Hodgkin Lymphoma
Conditions
Brief summary
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.
Interventions
50mg/m2 day 1 + 15
375mg/m2 day 1 + 15
day 1 - 21
6mg/m2 day 1 + 15
Sponsors
Study design
Eligibility
Inclusion criteria
* Hodgkin Lymphoma, intermediate or advanced stage * Age \>60 and \<75 years * ECOG 2 or better * No major organ dysfunction * Ability to take aspirin or LMW Heparin
Exclusion criteria
* HL as composite lymphoma * Prior use of lenalidomide * Prior use of chemo- or radiotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dose limiting toxicities (DLT) | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall response rate (ORR) | — |
| Progression free survival (PFS) | 2 years |
Countries
Germany