Actively Recruiting
PINCER Platform Study for Solid Organ Cancers to Support High Quality Translational Research
Led by University of Liverpool · Updated on 2025-08-01
2000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Liverpool
Lead Sponsor
C
Countess of Chester NHS Foundation Trust
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are conducting a platform study to collect biosamples and related data from patients with solid organ cancers. The study aims to provide an efficient and high-quality source of tumor and blood samples for specific research projects, allowing better understanding of cancer biology. It includes access to both historical tumor tissue and prospective fresh tissue samples, along with matched clinical and radiological data, to create rich datasets for translational research. Participants undergoing biopsy or surgical resection as part of their routine care may provide extra tumor tissue and blood samples. Tissue is collected either during biopsy or surgery with care to ensure pathological assessment is not compromised. Historical tumor tissue blocks may also be accessed and sampled. Blood samples can be taken up to 12 months after treatment. Samples are transported to approved facilities under material transfer agreements and used only for approved sub-studies within the platform. Participants may be asked to complete quality of life questionnaires up to 12 months after treatment. Clinical, pathological, and radiological data will be securely collected and pseudoanonymized for research. Analyses are performed in approved laboratories, and samples may be shared with academic or commercial partners. The study will monitor biosample procurement over four years, with ongoing data collection and participant involvement during this period.
CONDITIONS
Brief Title
A Platform Study for solId orgaN CancERs
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Biopsy or surgical resection as standard of care
You will not qualify if you...
- Refusal or inability to consent
- Pediatric patients
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 4 years
Participants provide tissue and blood samples collected during routine biopsy or surgery as part of standard care, as well as archived tissue samples identified from existing clinical databases.
1 visit at time of biopsy or surgery; additional visits may occur for archived tissue retrieval
Duration - Up to 12 months
Participants may provide blood samples and complete quality of life questionnaires up to 12 months following treatment.
Periodic visits for blood draws and questionnaire completion up to 12 months post-treatment
Trial Site Locations
Total: 1 location
1
University of Liverpool
Liverpool, United Kingdom, L69 3GB
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here