NCT04266301 · OUTCOME
Key Secondary Endpoint 5: Percentage of Participants With at Least 10 Point Confirmed Improvement From Baseline in Emotional Functioning Using EORTC-QLQ-C30
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
- 95% Confidence Interval
- Time frame
- up to approx. 52 months
What was measured
EORTC-QLQ-C30 is a 30-item questionnaire developed to assess the quality of life of cancer participants. Participants' responses to 4 questions about their emotional functioning (Items 21-24) are scored on a 4-point scale (1=Not at All to 4=Very Much). Using linear transformation, raw scores are standardized, so that scores range from 0 to 100. A high score indicates a high / healthy level of functioning. The responder is defined as having 10 points improvement from baseline confirmed by a second improvement of 10 points at any time, regardless of preceding worsening. A participant who could not improve was considered as a non-responder.
Analysis population: FAS comprised of all participants to whom study treatment had been assigned by randomization.
Groups in this outcome
Sabatolimab (MBG453) + Azacitidine
Participants were randomized to sabatolimab plus Azacitidine
Placebo + Azacitidine
Participants were randomized to placebo plus Azacitidine
| Group | Source count |
|---|---|
| Sabatolimab (MBG453) + Azacitidine | 265 |
| Placebo + Azacitidine | 265 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Sabatolimab (MBG453) + Azacitidine | 31.7 | Not reported | 26.1 | 37.7 | Not reported |
| Placebo + Azacitidine | 28.3 | Not reported | 23.0 | 34.1 | Not reported |
Source statistical analyses
- ci Lower Limit
- 0.8
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 1.7
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY
- p Value
- 0.2126
- p Value Comment
- P Value is 1-sided
- param Type
- Odds Ratio (OR)
- param Value
- 1.18
- statistical Comment
- exact CMH Chi-square statistic, adjusting for randomization stratification factor as per IRT.
- statistical Method
- Cochran-Mantel-Haenszel
Complete source fields
- analyses
- ci Lower Limit
- 0.8
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 1.7
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY
- p Value
- 0.2126
- p Value Comment
- P Value is 1-sided
- param Type
- Odds Ratio (OR)
- param Value
- 1.18
- statistical Comment
- exact CMH Chi-square statistic, adjusting for randomization stratification factor as per IRT.
- statistical Method
- Cochran-Mantel-Haenszel
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 26.1
- upper Limit
- 37.7
- value
- 31.7
- group Id
- OG001
- lower Limit
- 23.0
- upper Limit
- 34.1
- value
- 28.3
- denoms
- counts
- group Id
- OG000
- value
- 265
- group Id
- OG001
- value
- 265
- units
- Participants
- description
- EORTC-QLQ-C30 is a 30-item questionnaire developed to assess the quality of life of cancer participants. Participants' responses to 4 questions about their emotional functioning (Items 21-24) are scored on a 4-point scale (1=Not at All to 4=Very Much). Using linear transformation, raw scores are standardized, so that scores range from 0 to 100. A high score indicates a high / healthy level of functioning. The responder is defined as having 10 points improvement from baseline confirmed by a second improvement of 10 points at any time, regardless of preceding worsening. A participant who could not improve was considered as a non-responder.
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Participants were randomized to sabatolimab plus Azacitidine
- id
- OG000
- title
- Sabatolimab (MBG453) + Azacitidine
- description
- Participants were randomized to placebo plus Azacitidine
- id
- OG001
- title
- Placebo + Azacitidine
- param Type
- NUMBER
- population Description
- FAS comprised of all participants to whom study treatment had been assigned by randomization.
- reporting Status
- POSTED
- time Frame
- up to approx. 52 months
- title
- Key Secondary Endpoint 5: Percentage of Participants With at Least 10 Point Confirmed Improvement From Baseline in Emotional Functioning Using EORTC-QLQ-C30
- type
- SECONDARY
- unit Of Measure
- Percentage of participants
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Preserved source evidence · Not medical advice
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