C15 C16 C22 C23 C24 C25
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with GI- and HPB-CA
Exclusion criteria
Exclusion criteria: Patients with poor condition who cannot tolerate chemotherapy and targeted therapy. Patients with impaired organ functions, heart failure (New York Heart Association III-IV), coronary heart disease, myocardial infarction within 6 months, severe cardiac arrhythmia and respiratory failure. Patients diagnosed with other cancer within 5 years. Patients who are pregnant or breastfeeding. Patients enrolled in other clinical trials or incompliant of regular follow up. Patients who did not provide an informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CTC counts at several timepoints, before/after endoscopy, before/after neoadjuvant therapy and before/after surgery as well as following up after 3 and 6 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of apoptotic response and infiltration with immune cells in response to standard and immunotherapeutic regimens in tumour organoid cultures of GI-CA and HPB-CA | — |
Countries
Germany
Contacts
Universitätsklinik für Allgemein- und Viszeralchirurgie, Klinikum Oldenburg