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
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2400
Placebo + Trastuzumab + Chemotherapy
2404
Reported measurements
Baseline: Not anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2286
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
47.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
44.7
Not reported
Not reported
Not reported
Not reported
Baseline: Moderate anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2286
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
49.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
50.1
Not reported
Not reported
Not reported
Not reported
Baseline: Extreme anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2286
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
3.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
5.2
Not reported
Not reported
Not reported
Not reported
Week 13: Not anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2076
Placebo + Trastuzumab + Chemotherapy
2125
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
53.6
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
52.4
Not reported
Not reported
Not reported
Not reported
Week 13: Moderate anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2076
Placebo + Trastuzumab + Chemotherapy
2125
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
43.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
44.0
Not reported
Not reported
Not reported
Not reported
Week 13: Extreme anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2076
Placebo + Trastuzumab + Chemotherapy
2125
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
3.0
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
3.7
Not reported
Not reported
Not reported
Not reported
Week 25: No anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2060
Placebo + Trastuzumab + Chemotherapy
2075
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
55.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
55.5
Not reported
Not reported
Not reported
Not reported
Week 25: Moderate anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2060
Placebo + Trastuzumab + Chemotherapy
2075
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
41.9
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
41.8
Not reported
Not reported
Not reported
Not reported
Week 25: Extreme anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2060
Placebo + Trastuzumab + Chemotherapy
2075
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
2.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
2.7
Not reported
Not reported
Not reported
Not reported
EOT: Not anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2041
Placebo + Trastuzumab + Chemotherapy
2101
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
58.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
58.3
Not reported
Not reported
Not reported
Not reported
EOT: Moderate anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2041
Placebo + Trastuzumab + Chemotherapy
2101
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
38.9
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
39.1
Not reported
Not reported
Not reported
Not reported
EOT: Extreme anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2041
Placebo + Trastuzumab + Chemotherapy
2101
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
2.6
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
2.6
Not reported
Not reported
Not reported
Not reported
FU Month 18: Not anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1916
Placebo + Trastuzumab + Chemotherapy
1915
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
61.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
59.9
Not reported
Not reported
Not reported
Not reported
FU Month 18: Moderate anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1916
Placebo + Trastuzumab + Chemotherapy
1915
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
36.2
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
37.0
Not reported
Not reported
Not reported
Not reported
FU Month 18: Extreme anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1916
Placebo + Trastuzumab + Chemotherapy
1915
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
2.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
3.1
Not reported
Not reported
Not reported
Not reported
FU Month 24: Not anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1860
Placebo + Trastuzumab + Chemotherapy
1872
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
63.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
61.0
Not reported
Not reported
Not reported
Not reported
FU Month 24: Moderate anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1860
Placebo + Trastuzumab + Chemotherapy
1872
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
33.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
36.2
Not reported
Not reported
Not reported
Not reported
FU Month 24: Extreme anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1860
Placebo + Trastuzumab + Chemotherapy
1872
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
2.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
2.8
Not reported
Not reported
Not reported
Not reported
FU Month 36: Not anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1815
Placebo + Trastuzumab + Chemotherapy
1787
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
64.0
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
61.6
Not reported
Not reported
Not reported
Not reported
FU Month 36: Moderate anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1815
Placebo + Trastuzumab + Chemotherapy
1787
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
33.3
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
35.4
Not reported
Not reported
Not reported
Not reported
FU Month 36: Extreme anxious/depress
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1815
Placebo + Trastuzumab + Chemotherapy
1787
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
2.6
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
3.0
Not reported
Not reported
Not reported
Not reported
Complete source fields
classes
categories
measurements
group Id
OG000
value
47.1
group Id
OG001
value
44.7
denoms
counts
group Id
OG000
value
2286
group Id
OG001
value
2310
units
Participants
title
Baseline: Not anxious/depress
categories
measurements
group Id
OG000
value
49.4
group Id
OG001
value
50.1
denoms
counts
group Id
OG000
value
2286
group Id
OG001
value
2310
units
Participants
title
Baseline: Moderate anxious/depress
categories
measurements
group Id
OG000
value
3.5
group Id
OG001
value
5.2
denoms
counts
group Id
OG000
value
2286
group Id
OG001
value
2310
units
Participants
title
Baseline: Extreme anxious/depress
categories
measurements
group Id
OG000
value
53.6
group Id
OG001
value
52.4
denoms
counts
group Id
OG000
value
2076
group Id
OG001
value
2125
units
Participants
title
Week 13: Not anxious/depress
categories
measurements
group Id
OG000
value
43.4
group Id
OG001
value
44.0
denoms
counts
group Id
OG000
value
2076
group Id
OG001
value
2125
units
Participants
title
Week 13: Moderate anxious/depress
categories
measurements
group Id
OG000
value
3.0
group Id
OG001
value
3.7
denoms
counts
group Id
OG000
value
2076
group Id
OG001
value
2125
units
Participants
title
Week 13: Extreme anxious/depress
categories
measurements
group Id
OG000
value
55.5
group Id
OG001
value
55.5
denoms
counts
group Id
OG000
value
2060
group Id
OG001
value
2075
units
Participants
title
Week 25: No anxious/depress
categories
measurements
group Id
OG000
value
41.9
group Id
OG001
value
41.8
denoms
counts
group Id
OG000
value
2060
group Id
OG001
value
2075
units
Participants
title
Week 25: Moderate anxious/depress
categories
measurements
group Id
OG000
value
2.5
group Id
OG001
value
2.7
denoms
counts
group Id
OG000
value
2060
group Id
OG001
value
2075
units
Participants
title
Week 25: Extreme anxious/depress
categories
measurements
group Id
OG000
value
58.5
group Id
OG001
value
58.3
denoms
counts
group Id
OG000
value
2041
group Id
OG001
value
2101
units
Participants
title
EOT: Not anxious/depress
categories
measurements
group Id
OG000
value
38.9
group Id
OG001
value
39.1
denoms
counts
group Id
OG000
value
2041
group Id
OG001
value
2101
units
Participants
title
EOT: Moderate anxious/depress
categories
measurements
group Id
OG000
value
2.6
group Id
OG001
value
2.6
denoms
counts
group Id
OG000
value
2041
group Id
OG001
value
2101
units
Participants
title
EOT: Extreme anxious/depress
denoms
counts
group Id
OG000
value
2400
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
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
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