TriangleNCT00405756 · OUTCOME
Kaplan Meier Estimates for Duration of Response as Determined by the Central Adjudication Committee (CAC)
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- weeks
- Interval / dispersion
- 95% Confidence Interval
- Time frame
- Up to 149 weeks
What was measured
Data as of 11 May 2010 cutoff. Duration of myeloma response was defined as the time from the initial response date to the earlier of progressive disease (PD) as determined by the CAC or death on study. PD was based on the European Group for Blood and Marrow Transplantation/International Bone Marrow Transplant Registry/Autologous Bone Marrow Transplant Registry \[EBMT/IBMTR/ABMTR\] criteria. PD criteria includes increasing monoclonal paraprotein levels, bone marrow findings, worsening lytic bone disease, progressively enlarging extramedullary plasmacytomas, or hypercalcemia.
Analysis population: Population: Participants who achieved a partial response (PR) or complete response (CR).
Groups in this outcome
MPR+R
Double-blind induction therapy with melphalan/prednisone and lenalidomide 10 mg (MPR) for up to 9 cycles, followed by maintenance therapy with single-agent lenalidomide (R) 10mg from cycle 10 to disease progression. Optional open-label extension therapy with lenalidomide up to 25 mg for participants with progressive disease.
MPR+p
Double-blind induction therapy with melphalan/prednisone and lenalidomide 10mg (MPR) for up to 9 cycles, followed by maintenance therapy with placebo (p) from cycle 10 to disease progression. Optional open-label extension therapy with lenalidomide up to 25 mg for participants with progressive disease.
MPp+p
Double-blind induction therapy with melphalan/prednisone and placebo (MPp) for up to 9 cycles, followed by maintenance therapy with placebo (p) from cycle 10 to disease progression. Optional open-label extension therapy with lenalidomide up to 25 mg for participants with progressive disease.
| Group | Source count |
|---|---|
| MPR+R | 117 |
| MPR+p | 104 |
| MPp+p | 77 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| MPR+R | 121.6 | Not reported | 96.00 | NA | Upper limit not estimable because of the number of participants without progressive disease at data cut-off. |
| MPR+p | 56.1 | Not reported | 52.14 | 64.29 | Not reported |
| MPp+p | 55.4 | Not reported | 44.14 | 76.14 | Not reported |
Source statistical analyses
- ci Lower Limit
- 0.228
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 0.531
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- p Value
- <0.001
- p Value Comment
- The p-value is based on unstratified log rank test of Kaplan Meier curve differences between the treatment groups.
- param Type
- Hazard Ratio (HR)
- param Value
- 0.348
- statistical Method
- Log Rank
- tested Non Inferiority
- false
- ci Lower Limit
- 0.281
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 0.623
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- p Value
- <0.001
- p Value Comment
- The p-value is based on unstratified log rank test of Kaplan Meier curve differences between the treatment groups.
- param Type
- Hazard Ratio (HR)
- param Value
- 0.419
- statistical Method
- Log Rank
- tested Non Inferiority
- false
- ci Lower Limit
- 0.571
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 1.191
- group Ids
- OG001
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- p Value
- 0.302
- p Value Comment
- The p-value is based on unstratified log rank test of Kaplan Meier curve differences between the treatment groups.
- param Type
- Hazard Ratio (HR)
- param Value
- 0.825
- statistical Method
- Log Rank
- tested Non Inferiority
- false
Complete source fields
- analyses
- ci Lower Limit
- 0.228
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 0.531
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- p Value
- <0.001
- p Value Comment
- The p-value is based on unstratified log rank test of Kaplan Meier curve differences between the treatment groups.
- param Type
- Hazard Ratio (HR)
- param Value
- 0.348
- statistical Method
- Log Rank
- tested Non Inferiority
- false
- ci Lower Limit
- 0.281
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 0.623
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- p Value
- <0.001
- p Value Comment
- The p-value is based on unstratified log rank test of Kaplan Meier curve differences between the treatment groups.
- param Type
- Hazard Ratio (HR)
- param Value
- 0.419
- statistical Method
- Log Rank
- tested Non Inferiority
- false
- ci Lower Limit
- 0.571
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 1.191
- group Ids
- OG001
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- p Value
- 0.302
- p Value Comment
- The p-value is based on unstratified log rank test of Kaplan Meier curve differences between the treatment groups.
- param Type
- Hazard Ratio (HR)
- param Value
- 0.825
- statistical Method
- Log Rank
- tested Non Inferiority
- false
- classes
- categories
- measurements
- comment
- Upper limit not estimable because of the number of participants without progressive disease at data cut-off.
- group Id
- OG000
- lower Limit
- 96.00
- upper Limit
- NA
- value
- 121.6
- group Id
- OG001
- lower Limit
- 52.14
- upper Limit
- 64.29
- value
- 56.1
- group Id
- OG002
- lower Limit
- 44.14
- upper Limit
- 76.14
- value
- 55.4
- denoms
- counts
- group Id
- OG000
- value
- 117
- group Id
- OG001
- value
- 104
- group Id
- OG002
- value
- 77
- units
- Participants
- description
- Data as of 11 May 2010 cutoff. Duration of myeloma response was defined as the time from the initial response date to the earlier of progressive disease (PD) as determined by the CAC or death on study. PD was based on the European Group for Blood and Marrow Transplantation/International Bone Marrow Transplant Registry/Autologous Bone Marrow Transplant Registry \[EBMT/IBMTR/ABMTR\] criteria. PD criteria includes increasing monoclonal paraprotein levels, bone marrow findings, worsening lytic bone disease, progressively enlarging extramedullary plasmacytomas, or hypercalcemia.
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Double-blind induction therapy with melphalan/prednisone and lenalidomide 10 mg (MPR) for up to 9 cycles, followed by maintenance therapy with single-agent lenalidomide (R) 10mg from cycle 10 to disease progression. Optional open-label extension therapy with lenalidomide up to 25 mg for participants with progressive disease.
- id
- OG000
- title
- MPR+R
- description
- Double-blind induction therapy with melphalan/prednisone and lenalidomide 10mg (MPR) for up to 9 cycles, followed by maintenance therapy with placebo (p) from cycle 10 to disease progression. Optional open-label extension therapy with lenalidomide up to 25 mg for participants with progressive disease.
- id
- OG001
- title
- MPR+p
- description
- Double-blind induction therapy with melphalan/prednisone and placebo (MPp) for up to 9 cycles, followed by maintenance therapy with placebo (p) from cycle 10 to disease progression. Optional open-label extension therapy with lenalidomide up to 25 mg for participants with progressive disease.
- id
- OG002
- title
- MPp+p
- param Type
- MEDIAN
- population Description
- Population: Participants who achieved a partial response (PR) or complete response (CR).
- reporting Status
- POSTED
- time Frame
- Up to 149 weeks
- title
- Kaplan Meier Estimates for Duration of Response as Determined by the Central Adjudication Committee (CAC)
- type
- SECONDARY
- unit Of Measure
- weeks
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Preserved source evidence · Not medical advice