This study is to evaluate the efficacy and safety of Lenalidomide plus ICE in the treatment of Refractory and Relapsed DLBCL patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
39
Shanghai Ruijin Hospital
Shanghai, Shanghai Municipality, China
Complete response rate
Time frame: 12 weeks
Progression free survival rate
Time frame: 1 year
Overall survival rate
Time frame: 1 year
Overall response rate
Time frame: 12 weeks
Safety as assessed using CTCAE v4.0
Time frame: 1 year
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