Patients with CD30 positive DLBCL, primary refractory or in first relapse after R-CHOP or R-CHOP-like therapy will receive brentuximab vedotin in combination with R-DHAP, followed in responsive patients by high dose chemotherapy and ASCT.
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The rate of patients with serious toxicity during cycle 1-2 of the combination brentuximab vedotin-R-DHAP
Timeframe: 6 weeks
Metabolic CR rate (PET-diagnostic CT) after the third cycle of brentuximab vedotin-R-DHAP salvage therapy
Timeframe: 9 weeks
Rate of CTCAE grade 3/4 non-hematological toxicity, including neurotoxicity after each cycle of brentuximab vedotin-R-DHAP
Timeframe: up to 12 weeks