Percentage of Participants With Response for EQ-5D-3L Questionnaire: Self-Care 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 self-care domain was reported: I have no problems with self-care; I have some problems washing or dressing myself; and I am unable to wash or dress myself. 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
2289
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
89.7
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
90.7
Not reported
Not reported
Not reported
Not reported
Baseline: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2289
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
10.0
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
9.1
Not reported
Not reported
Not reported
Not reported
Baseline: Unable
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2289
Placebo + Trastuzumab + Chemotherapy
2310
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.3
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
2079
Placebo + Trastuzumab + Chemotherapy
2127
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
94.3
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
93.2
Not reported
Not reported
Not reported
Not reported
Week 13: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2079
Placebo + Trastuzumab + Chemotherapy
2127
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
5.3
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
6.4
Not reported
Not reported
Not reported
Not reported
Week 13: Unable
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2079
Placebo + Trastuzumab + Chemotherapy
2127
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
2057
Placebo + Trastuzumab + Chemotherapy
2077
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
95.5
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
95.0
Not reported
Not reported
Not reported
Not reported
Week 25: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2057
Placebo + Trastuzumab + Chemotherapy
2077
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
4.3
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
4.7
Not reported
Not reported
Not reported
Not reported
Week 25: Unable
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
2057
Placebo + Trastuzumab + Chemotherapy
2077
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
0.3
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
95.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
95.8
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
4.4
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
4.0
Not reported
Not reported
Not reported
Not reported
EOT: Unable
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
0.2
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
1917
Placebo + Trastuzumab + Chemotherapy
1921
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
97.2
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
96.0
Not reported
Not reported
Not reported
Not reported
FU Month 18: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1917
Placebo + Trastuzumab + Chemotherapy
1921
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
3.6
Not reported
Not reported
Not reported
Not reported
FU Month 18: Unable
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1917
Placebo + Trastuzumab + Chemotherapy
1921
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.2
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.3
Not reported
Not reported
Not reported
Not reported
FU Month 24: No problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1861
Placebo + Trastuzumab + Chemotherapy
1877
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
96.9
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
96.3
Not reported
Not reported
Not reported
Not reported
FU Month 24: Some problems
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1861
Placebo + Trastuzumab + Chemotherapy
1877
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
2.8
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
3.5
Not reported
Not reported
Not reported
Not reported
FU Month 24: Unable
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1861
Placebo + Trastuzumab + Chemotherapy
1877
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.3
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.3
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
1794
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
97.3
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
96.5
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
1794
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
3.2
Not reported
Not reported
Not reported
Not reported
FU Month 36: Unable
Analysis denominator · Participants
Group
Source count
Pertuzumab + Trastuzumab + Chemotherapy
1822
Placebo + Trastuzumab + Chemotherapy
1794
Values in percentage of participants · Interval/dispersion: Not reported
Group
Value
Spread
Lower
Upper
Comment
Pertuzumab + Trastuzumab + Chemotherapy
0.2
Not reported
Not reported
Not reported
Not reported
Placebo + Trastuzumab + Chemotherapy
0.3
Not reported
Not reported
Not reported
Not reported
Complete source fields
classes
categories
measurements
group Id
OG000
value
89.7
group Id
OG001
value
90.7
denoms
counts
group Id
OG000
value
2289
group Id
OG001
value
2310
units
Participants
title
Baseline: No problems
categories
measurements
group Id
OG000
value
10.0
group Id
OG001
value
9.1
denoms
counts
group Id
OG000
value
2289
group Id
OG001
value
2310
units
Participants
title
Baseline: Some problems
categories
measurements
group Id
OG000
value
0.3
group Id
OG001
value
0.2
denoms
counts
group Id
OG000
value
2289
group Id
OG001
value
2310
units
Participants
title
Baseline: Unable
categories
measurements
group Id
OG000
value
94.3
group Id
OG001
value
93.2
denoms
counts
group Id
OG000
value
2079
group Id
OG001
value
2127
units
Participants
title
Week 13: No problems
categories
measurements
group Id
OG000
value
5.3
group Id
OG001
value
6.4
denoms
counts
group Id
OG000
value
2079
group Id
OG001
value
2127
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
2079
group Id
OG001
value
2127
units
Participants
title
Week 13: Unable
categories
measurements
group Id
OG000
value
95.5
group Id
OG001
value
95.0
denoms
counts
group Id
OG000
value
2057
group Id
OG001
value
2077
units
Participants
title
Week 25: No problems
categories
measurements
group Id
OG000
value
4.3
group Id
OG001
value
4.7
denoms
counts
group Id
OG000
value
2057
group Id
OG001
value
2077
units
Participants
title
Week 25: Some problems
categories
measurements
group Id
OG000
value
0.1
group Id
OG001
value
0.3
denoms
counts
group Id
OG000
value
2057
group Id
OG001
value
2077
units
Participants
title
Week 25: Unable
categories
measurements
group Id
OG000
value
95.4
group Id
OG001
value
95.8
denoms
counts
group Id
OG000
value
2051
group Id
OG001
value
2106
units
Participants
title
EOT: No problems
categories
measurements
group Id
OG000
value
4.4
group Id
OG001
value
4.0
denoms
counts
group Id
OG000
value
2051
group Id
OG001
value
2106
units
Participants
title
EOT: Some problems
categories
measurements
group Id
OG000
value
0.2
group Id
OG001
value
0.2
denoms
counts
group Id
OG000
value
2051
group Id
OG001
value
2106
units
Participants
title
EOT: Unable
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 self-care domain was reported: I have no problems with self-care; I have some problems washing or dressing myself; and I am unable to wash or dress myself. 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: Self-Care Domain