Rituximab, Bortezomib,Bendamustine , Dexamethasone, Patients With Mantle Cell Lymphoma (ManteauRiBVD)
Primary Purpose
Lymphoma
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
rituximab
bortezomib
dexamethasone
Bendamustine
Sponsored by
About this trial
This is an interventional treatment trial for Lymphoma focused on measuring contiguous stage II mantle cell lymphoma, noncontiguous stage II mantle cell lymphoma, stage III mantle cell lymphoma, stage IV mantle cell lymphoma
Eligibility Criteria
DISEASE CHARACTERISTICS:
Diagnosis of mantle cell lymphoma
- Stage II-IV disease
- No neuromeningeal disease
PATIENT CHARACTERISTICS:
- WHO performance status 0-2
- No prior cancer except for carcinoma in situ of the cervix or basal cell skin cancer
- LVEF > 50%
- HIV-negative
- Hepatitis B- and C-negative
- No hepatocellular, renal, or bone marrow insufficiency unrelated to lymphoma
PRIOR CONCURRENT THERAPY:
- Not specified
Sites / Locations
- CHU de Grenoble - Hopital Michallon
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
ARM RiBVD
Arm Description
RiBVD 6 cycles every 28 days day 1 : Rituximab /Mabthera®, 375 mg/m2 en IV Bendamustine, 90 mg/m2 en IVD Bortezomib/Velcade®, 1,3 mg/m2 en IVD day 2 : - Bendamustine, 90 mg/m2 en IVD Dexamethasone, 40 mg IV day 4 : - Bortezomib/Velcade®, 1,3 mg/m2 en IVD day 8 : - Bortezomib/Velcade®, 1,3 mg/m2 en IVD day 11 : - Bortezomib/Velcade®, 1,3 mg/m2 en IVD
Outcomes
Primary Outcome Measures
Overall response rate after 4 courses of therapy
Secondary Outcome Measures
Full Information
NCT ID
NCT00740415
First Posted
August 22, 2008
Last Updated
March 15, 2016
Sponsor
French Innovative Leukemia Organisation
Collaborators
Janssen, LP, Mundipharma Pte Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT00740415
Brief Title
Rituximab, Bortezomib,Bendamustine , Dexamethasone, Patients With Mantle Cell Lymphoma
Acronym
ManteauRiBVD
Official Title
First-line Treatment of Mantle Cell Lymphoma of Old Patients . Evaluate the Efficacy, Toxicity, and Molecular Prognostic Factors of Velcade®) in Association With Chemotherapy and Immunotherapy With Rituximab
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
French Innovative Leukemia Organisation
Collaborators
Janssen, LP, Mundipharma Pte Ltd.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
RATIONALE: Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as doxorubicin, dexamethasone, and chlorambucil, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving combination chemotherapy together with rituximab and bortezomib may kill more cancer cells.
PURPOSE: This phase II trial is studying how well giving rituximab together with bortezomib, doxorubicin, dexamethasone, and chlorambucil works as first-line therapy in treating older patients with stage II, stage III, or stage IV mantle cell lymphoma.
Detailed Description
OBJECTIVES:
Primary
Evaluate the efficacy of rituximab, bortezomib, doxorubicin hydrochloride, dexamethasone, and chlorambucil as first-line therapy in patients with stage II-IV mantle cell lymphoma.
Secondary
Determine the complete response rate in these patients.
Determine the efficacy, in terms of complete and overall response, by F18 fludeoxyglucose scan.
Determine overall, disease-free, and event-free survival of these patients.
Assess tolerability of this regimen in these patients.
Evaluate the impact of factors, described in previous protocols, on response to therapy and survival.
Assess the impact of residual disease in cerebrospinal fluid on survival.
OUTLINE: This is a multicenter study.
Patients receive rituximab IV on day 1 (days 1 and 8 of the first course only); bortezomib IV on days 1, 4, 8, and 11; doxorubicin hydrochloride IV continuously over 24 hours on days 1-4; dexamethasone IV on days 1-4; and oral chlorambucil on days 20-29. Treatment repeats every 5 weeks for 4 courses in the absence of disease progression or unacceptable toxicity.
Patients who achieve at least 50% response receive 2 additional courses of therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphoma
Keywords
contiguous stage II mantle cell lymphoma, noncontiguous stage II mantle cell lymphoma, stage III mantle cell lymphoma, stage IV mantle cell lymphoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
39 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ARM RiBVD
Arm Type
Experimental
Arm Description
RiBVD 6 cycles every 28 days day 1 :
Rituximab /Mabthera®, 375 mg/m2 en IV
Bendamustine, 90 mg/m2 en IVD
Bortezomib/Velcade®, 1,3 mg/m2 en IVD day 2 : - Bendamustine, 90 mg/m2 en IVD
Dexamethasone, 40 mg IV day 4 : - Bortezomib/Velcade®, 1,3 mg/m2 en IVD day 8 : - Bortezomib/Velcade®, 1,3 mg/m2 en IVD day 11 : - Bortezomib/Velcade®, 1,3 mg/m2 en IVD
Intervention Type
Biological
Intervention Name(s)
rituximab
Other Intervention Name(s)
Mabthera ®,
Intervention Description
Rituximab, 375 mg/m2 Intraveinous
Intervention Type
Drug
Intervention Name(s)
bortezomib
Other Intervention Name(s)
Velcade
Intervention Description
-Velcade®, 1,3 mg/m2 Intraveinous on days 1, 4, 8 and 11
Intervention Type
Drug
Intervention Name(s)
dexamethasone
Intervention Description
day - Dexamethasone, 40 mg Intraveinous
Intervention Type
Drug
Intervention Name(s)
Bendamustine
Other Intervention Name(s)
Levact ®
Intervention Description
-Day 1 and day 2 Bendamustine/Levact ®,, 90 mg/m2 Intraveinous
Primary Outcome Measure Information:
Title
Overall response rate after 4 courses of therapy
Time Frame
4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS:
Diagnosis of mantle cell lymphoma
Stage II-IV disease
No neuromeningeal disease
PATIENT CHARACTERISTICS:
WHO performance status 0-2
No prior cancer except for carcinoma in situ of the cervix or basal cell skin cancer
LVEF > 50%
HIV-negative
Hepatitis B- and C-negative
No hepatocellular, renal, or bone marrow insufficiency unrelated to lymphoma
PRIOR CONCURRENT THERAPY:
Not specified
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Remy Gressin, MD
Organizational Affiliation
CHU de Grenoble - Hopital de la Tronche
Official's Role
Study Chair
Facility Information:
Facility Name
CHU de Grenoble - Hopital Michallon
City
Grenoble
ZIP/Postal Code
38043
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
http://www.filo-leucemie.org
Description
FILO website
Learn more about this trial
Rituximab, Bortezomib,Bendamustine , Dexamethasone, Patients With Mantle Cell Lymphoma
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