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NCT01358877 · OUTCOME

Percentage of Participants With Response for EQ-5D-3L Questionnaire: Anxiety/Depression 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 anxiety/depression domain was reported: I am not anxious or depressed; I am moderately anxious or depressed; and I am extremely anxious or depressed. 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: Not anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2286
Placebo + Trastuzumab + Chemotherapy2310
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy47.1Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy44.7Not reportedNot reportedNot reportedNot reported
Baseline: Moderate anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2286
Placebo + Trastuzumab + Chemotherapy2310
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy49.4Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy50.1Not reportedNot reportedNot reportedNot reported
Baseline: Extreme anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2286
Placebo + Trastuzumab + Chemotherapy2310
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy3.5Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy5.2Not reportedNot reportedNot reportedNot reported
Week 13: Not anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2076
Placebo + Trastuzumab + Chemotherapy2125
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy53.6Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy52.4Not reportedNot reportedNot reportedNot reported
Week 13: Moderate anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2076
Placebo + Trastuzumab + Chemotherapy2125
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy43.4Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy44.0Not reportedNot reportedNot reportedNot reported
Week 13: Extreme anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2076
Placebo + Trastuzumab + Chemotherapy2125
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy3.0Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy3.7Not reportedNot reportedNot reportedNot reported
Week 25: No anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2060
Placebo + Trastuzumab + Chemotherapy2075
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy55.5Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy55.5Not reportedNot reportedNot reportedNot reported
Week 25: Moderate anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2060
Placebo + Trastuzumab + Chemotherapy2075
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy41.9Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy41.8Not reportedNot reportedNot reportedNot reported
Week 25: Extreme anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2060
Placebo + Trastuzumab + Chemotherapy2075
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy2.5Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy2.7Not reportedNot reportedNot reportedNot reported
EOT: Not anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2041
Placebo + Trastuzumab + Chemotherapy2101
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy58.5Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy58.3Not reportedNot reportedNot reportedNot reported
EOT: Moderate anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2041
Placebo + Trastuzumab + Chemotherapy2101
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy38.9Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy39.1Not reportedNot reportedNot reportedNot reported
EOT: Extreme anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy2041
Placebo + Trastuzumab + Chemotherapy2101
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy2.6Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy2.6Not reportedNot reportedNot reportedNot reported
FU Month 18: Not anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1916
Placebo + Trastuzumab + Chemotherapy1915
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy61.4Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy59.9Not reportedNot reportedNot reportedNot reported
FU Month 18: Moderate anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1916
Placebo + Trastuzumab + Chemotherapy1915
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy36.2Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy37.0Not reportedNot reportedNot reportedNot reported
FU Month 18: Extreme anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1916
Placebo + Trastuzumab + Chemotherapy1915
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy2.4Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy3.1Not reportedNot reportedNot reportedNot reported
FU Month 24: Not anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1860
Placebo + Trastuzumab + Chemotherapy1872
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy63.8Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy61.0Not reportedNot reportedNot reportedNot reported
FU Month 24: Moderate anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1860
Placebo + Trastuzumab + Chemotherapy1872
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy33.8Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy36.2Not reportedNot reportedNot reportedNot reported
FU Month 24: Extreme anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1860
Placebo + Trastuzumab + Chemotherapy1872
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy2.4Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy2.8Not reportedNot reportedNot reportedNot reported
FU Month 36: Not anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1815
Placebo + Trastuzumab + Chemotherapy1787
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy64.0Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy61.6Not reportedNot reportedNot reportedNot reported
FU Month 36: Moderate anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1815
Placebo + Trastuzumab + Chemotherapy1787
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy33.3Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy35.4Not reportedNot reportedNot reportedNot reported
FU Month 36: Extreme anxious/depress

Analysis denominator · Participants

GroupSource count
Pertuzumab + Trastuzumab + Chemotherapy1815
Placebo + Trastuzumab + Chemotherapy1787
Values in percentage of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pertuzumab + Trastuzumab + Chemotherapy2.6Not reportedNot reportedNot reportedNot reported
Placebo + Trastuzumab + Chemotherapy3.0Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        47.1
      2. group Id
        OG001
        value
        44.7
    denoms
    1. counts
      1. group Id
        OG000
        value
        2286
      2. group Id
        OG001
        value
        2310
      units
      Participants
    title
    Baseline: Not anxious/depress
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        49.4
      2. group Id
        OG001
        value
        50.1
    denoms
    1. counts
      1. group Id
        OG000
        value
        2286
      2. group Id
        OG001
        value
        2310
      units
      Participants
    title
    Baseline: Moderate anxious/depress
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        3.5
      2. group Id
        OG001
        value
        5.2
    denoms
    1. counts
      1. group Id
        OG000
        value
        2286
      2. group Id
        OG001
        value
        2310
      units
      Participants
    title
    Baseline: Extreme anxious/depress
  4. categories
    1. measurements
      1. group Id
        OG000
        value
        53.6
      2. group Id
        OG001
        value
        52.4
    denoms
    1. counts
      1. group Id
        OG000
        value
        2076
      2. group Id
        OG001
        value
        2125
      units
      Participants
    title
    Week 13: Not anxious/depress
  5. categories
    1. measurements
      1. group Id
        OG000
        value
        43.4
      2. group Id
        OG001
        value
        44.0
    denoms
    1. counts
      1. group Id
        OG000
        value
        2076
      2. group Id
        OG001
        value
        2125
      units
      Participants
    title
    Week 13: Moderate anxious/depress
  6. categories
    1. measurements
      1. group Id
        OG000
        value
        3.0
      2. group Id
        OG001
        value
        3.7
    denoms
    1. counts
      1. group Id
        OG000
        value
        2076
      2. group Id
        OG001
        value
        2125
      units
      Participants
    title
    Week 13: Extreme anxious/depress
  7. categories
    1. measurements
      1. group Id
        OG000
        value
        55.5
      2. group Id
        OG001
        value
        55.5
    denoms
    1. counts
      1. group Id
        OG000
        value
        2060
      2. group Id
        OG001
        value
        2075
      units
      Participants
    title
    Week 25: No anxious/depress
  8. categories
    1. measurements
      1. group Id
        OG000
        value
        41.9
      2. group Id
        OG001
        value
        41.8
    denoms
    1. counts
      1. group Id
        OG000
        value
        2060
      2. group Id
        OG001
        value
        2075
      units
      Participants
    title
    Week 25: Moderate anxious/depress
  9. categories
    1. measurements
      1. group Id
        OG000
        value
        2.5
      2. group Id
        OG001
        value
        2.7
    denoms
    1. counts
      1. group Id
        OG000
        value
        2060
      2. group Id
        OG001
        value
        2075
      units
      Participants
    title
    Week 25: Extreme anxious/depress
  10. categories
    1. measurements
      1. group Id
        OG000
        value
        58.5
      2. group Id
        OG001
        value
        58.3
    denoms
    1. counts
      1. group Id
        OG000
        value
        2041
      2. group Id
        OG001
        value
        2101
      units
      Participants
    title
    EOT: Not anxious/depress
  11. categories
    1. measurements
      1. group Id
        OG000
        value
        38.9
      2. group Id
        OG001
        value
        39.1
    denoms
    1. counts
      1. group Id
        OG000
        value
        2041
      2. group Id
        OG001
        value
        2101
      units
      Participants
    title
    EOT: Moderate anxious/depress
  12. categories
    1. measurements
      1. group Id
        OG000
        value
        2.6
      2. group Id
        OG001
        value
        2.6
    denoms
    1. counts
      1. group Id
        OG000
        value
        2041
      2. group Id
        OG001
        value
        2101
      units
      Participants
    title
    EOT: Extreme anxious/depress
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 anxiety/depression domain was reported: I am not anxious or depressed; I am moderately anxious or depressed; and I am extremely anxious or depressed. 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 EQ-5D-3L Questionnaire: Anxiety/Depression Domain
type
SECONDARY
unit Of Measure
percentage of participants

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Preserved source evidence · Not medical advice