Overview
HD11 for Intermediate Stages
Status:
Completed
Completed
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
This study is designed to (1) compare the efficacy of the BEACOPP regimen with that of ABVD as a 4-cycle chemotherapy combined with an involved field irradiation and (2) to define the optimum radiation dose comparing of 30 to 20 Gy in the same context.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University of CologneTreatments:
Bleomycin
Doxorubicin
Etoposide
Liposomal doxorubicin
Prednisone
Procarbazine
Vinblastine
Vincristine
Criteria
Inclusion Criteria:- Hodgkin´s lymphoma (histologically proven)
- CS (PS) IA, IB, IIA, with one of the risk factors a-d CS (PS) IIB only with risk
factor c or d
1. bulky mediastinal mass (> 1/3 maximum transverse thorax diameter)
2. extranodal involvement
3. ESR > 50 (A), > 30 (B-symptoms)
4. 3 or more lymph node areas involved
- written informaed consent
Exclusion Criteria:
- Leukocytes <3000/microl
- Platelets <100000/microl
- Hodgkin´s Disease as "composite lymphoma"
- Activity index (WHO) < grade 2