Primary objective of the trial is to demonstrate non-inferior efficacy of six cycles of BrECADD compared to six cycles of escalated BEACOPP, each followed by radiotherapy to PET-positive residual lesions ≥2.5 cm, in terms of progression free survival (efficacy objective).
If non-inferior efficacy can be shown, the co-primary objective is to further demonstrate reduced toxicity of the BrECADD treatment compared to the escalated BEACOPP treatment measured by treatment related morbidity (TRMorbidity objective).
Condition | Classical Hodgkin Lymphoma |
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Treatment | cyclophosphamide, etoposide, prednisone, Dexamethasone, Bleomycin, vincristine, doxorubicin, dacarbazine, procarbazine, brentuximab vedotin |
Clinical Study Identifier | NCT02661503 |
Sponsor | University of Cologne |
Last Modified on | 11 August 2022 |
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