Improving Radiotherapy in PROState Cancer Using EleCtronic Population-based healthCAre Data: The PROSECCA Study, Answering New Questions in Prostate Cancer

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Nearly half of all cancer patients receive radiotherapy as part of their treatment and although it is effective at destroying cancerous lesions deep within the body, this comes at the cost of damaging healthy, or normal, tissues. With 50% of cancer patients surviving for 10 years or more, these patients can be left with life-changing side effects from their radiotherapy. It is clear that more must be done to limit damage to normal healthy tissue without compromising annihilation of the tumour and curing patients. The key to this is personalising an individual's radiotherapy treatment, in other words rather than assuming that all tumours respond similarly to radiotherapy, the treatment is optimised for an individual. To date, approaches to do this have been restricted to small numbers of carefully selected patients, are inordinately expensive, and not suitable for rolling out into everyday practice across the NHS. There is however another way, namely using Artificial Intelligence (AI) combined with an individual's healthcare record. By linking together large numbers of healthcare records at a national level, combined with the power of AI, the PROSECCA project will transform radiotherapy and cancer care.

Eligibility
Participation Requirements
Sex: Male
Healthy Volunteers: f
View:

• External beam radiotherapy delivered by a linear accelerator

• Prostate Specific Antigen (PSA) recorded at regular intervals after radiotherapy

• Minimum of 10 year survival post-radiotherapy

• Diagnostic Computerised Tomography (CT) acquired

• Radiotherapy planning CT acquired

• Radiotherapy treatment planning data available

• Corresponding healthcare data available to infer toxicity events (ref previous work by Lemanska et al)

Locations
Other Locations
United Kingdom
University of Edinburgh
RECRUITING
Edinburgh
Contact Information
Primary
Bill Nailon
w.nailon@ed.ac.uk
0044 1315371000
Backup
Duncan McLaren
Duncan.McLaren@ed.ac.uk
0044 1316518706
Time Frame
Start Date: 2024-07-01
Estimated Completion Date: 2028-09-30
Participants
Target number of participants: 15000
Related Therapeutic Areas
Sponsors
Collaborators: Public Health Scotland, Movember Foundation, NHS Grampian, NHS Research Scotland, NHS Greater Glasgow and Clyde, University of Lyon, Prostate Cancer UK, University of Glasgow, NHS Lothian, NHS Highland, NHS Tayside
Leads: University of Edinburgh

This content was sourced from clinicaltrials.gov