About this trial
This study is an open, monocentric study. It includes patients with irAE refractory to standard therapy or patients where corticosteroids cannot be tapered. Patients will either be treated with ECP or second line immunosuppressive therapy according to investigator's choice. Patients will be followed for 24 weeks after first treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Subjects must we willing and able to comply with scheduled visits and must have given written informed consent.
irAE after immune checkpoint inhibitor therapy (PD-1/PD-L1 or PD-1 + CTLA4 blockade)
irAE refractory to therapy with corticosteroids or inability to taper corticosteroids to prednisone equivalent <= 5mg. An irAE is defined as refractory if corticosteroids do not improve symptoms within 72 hours. The inability to taper corticosteroids is defined as relapse on standard tapering of 1 mg/kg corticosteroid over 28 days.
Disqualifiers
Contraindications for the treatment with ECP including a known sensitivity to psoralen compounds such as 8-MOP, comorbidities that may result in photosensitivity, aphakia, history of heparin-induced thrombocytopenia, unsatisfactory cardio-circulatory function, low hematocrit values
Pregnancy
Body weight less than 40 kg.
Trial population
Patients with irAE after immune checkpoint inhibitor therapy (PD-1/PD-L1 or PD-1 + CTLA4 blockade) refractory to therapy with corticosteroids or inability to taper corticosteroids to prednisone equivalent \<= 5mg. An irAE is defined as refractory if corticosteroids do not improve symptoms within 72 hours. The inability to taper corticosteroids is defined as relapse on standard tapering of 1 mg/kg corticosteroid over 28 days.
Trial design
Cohort
Prospective
Treatments tested in this trial
Extracorporeal photopheresis
Other interventionECP consists of the three steps of leukapheresis, photoactivation and reinfusion and has immunomodulatory effects (modulation of dendritic cells, change in cytokine profile, induction of T cell subpopulations). Indications are currently the treatment of Sézary syndrome, Graft-versus-host disease (GvHD), organ transplant rejection and systemic scleroderma.
Other immunosuppressive or immunomodulatory drugs
Other interventionOther immunosuppressive or immunomodulatory drugs
Treatment groups
Trial outcomes
Primary outcomes
Immunophenotype
Characterisation of peripheral mononuclear blood cells
Secondary outcomes
Developement of grade of irAE
irAE symptoms graded according to CTCAE v5.0
Patient quality of life
Quality of life assessed by EORTC QLQ-C30
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Lucie Heinzerling
Lead sponsor
LMU Klinikum
Sponsor institution