head and neck carcinoma
Conditions
Interventions
Group 1: Oncological patients with tumors in the head and neck region for whom therapy with an immune checkpoint inhibitor (PD-1, PD-L1) is planned
Sponsors
Lehrstuhl für Hals-Nasen-Ohrenheilkunde Universität Witten/Herdecke
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Histologically confirmed head and neck carcinoma for which immune checkpoint inhibitor therapy (PD-1, PD-L1) is planned as part of treatment
Exclusion criteria
Exclusion criteria: Age under 18, lack of capacity to consent, and lack of patient consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Response to immunocheckpoint inhibitor (PD-1, PD-L) therapy, occurrence of adverse immunotherapyrelated side effects under immuno-checkpoint inhibitor (PD-1, PD-L) therapy when restaging | — |
Secondary
| Measure | Time frame |
|---|---|
| Applicability of cloud-based medical diagnostic software (BiomeOne®) in head and neck cancer. | — |
Countries
Germany
Contacts
Public ContactJonas Jae-Hyun Park
Lehrstuhl für Hals-Nasen-Ohrenheilkunde Universität Witten/Herdecke
Outcome results
None listed