NCT02186834 · OUTCOME
Overall Response Rate (ORR) - All Participants
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
- Up to 24 months
What was measured
ORR per the modified uniform response criteria of the International Myeloma Working Group (IMWG), partial response and better. Partial Remission (PR): \>/= 50% reduction of serum M-Protein and reduction in 24-hour urinary M-protein by \>/= 90% or to \< 200 mg per 24 hours; Very Good Partial Remission (VGPR): Serum and urine M-protein detectable by immunofixation but not on electrophoresis or 90% or greater reduction in serum M-protein plus urine M-protein level \<100 mg per 24 hours; Complete Remission (CR): Negative immunofixation on the serum and urine and disappearance of any soft tissue plasmacytomas and \</= 5% plasma cells in bone marrow. Stable Disease: Not meeting criteria for CR, VGPR, PR, or progressive disease. Minimal response: Less than 50% decrease in M protein. Not evaluable: Cannot be measured because enough information has not been collected.
Analysis population: All participants
Groups in this outcome
Selinexor, Liposomal Doxorubicin and Dexamethasone
Combination Therapy: Phase I Dose Escalation followed by Phase 2 treatment at Recommended Phase 2 Dose (RP2D)
| Group | Source count |
|---|---|
| Selinexor, Liposomal Doxorubicin and Dexamethasone | 27 |
Reported measurements
>/= Very Good Partial Response
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Selinexor, Liposomal Doxorubicin and Dexamethasone | 2 | Not reported | Not reported | Not reported | Not reported |
>/= Partial Response
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Selinexor, Liposomal Doxorubicin and Dexamethasone | 4 | Not reported | Not reported | Not reported | Not reported |
>/= Minimal Response
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Selinexor, Liposomal Doxorubicin and Dexamethasone | 9 | Not reported | Not reported | Not reported | Not reported |
Stable Disease
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Selinexor, Liposomal Doxorubicin and Dexamethasone | 8 | Not reported | Not reported | Not reported | Not reported |
Not Evaluable
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Selinexor, Liposomal Doxorubicin and Dexamethasone | 4 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 2
- title
- >/= Very Good Partial Response
- categories
- measurements
- group Id
- OG000
- value
- 4
- title
- >/= Partial Response
- categories
- measurements
- group Id
- OG000
- value
- 9
- title
- >/= Minimal Response
- categories
- measurements
- group Id
- OG000
- value
- 8
- title
- Stable Disease
- categories
- measurements
- group Id
- OG000
- value
- 4
- title
- Not Evaluable
- denoms
- counts
- group Id
- OG000
- value
- 27
- units
- Participants
- description
- ORR per the modified uniform response criteria of the International Myeloma Working Group (IMWG), partial response and better. Partial Remission (PR): \>/= 50% reduction of serum M-Protein and reduction in 24-hour urinary M-protein by \>/= 90% or to \< 200 mg per 24 hours; Very Good Partial Remission (VGPR): Serum and urine M-protein detectable by immunofixation but not on electrophoresis or 90% or greater reduction in serum M-protein plus urine M-protein level \<100 mg per 24 hours; Complete Remission (CR): Negative immunofixation on the serum and urine and disappearance of any soft tissue plasmacytomas and \</= 5% plasma cells in bone marrow. Stable Disease: Not meeting criteria for CR, VGPR, PR, or progressive disease. Minimal response: Less than 50% decrease in M protein. Not evaluable: Cannot be measured because enough information has not been collected.
- groups
- description
- Combination Therapy: Phase I Dose Escalation followed by Phase 2 treatment at Recommended Phase 2 Dose (RP2D)
- id
- OG000
- title
- Selinexor, Liposomal Doxorubicin and Dexamethasone
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- All participants
- reporting Status
- POSTED
- time Frame
- Up to 24 months
- title
- Overall Response Rate (ORR) - All Participants
- type
- PRIMARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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