TriangleNCT00829166 · OUTCOME
Percentage of Participants Who Died: Final Analysis
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
- From the date of randomization through the data cut-off date of 31 Dec 2014 (up to 5 years, 11 months)
What was measured
The percentage of participants who died from any cause was reported. The results reported are from the final analysis. The final analysis is descriptive.
Analysis population: ITT population included all randomized participants on the basis of the treatment assigned at randomization.
Groups in this outcome
Trastuzumab Emtansine
Participants received trastuzumab emtansine 3.6 mg/kg IV infusion over 30-90 minutes on Day 1 of each 21-day treatment cycle until PD (as assessed by the investigator), unmanageable toxicity, or study termination.
Lapatinib + Capecitabine
Participants received lapatinib 1250 mg (five 250 mg tablets) orally once daily during each 21-day cycle + capecitabine 1000 mg/m\^2 orally twice daily on Days 1-14 of each 21-day treatment cycle until PD (as assessed by the investigator), unmanageable toxicity, or study termination. Participants of this group were allowed to cross over to receive trastuzumab emtansine based on statistically significant OS benefit in favor of trastuzumab emtansine demonstrated in second interim analysis.
| Group | Source count |
|---|---|
| Trastuzumab Emtansine | 495 |
| Lapatinib + Capecitabine | 496 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Trastuzumab Emtansine | 61.2 | Not reported | Not reported | Not reported | Not reported |
| Lapatinib + Capecitabine | 67.1 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 61.2
- group Id
- OG001
- value
- 67.1
- denoms
- counts
- group Id
- OG000
- value
- 495
- group Id
- OG001
- value
- 496
- units
- Participants
- description
- The percentage of participants who died from any cause was reported. The results reported are from the final analysis. The final analysis is descriptive.
- groups
- description
- Participants received trastuzumab emtansine 3.6 mg/kg IV infusion over 30-90 minutes on Day 1 of each 21-day treatment cycle until PD (as assessed by the investigator), unmanageable toxicity, or study termination.
- id
- OG000
- title
- Trastuzumab Emtansine
- description
- Participants received lapatinib 1250 mg (five 250 mg tablets) orally once daily during each 21-day cycle + capecitabine 1000 mg/m\^2 orally twice daily on Days 1-14 of each 21-day treatment cycle until PD (as assessed by the investigator), unmanageable toxicity, or study termination. Participants of this group were allowed to cross over to receive trastuzumab emtansine based on statistically significant OS benefit in favor of trastuzumab emtansine demonstrated in second interim analysis.
- id
- OG001
- title
- Lapatinib + Capecitabine
- param Type
- NUMBER
- population Description
- ITT population included all randomized participants on the basis of the treatment assigned at randomization.
- reporting Status
- POSTED
- time Frame
- From the date of randomization through the data cut-off date of 31 Dec 2014 (up to 5 years, 11 months)
- title
- Percentage of Participants Who Died: Final Analysis
- type
- PRIMARY
- unit Of Measure
- percentage of participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice