NCT00061945 · OUTCOME
Number of Participants Achieving Complete Remission
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- participants
- Interval / dispersion
- Not reported
- Time frame
- 9 years
What was measured
A complete remission (CR) requires the following: an absolute neutrophil count (segs and bands) \> 1500/μl, no circulating blasts, platelets \> 100,000/μl; bone marrow cellularity \> 20% with trilineage hematopoiesis, and \< 5% marrow blast cells, none of which appear neoplastic. All previous extramedullary manifestations of disease must be absent (e.g., lymphadenopathy, splenomegaly, skin or gum infiltration, testicular masses, or CNS involvement).
Analysis population: Three participants were deemed ineligible and excluded from this analysis.
Groups in this outcome
Phase I - Alemtuzumab and Combination Chemotherapy
See detailed description
Phase II - Alemtuzumab and Combination Chemotherapy
See detailed description
| Group | Source count |
|---|---|
| Phase I - Alemtuzumab and Combination Chemotherapy | 116 |
| Phase II - Alemtuzumab and Combination Chemotherapy | 181 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Phase I - Alemtuzumab and Combination Chemotherapy | 92 | Not reported | Not reported | Not reported | Not reported |
| Phase II - Alemtuzumab and Combination Chemotherapy | 145 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 92
- group Id
- OG001
- value
- 145
- denoms
- counts
- group Id
- OG000
- value
- 116
- group Id
- OG001
- value
- 181
- units
- Participants
- description
- A complete remission (CR) requires the following: an absolute neutrophil count (segs and bands) \> 1500/μl, no circulating blasts, platelets \> 100,000/μl; bone marrow cellularity \> 20% with trilineage hematopoiesis, and \< 5% marrow blast cells, none of which appear neoplastic. All previous extramedullary manifestations of disease must be absent (e.g., lymphadenopathy, splenomegaly, skin or gum infiltration, testicular masses, or CNS involvement).
- groups
- description
- See detailed description
- id
- OG000
- title
- Phase I - Alemtuzumab and Combination Chemotherapy
- description
- See detailed description
- id
- OG001
- title
- Phase II - Alemtuzumab and Combination Chemotherapy
- param Type
- NUMBER
- population Description
- Three participants were deemed ineligible and excluded from this analysis.
- reporting Status
- POSTED
- time Frame
- 9 years
- title
- Number of Participants Achieving Complete Remission
- type
- POST_HOC
- unit Of Measure
- participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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