By the implementation of the anti-PD-1 antibody pembrolizumab and given its possible synergy with RT, the aim of the present trial is to develop a chemotherapy-free first-line treatment for patients with newly diagnosed early-stage favorable cHL.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
6 doses of 200mg Pembrolizumab iv as single agent every three weeks followed by radiotherapy 20Gy
Progression Free Survival
Time frame: PFS at 1 year
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