The purpose of this study is to determine within the scope of the trial what the maximum tolerated dose (MTD) of lenalidomide in combination with AVD should be.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
1st Dept. of Medicine, Cologne University Hospital
Cologne, North Rhine-Westphalia, Germany
Dose limiting toxicities (DLT)
Overall response rate (ORR)
Progression free survival (PFS)
Time frame: 2 years
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6mg/m2 day 1 + 15