PSA Dynamics for Prostate Cancer Patients

  • Research type

    Research Study

  • Full title

    Personalisation of the risk-benefit ratio for prostate cancer patients undergoing radical radiotherapy

  • IRAS ID

    316790

  • Contact name

    Alan McWilliam

  • Contact email

    alan.mcwilliam@manchester.ac.uk

  • Sponsor organisation

    The University of Manchester

  • Duration of Study in the UK

    4 years, 0 months, 31 days

  • Research summary

    Prostate cancer is the most common form of cancer in men in the UK, and treatment is currently given based on risk-models that consider various tumour characteristics. These models have limited consideration for potential microscopic spread, which cannot be seen with conventional imaging. Additionally, individual biology, response to different treatment modalities, or response to radiotherapy dose over time is not considered. Consequently, patients can be over- or under-treated, and a third of patients see their cancer return, indicated by a rise in hormone prostate specific antigen (PSA), within five years.
    Our project aims to study patterns of PSA to detect cancer returning sooner than current practice. We will retrospectively analyse large cohorts of data from men with prostate cancer to improve the way that patients are selected for treatment, specifically radiotherapy, by developing better risk-models to predict whether a patient's cancer will return. PSA trajectories of prostate cancer patients will be modelled and similar trajectories grouped together and tested against outcome. Differences in trajectory between treatments (e.g., radiotherapy, surgery, systemic therapy, active surveillance), forms of recurrence, and times to recurrence will be studied.
    For patients given radiotherapy, trajectories will be linked to the radiotherapy dose distribution to see if there are any associations between dose, PSA trajectory and outcome. This will allow us to study patterns of treatment response and failure over time and develop spatially resolved anatomical risk maps. These will describe a risk function depending on an anatomical location and allow us to better understand tumour behaviour and improve personalisation of radiotherapy.
    The study will include data from patients who have multiple PSA measurements (>3) and a minimum of four years follow-up following a diagnosis of prostate cancer 2005-2019. This study involves the analysis of pseudonymised existing data only and will not require the involvement of individual participants.

  • REC name

    Yorkshire & The Humber - Bradford Leeds Research Ethics Committee

  • REC reference

    24/YH/0166

  • Date of REC Opinion

    27 Aug 2024

  • REC opinion

    Favourable Opinion