C25 C22.1 C22.0 C18
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Adults > 18 years who are able to consent to this study • Patient has consented to this study • Resectable gastrointestinal tumor such as liver cancer, colorectal cancer, cholangiocellular adenocarcinoma and pancreatic cancer • In the case of HCC and/or liver cirrhosis Child-Pugh class A or B. Only patients with Child-Pugh index class B of not more than 7 will be included • Life expectancy of 12 weeks or more
Exclusion criteria
Exclusion criteria: • Patients unable to consent • Pregnant and breastfeeding women • Tumor or tumortherapy within the last 2 years • Multiple cancers • Renal failure requiring hemo- or peritoneal dialysis. • In the case of HCC and/or liver cirrhosis Child-Pugh index class B in combination with more than slight ascites or hepatic encephalopathy > Grade I
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Area underneath the receiver operating characteristic function (AUC) of spectral features (GMFs) for discriminating blood samples of patients with confirmed liver cancer, colorectal cancer, cholangiocellular adenocarcinoma and pancreatic cancer. Spectral features are derived using laser-based infrared spectrosopy. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Proteomic profiles from mass spectrometry of blood samples of patients with confirmed liver cancer, colorectal cancer, cholangiocellular adenocarcinoma and pancreatic cancer • Routine clinical data, including medical imaging data and currently used biomarkers, of patients with confirmed liver cancer, colorectal cancer, cholangiocellular adenocarcinoma and pancreatic cancer. | — |
Countries
Germany
Contacts
Klinikum der Universität München