Patients with histologically confirmed cholangiocellular carcinoma (CCC) who underwent TARE C22.1
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Histologically confirmed cholangiocellular carcinoma (CCC) TARE performed during the specified period at University Hospital Essen Complete documentation of pre- and post-treatment CT datasets as well as clinical follow-up data
Exclusion criteria
Exclusion criteria: Incomplete documentation or missing CT data
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival (OS) from TARE Changes in body composition parameters (SI, MFI, VFI) before and after TARE | — |
Secondary
| Measure | Time frame |
|---|---|
| Association between body composition parameters and radiological response (mRECIST / RECIST 1.1) Incidence and severity of therapy-associated adverse events (CTCAE v5.0) Association of body composition changes with laboratory values and clinical parameters | — |
Countries
Germany
Contacts
Institut für Diagnostische und Interventionelle Radiologie und Neuroradiologie