NCT05011058 · OUTCOME
Overall Survival (OS)
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- days
- Interval / dispersion
- Full Range
- Time frame
- Up to approximately 3 years
What was measured
Interval of time from the start of study drug treatment to the date of death for any reason. OS was censored at the time of study withdrawal or study termination, whichever was earlier, for patients without reported death.
Analysis population: Intent-to-Treat Analysis Set, defined as all patients who were enrolled into the trial regardless of whether or not they received study treatment. The study was not designed to make formal statistical comparisons of OS between cohorts.
Groups in this outcome
Diffuse Large B-Cell Lymphoma
Patients with relapsed or refractory EBV-positive diffuse large B-cell lymphoma treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
Extranodal Natural Killer/T-Cell Lymphoma
Patients with relapsed or refractory EBV-positive extranodal natural killer/T-cell lymphoma treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
Peripheral T-Cell Lymphoma (Combination Therapy)
Patients with relapsed or refractory EBV-positive angioimmunoblastic T-cell lymphoma or peripheral T-cell lymphoma not otherwise specified treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
Peripheral T-Cell Lymphoma (Monotherapy)
Patients with relapsed or refractory EBV-positive angioimmunoblastic T-cell lymphoma or peripheral T-cell lymphoma not otherwise specified treated with nanatinostat 20 mg QD on Days 1 to 4 per week
Hodgkin Lymphoma
Patients with relapsed or refractory EBV-positive Hodgkin lymphoma treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
Post-Transplant Lymphoproliferative Disorders
Patients with relapsed or refractory EBV-positive post-transplant lymphoproliferative disorders treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
Human Immunodeficiency Virus-Associated Lymphomas
Patients with relapsed or refractory EBV-positive human immunodeficiency virus-associated lymphomas treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
Other EBV-Positive Lymphomas
Patients with relapsed or refractory EBV-positive lymphomas other than those from the other cohorts treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
| Group | Source count |
|---|---|
| Diffuse Large B-Cell Lymphoma | 9 |
| Extranodal Natural Killer/T-Cell Lymphoma | 11 |
| Peripheral T-Cell Lymphoma (Combination Therapy) | 38 |
| Peripheral T-Cell Lymphoma (Monotherapy) | 10 |
| Hodgkin Lymphoma | 8 |
| Post-Transplant Lymphoproliferative Disorders | 3 |
| Human Immunodeficiency Virus-Associated Lymphomas | 3 |
| Other EBV-Positive Lymphomas | 20 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Diffuse Large B-Cell Lymphoma | 131 | Not reported | 29 | 242 | Not reported |
| Extranodal Natural Killer/T-Cell Lymphoma | 243 | Not reported | 35 | 517 | Not reported |
| Peripheral T-Cell Lymphoma (Combination Therapy) | 221 | Not reported | 14 | 730 | Not reported |
| Peripheral T-Cell Lymphoma (Monotherapy) | 155 | Not reported | 41 | 611 | Not reported |
| Hodgkin Lymphoma | 570.5 | Not reported | 64 | 1000 | Not reported |
| Post-Transplant Lymphoproliferative Disorders | 171 | Not reported | 36 | 351 | Not reported |
| Human Immunodeficiency Virus-Associated Lymphomas | 108 | Not reported | 76 | 296 | Not reported |
| Other EBV-Positive Lymphomas | 167.5 | Not reported | 35 | 513 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 29
- upper Limit
- 242
- value
- 131
- group Id
- OG001
- lower Limit
- 35
- upper Limit
- 517
- value
- 243
- group Id
- OG002
- lower Limit
- 14
- upper Limit
- 730
- value
- 221
- group Id
- OG003
- lower Limit
- 41
- upper Limit
- 611
- value
- 155
- group Id
- OG004
- lower Limit
- 64
- upper Limit
- 1000
- value
- 570.5
- group Id
- OG005
- lower Limit
- 36
- upper Limit
- 351
- value
- 171
- group Id
- OG006
- lower Limit
- 76
- upper Limit
- 296
- value
- 108
- group Id
- OG007
- lower Limit
- 35
- upper Limit
- 513
- value
- 167.5
- denoms
- counts
- group Id
- OG000
- value
- 9
- group Id
- OG001
- value
- 11
- group Id
- OG002
- value
- 38
- group Id
- OG003
- value
- 10
- group Id
- OG004
- value
- 8
- group Id
- OG005
- value
- 3
- group Id
- OG006
- value
- 3
- group Id
- OG007
- value
- 20
- units
- Participants
- description
- Interval of time from the start of study drug treatment to the date of death for any reason. OS was censored at the time of study withdrawal or study termination, whichever was earlier, for patients without reported death.
- dispersion Type
- Full Range
- groups
- description
- Patients with relapsed or refractory EBV-positive diffuse large B-cell lymphoma treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
- id
- OG000
- title
- Diffuse Large B-Cell Lymphoma
- description
- Patients with relapsed or refractory EBV-positive extranodal natural killer/T-cell lymphoma treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
- id
- OG001
- title
- Extranodal Natural Killer/T-Cell Lymphoma
- description
- Patients with relapsed or refractory EBV-positive angioimmunoblastic T-cell lymphoma or peripheral T-cell lymphoma not otherwise specified treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
- id
- OG002
- title
- Peripheral T-Cell Lymphoma (Combination Therapy)
- description
- Patients with relapsed or refractory EBV-positive angioimmunoblastic T-cell lymphoma or peripheral T-cell lymphoma not otherwise specified treated with nanatinostat 20 mg QD on Days 1 to 4 per week
- id
- OG003
- title
- Peripheral T-Cell Lymphoma (Monotherapy)
- description
- Patients with relapsed or refractory EBV-positive Hodgkin lymphoma treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
- id
- OG004
- title
- Hodgkin Lymphoma
- description
- Patients with relapsed or refractory EBV-positive post-transplant lymphoproliferative disorders treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
- id
- OG005
- title
- Post-Transplant Lymphoproliferative Disorders
- description
- Patients with relapsed or refractory EBV-positive human immunodeficiency virus-associated lymphomas treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
- id
- OG006
- title
- Human Immunodeficiency Virus-Associated Lymphomas
- description
- Patients with relapsed or refractory EBV-positive lymphomas other than those from the other cohorts treated with nanatinostat 20 mg QD on Days 1 to 4 per week and valganciclovir 900 mg QD
- id
- OG007
- title
- Other EBV-Positive Lymphomas
- param Type
- MEDIAN
- population Description
- Intent-to-Treat Analysis Set, defined as all patients who were enrolled into the trial regardless of whether or not they received study treatment. The study was not designed to make formal statistical comparisons of OS between cohorts.
- reporting Status
- POSTED
- time Frame
- Up to approximately 3 years
- title
- Overall Survival (OS)
- type
- SECONDARY
- unit Of Measure
- days
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