Rituximab Maintenance Therapy in Aggressive CD20 (Cluster of Differentiation Antigen 20) Positive Lymphoma and Mantle Cell Lymphoma
Primary Purpose
CD20+ Aggressive Lymphoma, Mantle Cell Lymphoma
Status
Unknown status
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
rituximab
Sponsored by
About this trial
This is an interventional treatment trial for CD20+ Aggressive Lymphoma, Mantle Cell Lymphoma focused on measuring CD20+ aggressive lymphoma, mantle cell lymphoma, rituximab, maintenance
Eligibility Criteria
Inclusion Criteria:
- aggressive B-cell lymphoma or mantle cell lymphoma
- CR (complete remission) oder CRu (complete remission unconfirmed) after previous therapy
- PR (partial remission) only when PET is negative
- minimal age 18 years
- CD20+ expression on tumor cells
- effective contraception
- Karnofsky status > 60
- written informed consent
Sites / Locations
- University of Heidelberg Hospital
- University of Mannheim Hospital
- University of Bonn Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Rituximab maintenance
Observation
Arm Description
maintenance therapy with rituximab (375 mg/m2) administered every 3 months for 2 years.
observational arm, no intervention
Outcomes
Primary Outcome Measures
Progression free survival
Primary endpoint of the study was progression free survival (PFS)
Secondary Outcome Measures
time to progression (TTP)
overall survival (OS)
response to treatment
Full Information
NCT ID
NCT01933711
First Posted
August 23, 2013
Last Updated
May 11, 2016
Sponsor
University Hospital Heidelberg
1. Study Identification
Unique Protocol Identification Number
NCT01933711
Brief Title
Rituximab Maintenance Therapy in Aggressive CD20 (Cluster of Differentiation Antigen 20) Positive Lymphoma and Mantle Cell Lymphoma
Official Title
Rituximab Maintenance Therapy Versus Observation in Aggressive CD20+ Lymphoma and Mantle Cell Lymphoma - a Prospective Randomized Phase III Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Unknown status
Study Start Date
July 2002 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Clinical and pharmacokinetic data suggest that the effect of rituximab could be improved by prolonged exposure to the drug. To test for this hypothesis we performed a prospective randomized trial of rituximab maintenance therapy versus observation in patients (pts) with aggressive CD20+ B-cell lymphoma and mantle cell lymphoma.
Detailed Description
After completion of standard treatment, pts with aggressive CD20+ B-cell lymphoma and mantle cell lymphoma were randomized to either observation or maintenance therapy with rituximab (375 mg/m2) administered every 3 months for 2 years. Both pts after first line therapy and pts after relapse treatment were included in the study. Pts with aggressive lymphoma were enrolled if they had achieved a complete response (CR) after initial treatment. Pts with aggressive lymphoma with residual tumor mass underwent positron emission tomography (PET) and qualified for randomization if this examination showed no signs of tumor activity. Pts with mantle cell lymphoma were eligible for the study if at least a partial response (PR) was achieved. Primary endpoint of the study was progression free survival (PFS), secondary endpoints were time to progression (TTP), overall survival (OS) and response to treatment. Differences between PFS and OS were analysed using the logrank test and the proportional hazard model of Cox. TTP was analyzed using a competing risk model with death as competing event.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
CD20+ Aggressive Lymphoma, Mantle Cell Lymphoma
Keywords
CD20+ aggressive lymphoma, mantle cell lymphoma, rituximab, maintenance
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
328 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Rituximab maintenance
Arm Type
Experimental
Arm Description
maintenance therapy with rituximab (375 mg/m2) administered every 3 months for 2 years.
Arm Title
Observation
Arm Type
No Intervention
Arm Description
observational arm, no intervention
Intervention Type
Drug
Intervention Name(s)
rituximab
Primary Outcome Measure Information:
Title
Progression free survival
Description
Primary endpoint of the study was progression free survival (PFS)
Time Frame
24 months after randomization
Secondary Outcome Measure Information:
Title
time to progression (TTP)
Time Frame
24 months after randomization
Title
overall survival (OS)
Time Frame
24 months after randomization
Title
response to treatment
Time Frame
24 months after randomization
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
aggressive B-cell lymphoma or mantle cell lymphoma
CR (complete remission) oder CRu (complete remission unconfirmed) after previous therapy
PR (partial remission) only when PET is negative
minimal age 18 years
CD20+ expression on tumor cells
effective contraception
Karnofsky status > 60
written informed consent
Facility Information:
Facility Name
University of Heidelberg Hospital
City
Heidelberg
State/Province
Baden-Württemberg
ZIP/Postal Code
69120
Country
Germany
Facility Name
University of Mannheim Hospital
City
Mannheim
State/Province
Baden-Württemberg
ZIP/Postal Code
68167
Country
Germany
Facility Name
University of Bonn Hospital
City
Bonn
State/Province
Nordhein-Westfalen
ZIP/Postal Code
53127
Country
Germany
12. IPD Sharing Statement
Learn more about this trial
Rituximab Maintenance Therapy in Aggressive CD20 (Cluster of Differentiation Antigen 20) Positive Lymphoma and Mantle Cell Lymphoma
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