C18
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Initial diagnosis of untreated colon carcinoma (NOS), UICC stage I – II, R0 (2) Treatment in the University Hospital Augsburg or in one of the partner hospitals (3) Availability of sufficient tumor material (paraffin block and/or fresh tissue) or sections (4) Written consent from the patient to participate in the study
Exclusion criteria
Exclusion criteria: (1) Neoadjuvant therapy of colon carcinoma (2) Patients unable to consent (3) Insufficient understanding of the German language (4) Patients with chronic inflammatory bowel disease (5) Patients with hereditary colorectal cancer syndromes (such as Lynch syndrome, familial adenomatous polyposis)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PFS at 36 months, stratified by MBR score, UICC and NCCN | — |
Secondary
| Measure | Time frame |
|---|---|
| (1) CSS at 60 months stratified by MBR score, UICC and NCCN. (2) Practicability of the MBR score. (3) interobserver reliability. | — |
Countries
Germany
Contacts
Universitätsklinikum Augsburg