C22.0
Conditions
Interventions
Group 1: Transarterial Chemoembolization (TACE)
Group 2: High-dose rate brachytherapy in Afterloading technique (HDRBT)
Group 3: Transarterial Chemoembolization in combination with high-dose rate brac
Sponsors
Charité Campus Virchow-Klinikum
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: non-resectable HCC with tumor board reviewed recommendation for minimally-invasive therapies including TACE and HDRBT
Exclusion criteria
Exclusion criteria: other malignancies of the liver excluding HCC
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Treatment response - measured by standardized, image morphological criteria such as (m)RECIST or LIRADS-TRA v2017at defined time points (after 2 months, after 5 months, and subsequently every 3-6 months post-intervention). | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival, Progression-free survival - measured by reporting data from the hospital's own documentation system as well as national cancer registries and, if applicable, registration offices. | — |
Countries
Germany
Outcome results
None listed