NCT00891904 · OUTCOME
Overall Survival
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- Not reported
- Unit
- Not reported
- Interval / dispersion
- Not reported
- Time frame
- very 2 months for year one, every 3-4 months for year 2, every 6 months for years 3 and 4 and annually thereafter
Analysis population: Trial terminated early. Too few patients to analyze.
Groups in this outcome
Biological/Vaccine: Cetuximab
All patients enrolled will receive cetuximab 400 mg/m 2 IV x 1 dose 1 week prior to delivery of SBRT. Patients will then receive 15 Gy x 1 using SBRT and cetuximab i.v. 250 mg/m2 weekly for 4 weeks (total of 5 doses at 250 mg/m2).
| Group | Source count |
|---|---|
| Biological/Vaccine: Cetuximab | 0 |
Reported measurements
No numerical measurement classes were posted for this outcome. Missing is not zero.
Complete source fields
- denoms
- counts
- group Id
- OG000
- value
- 0
- units
- Participants
- groups
- description
- All patients enrolled will receive cetuximab 400 mg/m 2 IV x 1 dose 1 week prior to delivery of SBRT. Patients will then receive 15 Gy x 1 using SBRT and cetuximab i.v. 250 mg/m2 weekly for 4 weeks (total of 5 doses at 250 mg/m2).
- id
- OG000
- title
- Biological/Vaccine: Cetuximab
- population Description
- Trial terminated early. Too few patients to analyze.
- reporting Status
- POSTED
- time Frame
- very 2 months for year one, every 3-4 months for year 2, every 6 months for years 3 and 4 and annually thereafter
- title
- Overall Survival
- type
- SECONDARY
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle