NCT00566696 · OUTCOME
To Estimate the Cumulative Incidence of Relapse for Research Participants Who Receive This Study Treatment.
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
- Not reported
- Time frame
- five years post-transplant
What was measured
The Cumulative Incidence of Relapse will be reported as the proportion of number of relapses since transplant to the total number of patients at risk at five years post-transplant.
Groups in this outcome
High-Risk Hematologic Malignancies
Participants meeting eligibility criteria and who underwent haploidentical stem cell transplantation with systemic chemotherapy and antibodies, including Fludarabine, Thioplex®, L-phenylalanine mustard, mycophenolate mofetil, CellCept®, Rituxan™, Muromonab (prior to January 2010) or Alemtuzumab (beginning January 2010), Cyclophosphamide, Anti-thymocyte globulin (Rabbit), and G-CSF.
| Group | Source count |
|---|---|
| High-Risk Hematologic Malignancies | 31 |
Reported measurements
The Cumulative Incidence of Relapse at five year p
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| High-Risk Hematologic Malignancies | 30.0 | Not reported | Not reported | Not reported | Not reported |
Estimate±SE
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| High-Risk Hematologic Malignancies | 8.6 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 30.0
- title
- The Cumulative Incidence of Relapse at five year p
- categories
- measurements
- group Id
- OG000
- value
- 8.6
- title
- Estimate±SE
- denoms
- counts
- group Id
- OG000
- value
- 31
- units
- Participants
- description
- The Cumulative Incidence of Relapse will be reported as the proportion of number of relapses since transplant to the total number of patients at risk at five years post-transplant.
- groups
- description
- Participants meeting eligibility criteria and who underwent haploidentical stem cell transplantation with systemic chemotherapy and antibodies, including Fludarabine, Thioplex®, L-phenylalanine mustard, mycophenolate mofetil, CellCept®, Rituxan™, Muromonab (prior to January 2010) or Alemtuzumab (beginning January 2010), Cyclophosphamide, Anti-thymocyte globulin (Rabbit), and G-CSF.
- id
- OG000
- title
- High-Risk Hematologic Malignancies
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- five years post-transplant
- title
- To Estimate the Cumulative Incidence of Relapse for Research Participants Who Receive This Study Treatment.
- type
- SECONDARY
- unit Of Measure
- Percentage of participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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