NCT02580058 · OUTCOME
Change From Baseline in Vital Signs - Blood Pressure
A Study Of Avelumab Alone Or In Combination With Pegylated Liposomal Doxorubicin Versus Pegylated Liposomal Doxorubicin Alone In Patients With Platinum Resistant/Refractory Ovarian Cancer (JAVELIN Ovarian 200) · Source last updated 2023-07-10
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEAN
- Unit
- mm Hg
- Interval / dispersion
- Standard Deviation
- Time frame
- From screening to the end of treatment/withdrawal visit, up to 2.7 years, based on cutoff date: 19 September 2018.
What was measured
Vital signs included blood pressure and pulse rate. Changes from baseline in sitting diastolic blood pressure (DBP) and systolic blood pressure (SBP) were summarized.
Analysis population: 'Number of Participants Analyzed' is based on the safety analysis set, which included all participants who received at least 1 dose of study treatment. 'Number Analyzed' included the number of participants in the safety analysis set with at least a baseline and post-baseline assessment at the visit.
Groups in this outcome
Avelumab
Avelumab 10 milligram (mg)/kilogram (kg) given as a 1-hour intravenous (IV) infusion every 2 weeks (Q2W) in 4-week cycles.
Avelumab + PLD
Avelumab 10 mg/kg given as a 1-hour IV Q2W in 4-week cycles + pegylated liposomal doxorubicin (PLD) 40 mg/square meter given as a 1-hour IV infusion every 4 weeks (Q4W) in 4-week cycles.
Pegylated Liposomal Doxorubicin (PLD)
PLD 40 mg/square meter given as a 1-hour IV infusion Q4W in 4-week cycles.
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 |
|---|
| Avelumab | 187 |
|---|
| Avelumab + PLD | 182 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 177 |
|---|
Reported measurements
DBP Cycle 1 Day 15
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 180 |
|---|
| Avelumab + PLD | 170 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 142 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | 0.1 | 9.79 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.2 | 9.12 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 0.7 | 8.89 | Not reported | Not reported | Not reported |
|---|
DBP Cycle 2 Day 1
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 164 |
|---|
| Avelumab + PLD | 168 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 156 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -1.1 | 9.61 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.8 | 8.01 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -0.1 | 9.34 | Not reported | Not reported | Not reported |
|---|
DBP Cycle 2 Day 15
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 138 |
|---|
| Avelumab + PLD | 157 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 124 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | 0.1 | 10.05 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.8 | 9.19 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -0.1 | 8.83 | Not reported | Not reported | Not reported |
|---|
DBP Cycle 3 Day 1
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 104 |
|---|
| Avelumab + PLD | 141 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 106 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | 0 | 10.81 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.7 | 8.95 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -0.2 | 8.96 | Not reported | Not reported | Not reported |
|---|
DBP Cycle 3 Day 15
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 95 |
|---|
| Avelumab + PLD | 128 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 84 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -0.6 | 9.25 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.3 | 8.56 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -0.5 | 8.67 | Not reported | Not reported | Not reported |
|---|
DBP End of Treatment
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 146 |
|---|
| Avelumab + PLD | 138 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 136 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | 1.1 | 10.87 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -0.3 | 11.08 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 0.8 | 10.40 | Not reported | Not reported | Not reported |
|---|
SBP Cycle 1 Day 15
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 180 |
|---|
| Avelumab + PLD | 170 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 142 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -0.9 | 14.35 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.3 | 13.12 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -1.0 | 13.94 | Not reported | Not reported | Not reported |
|---|
SBP Cycle 2 Day 1
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 164 |
|---|
| Avelumab + PLD | 168 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 156 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -2.2 | 14.44 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -3.4 | 13.70 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -2.8 | 13.39 | Not reported | Not reported | Not reported |
|---|
SBP Cycle 2 Day 15
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 138 |
|---|
| Avelumab + PLD | 157 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 124 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -0.6 | 14.11 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -3.7 | 14.78 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -1.8 | 14.98 | Not reported | Not reported | Not reported |
|---|
SBP Cycle 3 Day 1
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 104 |
|---|
| Avelumab + PLD | 141 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 106 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -0.2 | 15.59 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.7 | 14.36 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -1.5 | 14.14 | Not reported | Not reported | Not reported |
|---|
SBP Cycle 3 Day 15
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 95 |
|---|
| Avelumab + PLD | 128 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 84 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -0.2 | 13.78 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -2.1 | 15.30 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -2.2 | 13.96 | Not reported | Not reported | Not reported |
|---|
SBP End of Treatment
Analysis denominator · Participants
| Group | Source count |
|---|
| Avelumab | 146 |
|---|
| Avelumab + PLD | 138 |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | 136 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Avelumab | -0.9 | 17.21 | Not reported | Not reported | Not reported |
|---|
| Avelumab + PLD | -1.0 | 16.83 | Not reported | Not reported | Not reported |
|---|
| Pegylated Liposomal Doxorubicin (PLD) | -3.2 | 15.92 | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 9.79
- value
- 0.1
- group Id
- OG001
- spread
- 9.12
- value
- -2.2
- group Id
- OG002
- spread
- 8.89
- value
- 0.7
- denoms
- counts
- group Id
- OG000
- value
- 180
- group Id
- OG001
- value
- 170
- group Id
- OG002
- value
- 142
- units
- Participants
- title
- DBP Cycle 1 Day 15
- categories
- measurements
- group Id
- OG000
- spread
- 9.61
- value
- -1.1
- group Id
- OG001
- spread
- 8.01
- value
- -2.8
- group Id
- OG002
- spread
- 9.34
- value
- -0.1
- denoms
- counts
- group Id
- OG000
- value
- 164
- group Id
- OG001
- value
- 168
- group Id
- OG002
- value
- 156
- units
- Participants
- title
- DBP Cycle 2 Day 1
- categories
- measurements
- group Id
- OG000
- spread
- 10.05
- value
- 0.1
- group Id
- OG001
- spread
- 9.19
- value
- -2.8
- group Id
- OG002
- spread
- 8.83
- value
- -0.1
- denoms
- counts
- group Id
- OG000
- value
- 138
- group Id
- OG001
- value
- 157
- group Id
- OG002
- value
- 124
- units
- Participants
- title
- DBP Cycle 2 Day 15
- categories
- measurements
- group Id
- OG000
- spread
- 10.81
- value
- 0
- group Id
- OG001
- spread
- 8.95
- value
- -2.7
- group Id
- OG002
- spread
- 8.96
- value
- -0.2
- denoms
- counts
- group Id
- OG000
- value
- 104
- group Id
- OG001
- value
- 141
- group Id
- OG002
- value
- 106
- units
- Participants
- title
- DBP Cycle 3 Day 1
- categories
- measurements
- group Id
- OG000
- spread
- 9.25
- value
- -0.6
- group Id
- OG001
- spread
- 8.56
- value
- -2.3
- group Id
- OG002
- spread
- 8.67
- value
- -0.5
- denoms
- counts
- group Id
- OG000
- value
- 95
- group Id
- OG001
- value
- 128
- group Id
- OG002
- value
- 84
- units
- Participants
- title
- DBP Cycle 3 Day 15
- categories
- measurements
- group Id
- OG000
- spread
- 10.87
- value
- 1.1
- group Id
- OG001
- spread
- 11.08
- value
- -0.3
- group Id
- OG002
- spread
- 10.40
- value
- 0.8
- denoms
- counts
- group Id
- OG000
- value
- 146
- group Id
- OG001
- value
- 138
- group Id
- OG002
- value
- 136
- units
- Participants
- title
- DBP End of Treatment
- categories
- measurements
- group Id
- OG000
- spread
- 14.35
- value
- -0.9
- group Id
- OG001
- spread
- 13.12
- value
- -2.3
- group Id
- OG002
- spread
- 13.94
- value
- -1.0
- denoms
- counts
- group Id
- OG000
- value
- 180
- group Id
- OG001
- value
- 170
- group Id
- OG002
- value
- 142
- units
- Participants
- title
- SBP Cycle 1 Day 15
- categories
- measurements
- group Id
- OG000
- spread
- 14.44
- value
- -2.2
- group Id
- OG001
- spread
- 13.70
- value
- -3.4
- group Id
- OG002
- spread
- 13.39
- value
- -2.8
- denoms
- counts
- group Id
- OG000
- value
- 164
- group Id
- OG001
- value
- 168
- group Id
- OG002
- value
- 156
- units
- Participants
- title
- SBP Cycle 2 Day 1
- categories
- measurements
- group Id
- OG000
- spread
- 14.11
- value
- -0.6
- group Id
- OG001
- spread
- 14.78
- value
- -3.7
- group Id
- OG002
- spread
- 14.98
- value
- -1.8
- denoms
- counts
- group Id
- OG000
- value
- 138
- group Id
- OG001
- value
- 157
- group Id
- OG002
- value
- 124
- units
- Participants
- title
- SBP Cycle 2 Day 15
- categories
- measurements
- group Id
- OG000
- spread
- 15.59
- value
- -0.2
- group Id
- OG001
- spread
- 14.36
- value
- -2.7
- group Id
- OG002
- spread
- 14.14
- value
- -1.5
- denoms
- counts
- group Id
- OG000
- value
- 104
- group Id
- OG001
- value
- 141
- group Id
- OG002
- value
- 106
- units
- Participants
- title
- SBP Cycle 3 Day 1
- categories
- measurements
- group Id
- OG000
- spread
- 13.78
- value
- -0.2
- group Id
- OG001
- spread
- 15.30
- value
- -2.1
- group Id
- OG002
- spread
- 13.96
- value
- -2.2
- denoms
- counts
- group Id
- OG000
- value
- 95
- group Id
- OG001
- value
- 128
- group Id
- OG002
- value
- 84
- units
- Participants
- title
- SBP Cycle 3 Day 15
- categories
- measurements
- group Id
- OG000
- spread
- 17.21
- value
- -0.9
- group Id
- OG001
- spread
- 16.83
- value
- -1.0
- group Id
- OG002
- spread
- 15.92
- value
- -3.2
- denoms
- counts
- group Id
- OG000
- value
- 146
- group Id
- OG001
- value
- 138
- group Id
- OG002
- value
- 136
- units
- Participants
- title
- SBP End of Treatment
- denoms
- counts
- group Id
- OG000
- value
- 187
- group Id
- OG001
- value
- 182
- group Id
- OG002
- value
- 177
- units
- Participants
- description
- Vital signs included blood pressure and pulse rate. Changes from baseline in sitting diastolic blood pressure (DBP) and systolic blood pressure (SBP) were summarized.
- dispersion Type
- Standard Deviation
- groups
- description
- Avelumab 10 milligram (mg)/kilogram (kg) given as a 1-hour intravenous (IV) infusion every 2 weeks (Q2W) in 4-week cycles.
- id
- OG000
- title
- Avelumab
- description
- Avelumab 10 mg/kg given as a 1-hour IV Q2W in 4-week cycles + pegylated liposomal doxorubicin (PLD) 40 mg/square meter given as a 1-hour IV infusion every 4 weeks (Q4W) in 4-week cycles.
- id
- OG001
- title
- Avelumab + PLD
- description
- PLD 40 mg/square meter given as a 1-hour IV infusion Q4W in 4-week cycles.
- id
- OG002
- title
- Pegylated Liposomal Doxorubicin (PLD)
- param Type
- MEAN
- population Description
- 'Number of Participants Analyzed' is based on the safety analysis set, which included all participants who received at least 1 dose of study treatment. 'Number Analyzed' included the number of participants in the safety analysis set with at least a baseline and post-baseline assessment at the visit.
- reporting Status
- POSTED
- time Frame
- From screening to the end of treatment/withdrawal visit, up to 2.7 years, based on cutoff date: 19 September 2018.
- title
- Change From Baseline in Vital Signs - Blood Pressure
- type
- SECONDARY
- unit Of Measure
- mm Hg
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Preserved source evidence · Not medical advice