Safety and Efficacy of Fludarabine and Cyclophosphamide + Rituximab
Primary Purpose
Follicular Lymphoma
Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
rituximab
rituximab,fludarabine, cyclophosphamide
Sponsored by
About this trial
This is an interventional treatment trial for Follicular Lymphoma focused on measuring follicular lymphoma, non-Hodgkin lymphoma, Fludarabine, Cyclophosphamide, Rituximab, combination, immuno-chemotherapy, relapsed
Eligibility Criteria
Inclusion Criteria:
- histologically documented WHO grade 1-2 ,CD20+,follicular lymphoma
- relapsed Follicular lymphoma
- stage III or IV disease
- Stage II patients are eligible if they present with B symptoms or bulky disease
- to have a need for therapy in the opinion of treating clinician
- measurable disease
- expected survival of 6 months or more
- age 18 to 70 years
- to have undergone < 3 lines of chemotherapy
- performance status of 0 to 2
Exclusion Criteria:
- known HIV infections
- Known Hepatitis B or C
- CNS lymphoma
- previous malignancies, or cardiac, renal, hepatic, or respiratory failure
- Pregnant or lactating women and patients of child bearing potential unless using birth control measures
Sites / Locations
- Ospedale di Arezzo
- Ospedale Maggiore di Milano
- Ospedale Monteluce
- Ospedale di Pescara
- Ospedale di Piacenza
- Ospedale di Pisa
- Ospedale di Reggio Calabria
- Ospedale S. Maria Nuova
- Ospedale Molinette
Outcomes
Primary Outcome Measures
Toxicity during the treatment period
Efficacy evaluated in terms of complete and partial response 1 month after the end of therapy
Secondary Outcome Measures
Efficacy evaluated in terms of molecular response ( bone marrow Bcl2 negativity after treatment)
Full Information
NCT ID
NCT00393107
First Posted
October 25, 2006
Last Updated
October 25, 2006
Sponsor
Gruppo Italiano Studio Linfomi
1. Study Identification
Unique Protocol Identification Number
NCT00393107
Brief Title
Safety and Efficacy of Fludarabine and Cyclophosphamide + Rituximab
Official Title
Phase II Study of Rituximab in Combination With Fludarabine and Cyclophosphamide for the Treatment of Relapsed Follicular Lymphoma
Study Type
Interventional
2. Study Status
Record Verification Date
October 2006
Overall Recruitment Status
Completed
Study Start Date
March 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Gruppo Italiano Studio Linfomi
4. Oversight
5. Study Description
Brief Summary
Purpose of this study was to assess the safety profile and the anti-lymphoma activity of the FC+R combination.
Detailed Description
The natural history of follicular lymphomas is characterized by a high initial response rate to chemotherapy followed invariably by relapse, with subsequent remissions of progressively shorter duration. The majority of patients eventually die of their disease. As yet, there is no gold standard for the treatment of newly diagnosed or relapsed advanced FL.Rituximab(R) has been shown to be a highly effective agent in the treatment of FL, either alone or in combination with chemotherapy. The ability of R to sensitize indolent lymphoma derived cell lines to cytotoxic chemotherapy agents has been demonstrated. Furthermore, fludarabine (F) may also sensitize cells to the effects of R. Cyclophosphamide (C) and F have shown in vivo synergistic activity. In view of the single agent activity and demonstrated synergy between C and F, and between F and R, we evaluated FC+R in previously treated patients with advanced FL. The primary aim of this study was to assess the safety profile and clinical activity of the FC+R combination. The secondary goal was to evaluate the ability of the treatment to convert bone marrow Bcl2 positivity such that patients achieved molecular remissions.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Follicular Lymphoma
Keywords
follicular lymphoma, non-Hodgkin lymphoma, Fludarabine, Cyclophosphamide, Rituximab, combination, immuno-chemotherapy, relapsed
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
54 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
rituximab
Intervention Type
Drug
Intervention Name(s)
rituximab,fludarabine, cyclophosphamide
Primary Outcome Measure Information:
Title
Toxicity during the treatment period
Title
Efficacy evaluated in terms of complete and partial response 1 month after the end of therapy
Secondary Outcome Measure Information:
Title
Efficacy evaluated in terms of molecular response ( bone marrow Bcl2 negativity after treatment)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
histologically documented WHO grade 1-2 ,CD20+,follicular lymphoma
relapsed Follicular lymphoma
stage III or IV disease
Stage II patients are eligible if they present with B symptoms or bulky disease
to have a need for therapy in the opinion of treating clinician
measurable disease
expected survival of 6 months or more
age 18 to 70 years
to have undergone < 3 lines of chemotherapy
performance status of 0 to 2
Exclusion Criteria:
known HIV infections
Known Hepatitis B or C
CNS lymphoma
previous malignancies, or cardiac, renal, hepatic, or respiratory failure
Pregnant or lactating women and patients of child bearing potential unless using birth control measures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sacchi Stefano, MD
Organizational Affiliation
GISL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ospedale di Arezzo
City
Arezzo
ZIP/Postal Code
52100
Country
Italy
Facility Name
Ospedale Maggiore di Milano
City
Milano
ZIP/Postal Code
20100
Country
Italy
Facility Name
Ospedale Monteluce
City
Perugia
ZIP/Postal Code
06110
Country
Italy
Facility Name
Ospedale di Pescara
City
Pescara
ZIP/Postal Code
89100
Country
Italy
Facility Name
Ospedale di Piacenza
City
Piacenza
ZIP/Postal Code
29100
Country
Italy
Facility Name
Ospedale di Pisa
City
Pisa
ZIP/Postal Code
56100
Country
Italy
Facility Name
Ospedale di Reggio Calabria
City
Reggio Calabria
ZIP/Postal Code
89100
Country
Italy
Facility Name
Ospedale S. Maria Nuova
City
Reggio Emilia
ZIP/Postal Code
42100
Country
Italy
Facility Name
Ospedale Molinette
City
Torino
ZIP/Postal Code
10100
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
11431352
Citation
Alas S, Bonavida B. Rituximab inactivates signal transducer and activation of transcription 3 (STAT3) activity in B-non-Hodgkin's lymphoma through inhibition of the interleukin 10 autocrine/paracrine loop and results in down-regulation of Bcl-2 and sensitization to cytotoxic drugs. Cancer Res. 2001 Jul 1;61(13):5137-44.
Results Reference
background
PubMed Identifier
11297268
Citation
Alas S, Emmanouilides C, Bonavida B. Inhibition of interleukin 10 by rituximab results in down-regulation of bcl-2 and sensitization of B-cell non-Hodgkin's lymphoma to apoptosis. Clin Cancer Res. 2001 Mar;7(3):709-23.
Results Reference
background
PubMed Identifier
11564066
Citation
Di Gaetano N, Xiao Y, Erba E, Bassan R, Rambaldi A, Golay J, Introna M. Synergism between fludarabine and rituximab revealed in a follicular lymphoma cell line resistant to the cytotoxic activity of either drug alone. Br J Haematol. 2001 Sep;114(4):800-9. doi: 10.1046/j.1365-2141.2001.03014.x.
Results Reference
background
PubMed Identifier
10515887
Citation
Bellosillo B, Villamor N, Colomer D, Pons G, Montserrat E, Gil J. In vitro evaluation of fludarabine in combination with cyclophosphamide and/or mitoxantrone in B-cell chronic lymphocytic leukemia. Blood. 1999 Oct 15;94(8):2836-43.
Results Reference
background
Citation
Sacchi S., Tucci A, Merli F, Orsucci L, Cervetti G, Occhini U, Liberati M, Tarantini G, Callea V, Brugiatelli M, Lauta VM, Baldini L, Luminari S, Federico M. Dipartimento di Oncologia ed Ematologia,. Phase II Study with Fludarabine and Cyclophosphamide Plus Rituximab (FC+R) in Relapsed Follicular Lymphoma Patients. ASH 2002. Blood 99, 2002 Ab n° 530
Results Reference
background
Links:
URL
http://www.gisl.org
Description
Related Info
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Safety and Efficacy of Fludarabine and Cyclophosphamide + Rituximab
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