NCT00749892 · OUTCOME
Response Rate
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
- Determined at the time of surgery or cystectomy
What was measured
The response rate is the number of patients with urothelial cancer treated with erlotinib prior to cystectomy. The response is defined as the absence of residual cancer in the surgical removed tissue (i.e., pT0). A responder is defined as a participant with the pathological stage of pT0 meaning that there is no evidence of disease.
Analysis population: two participants did not take any eroltinib and three participants stopped erlotinib early due to intolerable side effects.
Groups in this outcome
Pre-surgical Erlotinib Treatment
Erlotinib 150 mg by mouth daily for 3 weeks followed by cystectomy within 24 hours of the last dose.
| Group | Source count |
|---|---|
| Pre-surgical Erlotinib Treatment | 26 |
Reported measurements
Number of Responders
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Pre-surgical Erlotinib Treatment | 8 | Not reported | Not reported | Not reported | Not reported |
Number of Non Responders
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Pre-surgical Erlotinib Treatment | 18 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 8
- title
- Number of Responders
- categories
- measurements
- group Id
- OG000
- value
- 18
- title
- Number of Non Responders
- denoms
- counts
- group Id
- OG000
- value
- 26
- units
- Participants
- description
- The response rate is the number of patients with urothelial cancer treated with erlotinib prior to cystectomy. The response is defined as the absence of residual cancer in the surgical removed tissue (i.e., pT0). A responder is defined as a participant with the pathological stage of pT0 meaning that there is no evidence of disease.
- groups
- description
- Erlotinib 150 mg by mouth daily for 3 weeks followed by cystectomy within 24 hours of the last dose.
- id
- OG000
- title
- Pre-surgical Erlotinib Treatment
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- two participants did not take any eroltinib and three participants stopped erlotinib early due to intolerable side effects.
- reporting Status
- POSTED
- time Frame
- Determined at the time of surgery or cystectomy
- title
- Response Rate
- type
- PRIMARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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