The purpose of this study is to determine the selected dose of aflibercept when it is combined with R-CHOP treatment (Rituximab/Cyclophosphamide/Doxorubicin/Vincristine/Prednisone +/- intrathecal Methotrexate) administered every 2 weeks or every 3 weeks, in non Hodgkin B-cell lymphoma, and to determine how the body handles aflibercept when it is administered with R-CHOP.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
25
in combination with standard treatment R-CHOP
Sanofi-Aventis Administrative Office
Paris, France
selected dose of aflibercept based on Dose Limiting Toxicities observed
Time frame: cycle 1 +/- 2
Adverse events
Time frame: treatment period
Response rate
Time frame: cycle 2, 4 and 8
Progression free survival
Time frame: study period
Biomarkers
Time frame: Study period
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