Pembrolizumab in First-Line Treatment of Advanced-Stage Classical Hodgkin Lymphoma
- Registration Number
- NCT06045195
- Lead Sponsor
- University of Cologne
- Brief Summary
The primary objective of this trial is to estimate efficacy of the novel regimen. The primary endpoint is the 1-year PFS rate after treatment with one dose of pembrolizumab followed by four to six cycles of chemo-immunotherapy with P-BrECADD, and PET-guided radiotherapy as per standard of care
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
- age 18-60
- advanced stage classical Hodgkin Lymphoma
- no previous treatment for cHL
Main
Exclusion Criteria
- Nodular lymphocyte-predominant Hodgkin lymphoma or composite lymphoma
- Chemotherapy or radiotherapy in medical history
- Prior or concurrent disease that prevents treatment according to protocol
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Treatment Pembrolizumab Pembrolizumab + BrECADD
- Primary Outcome Measures
Name Time Method progression free survival 1 year
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
1st Department of Medicine, Cologne University Hospital
🇩🇪Cologne, Germany