C25
Conditions
Interventions
Group 1: This is an observational study. Tumor tissue and blood are taken during routine pathological tissue analysis and routine blood draw - an thereby do not cause any additional intervention. This
Sponsors
Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: PDAC, sufficient tumor material during pathological processing available, written consent
Exclusion criteria
Exclusion criteria: tumor material too small in pathological processing, no written consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the successful establishment of a reliable patient-derived PDAC tumoroid protocol and individual chemosensitivity testing protocols | — |
Secondary
| Measure | Time frame |
|---|---|
| correlation of liquid biopsy mutation status results, tumoroid drug response and the patients' response to chemotherapeutic treatment | — |
Countries
Germany
Contacts
Public ContactChristine Nitschke
Klinik für Allgemein-, Viszeral und ThoraxchirurgieUniversitätsklinikum Hamburg-Eppendorf
Outcome results
None listed