A Platform Study for solId orgaN CancERs

ConditionsCancerSurgery
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16-100
SponsorUniversity of Liverpool

About this trial

Generating bespoke biosampling protocols for individual tumour specific translational projects is onerous, cumbersome and inefficient. This study aims to provide a broad platform to maximise the unique access to biopsy and resected tumour specimens available from cancer patients to provide a high-quality and efficient source of biosamples for specific translational projects. Access to historical FFPE samples and clinical data, as well as prospective fresh tissue samples, will allow interrogation of the underlying biology of these cancers. Matched pseudoanonymised clinical and radiological data will allow the development of rich high-yield datasets.

Eligibility criteria

Qualifiers

Biopsy or surgical resection as standard of care

Disqualifiers

Refusal or inability to consent, paediatric patients

Trial design

Treatments tested in this trial

  • Biosampling

Treatment groups

2,000 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Liverpool

Lead sponsor

Countess of Chester NHS Foundation Trust

Collaborator

Liverpool University Hospitals NHS Foundation Trust

Collaborator

Clatterbridge Centre for Oncology

Collaborator

Liverpool Heart and Chest Hospital NHS Foundation Trust

Collaborator

Liverpool Womens Hospital

Collaborator