NCT01332968 · OUTCOME
Change From Baseline in FACT-Lym Individual Subscale Lymphoma Score (Follicular Population)
A Study of Obinutuzumab (RO5072759) Plus Chemotherapy in Comparison With Rituximab Plus Chemotherapy Followed by Obinutuzumab or Rituximab Maintenance in Patients With Untreated Advanced Indolent Non-Hodgkin's Lymphoma (GALLIUM) · Source last updated 2022-08-11
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEAN
- Unit
- units on a scale
- Interval / dispersion
- Standard Deviation
- Time frame
- Baseline (Induction Cycle 1, Day 1), data cut-off (up to approximately 5 years and 2 months)
What was measured
The FACT-Lym Individual Subscale Lymphoma Score for the follicular lymphoma population was derived from the Lymphoma subscale questionnaire (range: 0-60). Higher scores indicate better outcomes. A positive change from baseline indicates an improvement.
Analysis population: The FL ITT population was defined as all randomized participants with follicular histology grouped according to their randomized treatment arm regardless of what treatments were actually received.
Groups in this outcome
Rituximab+Chemotherapy
Participants received either 8 cycles of rituximab along with 6 cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) (21-day cycle) or 8 cycles of rituximab along with 8 cycles of cyclophosphamide, vincristine, and prednisone (CVP) (21-day cycles) or 6 cycles of rituximab along with 6 cycles of bendamustine (28-day cycle) during the induction period. The induction period was followed by either a maintenance or observation period for responders or non-responders, respectively. Responders received rituximab monotherapy every 2 months for 2 years during the maintenance period. Non-responders received no protocol specified treatment during the 2-year observation period. Finally, participants were followed during a 5-year follow-up period. The chemotherapy regimen (CHOP or CVP or bendamustine) for individual participant was chosen by the site prior to initiation of the study.
Obinutuzumab+Chemotherapy
Participants received either 8 cycles of obinutuzumab along with 6 cycles of CHOP (21-day cycle) or 8 cycles of obinutuzumab along with 8 cycles of CVP (21-day cycles) or 6 cycles of obinutuzumab along with 6 cycles of bendamustine (28-day cycle) during induction period. The induction period was followed by either a maintenance or observation period for responders or non-responders, respectively. Responders received obinutuzumab monotherapy every 2 months for 2 years during the maintenance period. Non-responders received no protocol specified treatment during the 2-year observation period. Finally, participants were followed during a 5-year follow-up period. The chemotherapy regimen (CHOP or CVP or bendamustine) for individual participant was chosen by the site prior to initiation of the study.
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| Rituximab+Chemotherapy | 556 |
|---|
| Obinutuzumab+Chemotherapy | 563 |
|---|
Reported measurements
Lymphoma, Baseline
Analysis denominator · Participants
| Group | Source count |
|---|
| Rituximab+Chemotherapy | 556 |
|---|
| Obinutuzumab+Chemotherapy | 563 |
|---|
Values in units on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rituximab+Chemotherapy | 45.01 | 9.37 | Not reported | Not reported | Not reported |
|---|
| Obinutuzumab+Chemotherapy | 45.54 | 9.29 | Not reported | Not reported | Not reported |
|---|
Lymphoma Change, Cycle 3 Day 1
Analysis denominator · Participants
| Group | Source count |
|---|
| Rituximab+Chemotherapy | 509 |
|---|
| Obinutuzumab+Chemotherapy | 491 |
|---|
Values in units on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rituximab+Chemotherapy | 2.04 | 7.18 | Not reported | Not reported | Not reported |
|---|
| Obinutuzumab+Chemotherapy | 2.71 | 7.46 | Not reported | Not reported | Not reported |
|---|
Lymphoma Change, End Induction
Analysis denominator · Participants
| Group | Source count |
|---|
| Rituximab+Chemotherapy | 477 |
|---|
| Obinutuzumab+Chemotherapy | 478 |
|---|
Values in units on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rituximab+Chemotherapy | 2.99 | 8.63 | Not reported | Not reported | Not reported |
|---|
| Obinutuzumab+Chemotherapy | 3.01 | 8.36 | Not reported | Not reported | Not reported |
|---|
Lymphoma Change, Maint Month 2
Analysis denominator · Participants
| Group | Source count |
|---|
| Rituximab+Chemotherapy | 360 |
|---|
| Obinutuzumab+Chemotherapy | 395 |
|---|
Values in units on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rituximab+Chemotherapy | 4.80 | 8.29 | Not reported | Not reported | Not reported |
|---|
| Obinutuzumab+Chemotherapy | 4.52 | 8.32 | Not reported | Not reported | Not reported |
|---|
Lymphoma Change, Maint Month 12
Analysis denominator · Participants
| Group | Source count |
|---|
| Rituximab+Chemotherapy | 360 |
|---|
| Obinutuzumab+Chemotherapy | 404 |
|---|
Values in units on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rituximab+Chemotherapy | 4.93 | 8.34 | Not reported | Not reported | Not reported |
|---|
| Obinutuzumab+Chemotherapy | 4.27 | 8.31 | Not reported | Not reported | Not reported |
|---|
Lymphoma Change, End Maint
Analysis denominator · Participants
| Group | Source count |
|---|
| Rituximab+Chemotherapy | 407 |
|---|
| Obinutuzumab+Chemotherapy | 438 |
|---|
Values in units on a scale · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rituximab+Chemotherapy | 4.31 | 8.81 | Not reported | Not reported | Not reported |
|---|
| Obinutuzumab+Chemotherapy | 4.57 | 8.54 | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 9.37
- value
- 45.01
- group Id
- OG001
- spread
- 9.29
- value
- 45.54
- denoms
- counts
- group Id
- OG000
- value
- 556
- group Id
- OG001
- value
- 563
- units
- Participants
- title
- Lymphoma, Baseline
- categories
- measurements
- group Id
- OG000
- spread
- 7.18
- value
- 2.04
- group Id
- OG001
- spread
- 7.46
- value
- 2.71
- denoms
- counts
- group Id
- OG000
- value
- 509
- group Id
- OG001
- value
- 491
- units
- Participants
- title
- Lymphoma Change, Cycle 3 Day 1
- categories
- measurements
- group Id
- OG000
- spread
- 8.63
- value
- 2.99
- group Id
- OG001
- spread
- 8.36
- value
- 3.01
- denoms
- counts
- group Id
- OG000
- value
- 477
- group Id
- OG001
- value
- 478
- units
- Participants
- title
- Lymphoma Change, End Induction
- categories
- measurements
- group Id
- OG000
- spread
- 8.29
- value
- 4.80
- group Id
- OG001
- spread
- 8.32
- value
- 4.52
- denoms
- counts
- group Id
- OG000
- value
- 360
- group Id
- OG001
- value
- 395
- units
- Participants
- title
- Lymphoma Change, Maint Month 2
- categories
- measurements
- group Id
- OG000
- spread
- 8.34
- value
- 4.93
- group Id
- OG001
- spread
- 8.31
- value
- 4.27
- denoms
- counts
- group Id
- OG000
- value
- 360
- group Id
- OG001
- value
- 404
- units
- Participants
- title
- Lymphoma Change, Maint Month 12
- categories
- measurements
- group Id
- OG000
- spread
- 8.81
- value
- 4.31
- group Id
- OG001
- spread
- 8.54
- value
- 4.57
- denoms
- counts
- group Id
- OG000
- value
- 407
- group Id
- OG001
- value
- 438
- units
- Participants
- title
- Lymphoma Change, End Maint
- denoms
- counts
- group Id
- OG000
- value
- 556
- group Id
- OG001
- value
- 563
- units
- Participants
- description
- The FACT-Lym Individual Subscale Lymphoma Score for the follicular lymphoma population was derived from the Lymphoma subscale questionnaire (range: 0-60). Higher scores indicate better outcomes. A positive change from baseline indicates an improvement.
- dispersion Type
- Standard Deviation
- groups
- description
- Participants received either 8 cycles of rituximab along with 6 cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) (21-day cycle) or 8 cycles of rituximab along with 8 cycles of cyclophosphamide, vincristine, and prednisone (CVP) (21-day cycles) or 6 cycles of rituximab along with 6 cycles of bendamustine (28-day cycle) during the induction period. The induction period was followed by either a maintenance or observation period for responders or non-responders, respectively. Responders received rituximab monotherapy every 2 months for 2 years during the maintenance period. Non-responders received no protocol specified treatment during the 2-year observation period. Finally, participants were followed during a 5-year follow-up period. The chemotherapy regimen (CHOP or CVP or bendamustine) for individual participant was chosen by the site prior to initiation of the study.
- id
- OG000
- title
- Rituximab+Chemotherapy
- description
- Participants received either 8 cycles of obinutuzumab along with 6 cycles of CHOP (21-day cycle) or 8 cycles of obinutuzumab along with 8 cycles of CVP (21-day cycles) or 6 cycles of obinutuzumab along with 6 cycles of bendamustine (28-day cycle) during induction period. The induction period was followed by either a maintenance or observation period for responders or non-responders, respectively. Responders received obinutuzumab monotherapy every 2 months for 2 years during the maintenance period. Non-responders received no protocol specified treatment during the 2-year observation period. Finally, participants were followed during a 5-year follow-up period. The chemotherapy regimen (CHOP or CVP or bendamustine) for individual participant was chosen by the site prior to initiation of the study.
- id
- OG001
- title
- Obinutuzumab+Chemotherapy
- param Type
- MEAN
- population Description
- The FL ITT population was defined as all randomized participants with follicular histology grouped according to their randomized treatment arm regardless of what treatments were actually received.
- reporting Status
- POSTED
- time Frame
- Baseline (Induction Cycle 1, Day 1), data cut-off (up to approximately 5 years and 2 months)
- title
- Change From Baseline in FACT-Lym Individual Subscale Lymphoma Score (Follicular Population)
- type
- SECONDARY
- unit Of Measure
- units on a scale
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Independent clinical review pending · Not medical advice