C22
Conditions
Interventions
Group 1: The data of the study population from the Phase II/III studies SORAMIC, SARAH and SIRVENIB form the basis for the retrospective analysis. Patients with intermediate or advanced stage hepatoce
Sponsors
Klinik und Poliklinik für Radiologie, LMU Klinikum
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients treated within the SORAMIC, SARAH and SIRVENIB study
Exclusion criteria
Exclusion criteria: Missing information regarding gender
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival (OS) based on existing patient data from treatment to death. treatment until death. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Progression-Free Survival (PFS) - Liver-specific progression-free survival (hepatic Progression-Free Survival, hPFS) - Tolerability/toxicity | — |
Countries
Germany
Contacts
Public ContactMax Seidensticker
Klinik und Poliklinik für Radiologie; LMU Klinikum
Outcome results
None listed