NCT00571662 · OUTCOME
Toxicity for the Combination of Pentostatin and Low Dose Total Body Irradiation (TBI)
Safety and Efficacy of Pentostatin and Low Dose TBI With Allogenic Peripheral Blood Stem Cell Transplant · Source last updated 2023-10-24
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- COUNT_OF_PARTICIPANTS
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- Conditioning regimen to count recovery (D + 28 post transplant)
Groups in this outcome
Cohort I
Pentostatin to be administered intravenously on days -10, -9, and -8 at a dose of 4mg/m2/day
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| Cohort I | 68 |
|---|
Reported measurements
Absolute neutrophil count < 500/mm^3
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 40 | Not reported | Not reported | Not reported | Not reported |
|---|
platelet count < 20,000/mm^3
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 29 | Not reported | Not reported | Not reported | Not reported |
|---|
Grade 3 or 4 Fever
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 2 | Not reported | Not reported | Not reported | Not reported |
|---|
Grade 3 or 4 hypokalemia
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Grade 3 or 4 bacteremia
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 2 | Not reported | Not reported | Not reported | Not reported |
|---|
Grade 3 or 4 infection
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 6 | Not reported | Not reported | Not reported | Not reported |
|---|
Grade 3 or 4 renal toxicity
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Grade 3 or 4 thromboembolism
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Cohort I | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- title
- Absolute neutrophil count < 500/mm^3
- title
- platelet count < 20,000/mm^3
- title
- Grade 3 or 4 Fever
- title
- Grade 3 or 4 hypokalemia
- title
- Grade 3 or 4 bacteremia
- title
- Grade 3 or 4 infection
- title
- Grade 3 or 4 renal toxicity
- title
- Grade 3 or 4 thromboembolism
- groups
- description
- Pentostatin to be administered intravenously on days -10, -9, and -8 at a dose of 4mg/m2/day
- id
- OG000
- title
- Cohort I
- param Type
- COUNT_OF_PARTICIPANTS
- reporting Status
- POSTED
- time Frame
- Conditioning regimen to count recovery (D + 28 post transplant)
- title
- Toxicity for the Combination of Pentostatin and Low Dose Total Body Irradiation (TBI)
- type
- PRIMARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice