NCT04266301 · OUTCOME
Key Secondary Endpoint 4: Percentage of Participants With at Least 10 Point Confirmed Improvement From Baseline in Physical Functioning Using European Organization for Research and Treatment of Cancer's Core Quality of Life Questionnaire (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 with response
- 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 5 questions about their physical functioning (Items 1-5) 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 | 30.2 | Not reported | 24.7 | 36.1 | Not reported |
| Placebo + Azacitidine | 22.6 | Not reported | 17.7 | 28.2 | Not reported |
Source statistical analyses
- ci Lower Limit
- 1
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 2.2
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY
- p Value
- 0.5743
- p Value Comment
- P Value is 1-sided
- param Type
- Odds Ratio (OR)
- param Value
- 1.48
- 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
- 1
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 2.2
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY
- p Value
- 0.5743
- p Value Comment
- P Value is 1-sided
- param Type
- Odds Ratio (OR)
- param Value
- 1.48
- 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
- 24.7
- upper Limit
- 36.1
- value
- 30.2
- group Id
- OG001
- lower Limit
- 17.7
- upper Limit
- 28.2
- value
- 22.6
- 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 5 questions about their physical functioning (Items 1-5) 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 4: Percentage of Participants With at Least 10 Point Confirmed Improvement From Baseline in Physical Functioning Using European Organization for Research and Treatment of Cancer's Core Quality of Life Questionnaire (EORTC QLQ-C30)
- type
- SECONDARY
- unit Of Measure
- Percentage of participants with response
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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