NCT00095563 · OUTCOME
Rate of Stable Disease
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
- 6 months
What was measured
Number of patients who had Stable disease for more than or equal to 6 months together in both Adenoid cystic carcinoma (ACC) and non-adenoid cyctic carcinoma (non-ACC)
Analysis population: 36 assessable participants, 19 with ACC and 17 with non-ACC.
Groups in this outcome
Treatment (Lapatinib Ditosylate)
Patients receive oral lapatinib once daily on days 1-28. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression. lapatinib ditosylate: Given orally laboratory biomarker analysis: Correlative studies
| Group | Source count |
|---|---|
| Treatment (Lapatinib Ditosylate) | 36 |
Reported measurements
ACC
| Group | Source count |
|---|---|
| Treatment (Lapatinib Ditosylate) | 19 |
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Treatment (Lapatinib Ditosylate) | 9 | Not reported | Not reported | Not reported | Not reported |
Non-ACC
| Group | Source count |
|---|---|
| Treatment (Lapatinib Ditosylate) | 17 |
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Treatment (Lapatinib Ditosylate) | 4 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 9
- denoms
- counts
- group Id
- OG000
- value
- 19
- units
- Participants
- title
- ACC
- categories
- measurements
- group Id
- OG000
- value
- 4
- denoms
- counts
- group Id
- OG000
- value
- 17
- units
- Participants
- title
- Non-ACC
- denoms
- counts
- group Id
- OG000
- value
- 36
- units
- Participants
- description
- Number of patients who had Stable disease for more than or equal to 6 months together in both Adenoid cystic carcinoma (ACC) and non-adenoid cyctic carcinoma (non-ACC)
- groups
- description
- Patients receive oral lapatinib once daily on days 1-28. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression. lapatinib ditosylate: Given orally laboratory biomarker analysis: Correlative studies
- id
- OG000
- title
- Treatment (Lapatinib Ditosylate)
- param Type
- NUMBER
- population Description
- 36 assessable participants, 19 with ACC and 17 with non-ACC.
- reporting Status
- POSTED
- time Frame
- 6 months
- title
- Rate of Stable Disease
- type
- SECONDARY
- unit Of Measure
- participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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