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
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2400
Placebo + Trastuzumab + Chemotherapy
2404
Reported measurements
Baseline: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2292
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
93.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
92.9
Not reported
Not reported
Not reported
Not reported
Baseline: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2292
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
6.2
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
6.9
Not reported
Not reported
Not reported
Not reported
Baseline: Confined to bed
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2292
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.0
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.2
Not reported
Not reported
Not reported
Not reported
Week 13: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2080
Placebo + Trastuzumab + Chemotherapy
2129
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
77.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
74.8
Not reported
Not reported
Not reported
Not reported
Week 13: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2080
Placebo + Trastuzumab + Chemotherapy
2129
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
22.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
24.8
Not reported
Not reported
Not reported
Not reported
Week 13: Confined to bed
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2080
Placebo + Trastuzumab + Chemotherapy
2129
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.4
Not reported
Not reported
Not reported
Not reported
Week 25: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2062
Placebo + Trastuzumab + Chemotherapy
2081
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
83.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
82.7
Not reported
Not reported
Not reported
Not reported
Week 25: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2062
Placebo + Trastuzumab + Chemotherapy
2081
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
16.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
17.2
Not reported
Not reported
Not reported
Not reported
Week 25: Confined to bed
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2062
Placebo + Trastuzumab + Chemotherapy
2081
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.1
Not reported
Not reported
Not reported
Not reported
EOT: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2051
Placebo + Trastuzumab + Chemotherapy
2106
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
85.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
84.9
Not reported
Not reported
Not reported
Not reported
EOT: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2051
Placebo + Trastuzumab + Chemotherapy
2106
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
14.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
14.9
Not reported
Not reported
Not reported
Not reported
EOT: Confined to bed
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2051
Placebo + Trastuzumab + Chemotherapy
2106
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.2
Not reported
Not reported
Not reported
Not reported
FU Month 18: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1920
Placebo + Trastuzumab + Chemotherapy
1919
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
88.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
87.0
Not reported
Not reported
Not reported
Not reported
FU Month 18: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1920
Placebo + Trastuzumab + Chemotherapy
1919
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
11.2
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
12.8
Not reported
Not reported
Not reported
Not reported
FU Month 18: Confined to bed
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1920
Placebo + Trastuzumab + Chemotherapy
1919
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.2
Not reported
Not reported
Not reported
Not reported
FU Month 24: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1864
Placebo + Trastuzumab + Chemotherapy
1877
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
87.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
87.7
Not reported
Not reported
Not reported
Not reported
FU Month 24: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1864
Placebo + Trastuzumab + Chemotherapy
1877
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
12.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
12.1
Not reported
Not reported
Not reported
Not reported
FU Month 24: Confined to bed
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1864
Placebo + Trastuzumab + Chemotherapy
1877
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.1
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.1
Not reported
Not reported
Not reported
Not reported
FU Month 36: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1822
Placebo + Trastuzumab + Chemotherapy
1795
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
88.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
87.8
Not reported
Not reported
Not reported
Not reported
FU Month 36: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1822
Placebo + Trastuzumab + Chemotherapy
1795
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
11.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
12.1
Not reported
Not reported
Not reported
Not reported
FU Month 36: Confined to bed
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1822
Placebo + Trastuzumab + Chemotherapy
1795
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.0
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.1
Not reported
Not reported
Not reported
Not reported
Complete source fields
classes
categories
measurements
group Id
OG000
value
93.8
group Id
OG001
value
92.9
denoms
counts
group Id
OG000
value
2292
group Id
OG001
value
2310
units
Participants
title
Baseline: No problems
categories
measurements
group Id
OG000
value
6.2
group Id
OG001
value
6.9
denoms
counts
group Id
OG000
value
2292
group Id
OG001
value
2310
units
Participants
title
Baseline: Some problems
categories
measurements
group Id
OG000
value
0.0
group Id
OG001
value
0.2
denoms
counts
group Id
OG000
value
2292
group Id
OG001
value
2310
units
Participants
title
Baseline: Confined to bed
categories
measurements
group Id
OG000
value
77.5
group Id
OG001
value
74.8
denoms
counts
group Id
OG000
value
2080
group Id
OG001
value
2129
units
Participants
title
Week 13: No problems
categories
measurements
group Id
OG000
value
22.1
group Id
OG001
value
24.8
denoms
counts
group Id
OG000
value
2080
group Id
OG001
value
2129
units
Participants
title
Week 13: Some problems
categories
measurements
group Id
OG000
value
0.4
group Id
OG001
value
0.4
denoms
counts
group Id
OG000
value
2080
group Id
OG001
value
2129
units
Participants
title
Week 13: Confined to bed
categories
measurements
group Id
OG000
value
83.8
group Id
OG001
value
82.7
denoms
counts
group Id
OG000
value
2062
group Id
OG001
value
2081
units
Participants
title
Week 25: No problems
categories
measurements
group Id
OG000
value
16.1
group Id
OG001
value
17.2
denoms
counts
group Id
OG000
value
2062
group Id
OG001
value
2081
units
Participants
title
Week 25: Some problems
categories
measurements
group Id
OG000
value
0.1
group Id
OG001
value
0.1
denoms
counts
group Id
OG000
value
2062
group Id
OG001
value
2081
units
Participants
title
Week 25: Confined to bed
categories
measurements
group Id
OG000
value
85.1
group Id
OG001
value
84.9
denoms
counts
group Id
OG000
value
2051
group Id
OG001
value
2106
units
Participants
title
EOT: No problems
categories
measurements
group Id
OG000
value
14.8
group Id
OG001
value
14.9
denoms
counts
group Id
OG000
value
2051
group Id
OG001
value
2106
units
Participants
title
EOT: Some problems
categories
measurements
group Id
OG000
value
0.1
group Id
OG001
value
0.2
denoms
counts
group Id
OG000
value
2051
group Id
OG001
value
2106
units
Participants
title
EOT: Confined to bed
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 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
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 European Quality of Life-5 Dimensions-3 Level (EQ-5D-3L) Questionnaire: Mobility Domain