C19 C78
Conditions
Interventions
Group 1: As this is an observational study only there are no additional risks for the patient. The treatment is chosen individually for the patient and takes place independently of the study presented
Sponsors
LMU München
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: • Histologically proven mCRC • Patients with liver dominant metastatic CRC • Inclusion after full resection or local ablation of liver metastases • ECOG 0-2 • Limited extrahepatic metastases
Exclusion criteria
Exclusion criteria: • Life expectancy =3 months • Known liver cirrhosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Biomarker development (ctDNA) after local therapy or locoregional therapy regimen. | — |
Secondary
| Measure | Time frame |
|---|---|
| Progression free survival as determined by HBI MRI of the liver and CT Thorax & Abdomen | — |
Countries
Germany
Contacts
Public ContactJens Ricke
LMU München Klinik und Poliklinik für Radiologie
Outcome results
None listed