About this trial
EVIDENT's aim is to test if ex vivo drug screening can predict whether patients with solid cancers will respond, or not respond, to standard care treatments. Patients undergoing standard care surgery to excise their tumour, those undergoing a biopsy, or those having a fluid aspirate of a solid tumour with surplus tissue available after diagnostic use will be eligible for this study. The specimen will then be assessed with ex vivo drug screening utilising all standard therapies and therapies that are more novel and in early stages of development. The results of the ex vivo drug screen will be compared to the cancer's actual response to standard care treatments for those that undergo therapy to determine how effective the test is at predicting treatment response.
Eligibility criteria
Qualifiers
Present with a recurrence of a previously treated tumour. This may be a local or metastatic recurrence
Have undergone treatment for their cancer, but fail to respond to this and progress
Have received neoadjuvant therapy for their tumour
Have undergone chemotherapy, targeted therapy, immunotherapy, hormone therapy and or radiotherapy for a previous tumour
Disqualifiers
None
Trial design
Treatments tested in this trial
- Functional drug screen
Treatment groups
6
Treatment groupsSee each treatment group below.
Sponsors and collaborators
Sheffield Teaching Hospitals NHS Foundation Trust
Lead sponsor
University of Sheffield
Collaborator