reportedNot reportedNot reportedNot reported
EOT: No problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2051
Placebo + Trastuzumab + Chemotherapy2106
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy85.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy84.9Not reportedNot reportedNot reportedNot reported
EOT: Some problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2051
Placebo + Trastuzumab + Chemotherapy2106
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy14.8Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy14.9Not reportedNot reportedNot reportedNot reported
EOT: Confined to bed

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2051
Placebo + Trastuzumab + Chemotherapy2106
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy0.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy0.2Not reportedNot reportedNot reportedNot reported
FU Month 18: No problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1920
Placebo + Trastuzumab + Chemotherapy1919
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy88.8Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy87.0Not reportedNot reportedNot reportedNot reported
FU Month 18: Some problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1920
Placebo + Trastuzumab + Chemotherapy1919
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy11.2Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy12.8Not reportedNot reportedNot reportedNot reported
FU Month 18: Confined to bed

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1920
Placebo + Trastuzumab + Chemotherapy1919
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy0.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy0.2Not reportedNot reportedNot reportedNot reported
FU Month 24: No problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1864
Placebo + Trastuzumab + Chemotherapy1877
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy87.8Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy87.7Not reportedNot reportedNot reportedNot reported
FU Month 24: Some problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1864
Placebo + Trastuzumab + Chemotherapy1877
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy12.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy12.1Not reportedNot reportedNot reportedNot reported
FU Month 24: Confined to bed

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1864
Placebo + Trastuzumab + Chemotherapy1877
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy0.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy0.1Not reportedNot reportedNot reportedNot reported
FU Month 36: No problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1822
Placebo + Trastuzumab + Chemotherapy1795
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy88.5Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy87.8Not reportedNot reportedNot reportedNot reported
FU Month 36: Some problems

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1822
Placebo + Trastuzumab + Chemotherapy1795
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy11.5Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy12.1Not reportedNot reportedNot reportedNot reported
FU Month 36: Confined to bed

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1822
Placebo + Trastuzumab + Chemotherapy1795
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy0.0Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy0.1Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        93.8
      2. group Id
        OG001
        value
        92.9
    denoms
    1. counts
      1. group Id
        OG000
        value
        2292
      2. group Id
        OG001
        value
        2310
      units
      Participants
    title
    Baseline: No problems
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        6.2
      2. group Id
        OG001
        value
        6.9
    denoms
    1. counts
      1. group Id
        OG000
        value
        2292
      2. group Id
        OG001
        value
        2310
      units
      Participants
    title
    Baseline: Some problems
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        0.0
      2. group Id
        OG001
        value
        0.2
    denoms
    1. counts
      1. group Id
        OG000
        value
        2292
      2. group Id
        OG001
        value
        2310
      units
      Participants
    title
    Baseline: Confined to bed
  4. categories
    1. measurements
      1. group Id
        OG000
        value
        77.5
      2. group Id
        OG001
        value
        74.8
    denoms
    1. counts
      1. group Id
        OG000
        value
        2080
      2. group Id
        OG001
        value
        2129
      units
      Participants
    title
    Week 13: No problems
  5. categories
    1. measurements
      1. group Id
        OG000
        value
        22.1
      2. group Id
        OG001
        value
        24.8
    denoms
    1. counts
      1. group Id
        OG000
        value
        2080
      2. group Id
        OG001
        value
        2129
      units
      Participants
    title
    Week 13: Some problems
  6. categories
    1. measurements
      1. group Id
        OG000
        value
        0.4
      2. group Id
        OG001
        value
        0.4
    denoms
    1. counts
      1. group Id
        OG000
        value
        2080
      2. group Id
        OG001
        value
        2129
      units
      Participants
    title
    Week 13: Confined to bed
  7. categories
    1. measurements
      1. group Id
        OG000
        value
        83.8
      2. group Id
        OG001
        value
        82.7
    denoms
    1. counts
      1. group Id
        OG000
        value
        2062
      2. group Id
        OG001
        value
        2081
      units
      Participants
    title
    Week 25: No problems
  8. categories
    1. measurements
      1. group Id
        OG000
        value
        16.1
      2. group Id
        OG001
        value
        17.2
    denoms
    1. counts
      1. group Id
        OG000
        value
        2062
      2. group Id
        OG001
        value
        2081
      units
      Participants
    title
    Week 25: Some problems
  9. categories
    1. measurements
      1. group Id
        OG000
        value
        0.1
      2. group Id
        OG001
        value
        0.1
    denoms
    1. counts
      1. group Id
        OG000
        value
        2062
      2. group Id
        OG001
        value
        2081
      units
      Participants
    title
    Week 25: Confined to bed
  10. categories
    1. measurements
      1. group Id
        OG000
        value
        85.1
      2. group Id
        OG001
        value
        84.9
    denoms
    1. counts
      1. group Id
        OG000
        value
        2051
      2. group Id
        OG001
        value
        2106
      units
      Participants
    title
    EOT: No problems
  11. categories
    1. measurements
      1. group Id
        OG000
        value
        14.8
      2. group Id
        OG001
        value
        14.9
    denoms
    1. counts
      1. group Id
        OG000
        value
        2051
      2. group Id
        OG001
        value
        2106
      units
      Participants
    title
    EOT: Some problems
  12. categories
    1. measurements
      1. group Id
        OG000
        value
        0.1
      2. group Id
        OG001
        value
        0.2
    denoms
    1. counts
      1. group Id
        OG000
        value
        2051
      2. group Id
        OG001
        value
        2106
      units
      Participants
    title
    EOT: Confined to bed
denoms
  1. counts
    1. group Id
      OG000
      value
      2400
    2. group Id
      OG001
      value
      2404
    units
    Participants
description
EQ-5D-3L is a descriptive system of health-related quality of life states consisting of 5 dimensions/domains (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) and each of which has 3 levels of severity (no problems \[scored as 1\], some or moderate problems \[scored as 2\], and extreme problems \[scored as 3\]). Percentage of participants with each of the following responses in mobility domain was reported: I have no problems in walking about; I have some problems in walking about; and I am confined to bed. Response percentages may not add up to 100% due to data rounding.
groups
  1. description
    Participants received pertuzumab (840 mg loading dose, then 420 mg) and trastuzumab (8 mg/kg loading dose, then 6 mg/kg) IV Q3W for 1 year (maximum 18 cycles) in combination with 1 of the following IV chemotherapy regimen (anthracycline-based or nonanthracycline-based) per Investigator's choice: 1) 3-4 cycles (Q3W) of 5-fluorouracil 500-600 mg/m\^2 + epirubicin 90-120 mg/m\^2 or doxorubicin 50 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W (100 mg/m\^2 for 3 cycles, 75 mg/m\^2 in first cycle and 100 mg/m\^2 in subsequent cycles, or 75 mg/m\^2 for 4 cycles) or 12 cycles of paclitaxel 80 mg/m\^2 QW; 2) 4 cycles (Q3W) of doxorubicin 60 mg/m\^2 or epirubicin 90-120 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W or 12 cycles of paclitaxel QW (as described in Option 1); 3) 6 cycles (Q3W) of docetaxel 75 mg/m\^2 + carboplatin area under the curve (AUC) 6 (up to 900 mg).
    id
    OG000
    title
    Pertuzumab + Trastuzumab + Chemotherapy
  2. description
    Participants received placebo matched to pertuzumab IV Q3W and trastuzumab (8 mg/kg loading dose, then 6 mg/kg) IV Q3W for 1 year (maximum 18 cycles) in combination with 1 of the following IV chemotherapy regimen (anthracycline-based or nonanthracycline-based) per Investigator's choice: 1) 3-4 cycles (Q3W) of 5-fluorouracil 500-600 mg/m\^2 + epirubicin 90-120 mg/m\^2 or doxorubicin 50 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W (100 mg/m\^2 for 3 cycles, 75 mg/m\^2 in first cycle and 100 mg/m\^2 in subsequent cycles, or 75 mg/m\^2 for 4 cycles) or 12 cycles of paclitaxel 80 mg/m\^2 QW; 2) 4 cycles (Q3W) of doxorubicin 60 mg/m\^2 or epirubicin 90-120 mg/m\^2 + cyclophosphamide 500-600 mg/m\^2 followed by either 3-4 cycles of docetaxel Q3W or 12 cycles of paclitaxel QW (as described in Option 1); 3) 6 cycles (Q3W) of docetaxel 75 mg/m\^2 + carboplatin AUC 6 (up to 900 mg).
    id
    OG001
    title
    Placebo + Trastuzumab + Chemotherapy
param Type
NUMBER
population Description
ITT population. Number analyzed=participants evaluable for this outcome measure at specified timepoint.
reporting Status
POSTED
time Frame
Baseline, Weeks 13, 25; EOT (28 days after the last dose, up to Week 56); FU Months 18, 24, 36
title
Percentage of Participants With Response for European Quality of Life-5 Dimensions-3 Level (EQ-5D-3L) Questionnaire: Mobility Domain
type
SECONDARY
unit Of Measure
percentage of participants

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice