This is a phase II prospective non-randomised clinical trial in newly diagnosed and previously untreated adult patients in the age range 18-60 (67) years with peripheral T-cell lymphoma. The treatment schedule will consist of three phases: induction and high-dose consolidation, followed by autologous stem cell rescue. There will be two different induction schedules: one for patients in the age range 18-60 years and one for patients aged over 60 years.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
166
CHOEP: Cyclophosphamide: 750 mg/m2 i.v. day1 Hydroxydaunorubicin: 50 mg/m2 i.v. day1 Vincristine: 1.4 mg/m2 (max 2 mg) i.v. day 1 Etoposide: 100 mg/m2 i.v. day 1-3 Prednisone: 100 mg daily p.o. day 1-5 BEAM: Carmustine: 300 mg/m2 i.v. day 1 Etoposide: 100 mg/m2 i.v. x2 daily day 2-5 Cytosine arabinoside: 200 mg/m2 i.v. x2 daily or 400 mg/m2 as continuous 24 hrs i.v. infusion, day 2-5 Melphalan: 140 mg/m2 i.v. day 6
Aarhus University Hospital
Aarhus, Denmark
Copenhagen Hospital
Copenhagen, Denmark
Vejle Hospital
Vejle, Denmark
OULO University Hospital
Oulu, Oulo, Finland
Time to treatment failure
Time frame: 5 years
Overall survival
Time frame: 5 years
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Kuopio University Hospital
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Oslo University Hospital
Oslo, Norway
Ullevaal University Hospital
Oslo, Norway
Rogaland Hospital
Rogaland, Norway
St.Olavs Hospital
Trondheim, Norway