NCT00777036 · OUTCOME
Major Cytogenetic Response (MCyR) Rate in Cohort 2
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
- From first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)
What was measured
Major Cytogenetic Response (MCyR) rate was defined as the proportion of all treated participants who achieved a complete (0%) or partial (1%-35% Ph+ metaphases in at least 20 metaphases in bone marrow) cytogenetic response. The percentage of treated participants in each arm with MCyR is reported.
Analysis population: Secondary efficacy endpoint pre-specified only for participants treated in Cohort 2
Groups in this outcome
Cohort 2
Children and adolescents with Ph+ ALL, AP-CML or BP-CML who were resistant or intolerant to, or relapsed after imatinib therapy received dasatinib tablets at a dose schedule of 80 mg/m2 QD on a continuous oral regimen.
| Group | Source count |
|---|---|
| Cohort 2 | 17 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Cohort 2 | 52.9 | Not reported | 27.8 | 77.0 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 27.8
- upper Limit
- 77.0
- value
- 52.9
- denoms
- counts
- group Id
- OG000
- value
- 17
- units
- Participants
- description
- Major Cytogenetic Response (MCyR) rate was defined as the proportion of all treated participants who achieved a complete (0%) or partial (1%-35% Ph+ metaphases in at least 20 metaphases in bone marrow) cytogenetic response. The percentage of treated participants in each arm with MCyR is reported.
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Children and adolescents with Ph+ ALL, AP-CML or BP-CML who were resistant or intolerant to, or relapsed after imatinib therapy received dasatinib tablets at a dose schedule of 80 mg/m2 QD on a continuous oral regimen.
- id
- OG000
- title
- Cohort 2
- param Type
- NUMBER
- population Description
- Secondary efficacy endpoint pre-specified only for participants treated in Cohort 2
- reporting Status
- POSTED
- time Frame
- From first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)
- title
- Major Cytogenetic Response (MCyR) Rate in Cohort 2
- type
- SECONDARY
- unit Of Measure
- percentage of participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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