Avoiding Cardiac Toxicity in Lung Cancer Patients

  • Research type

    Research Study

  • Full title

    Avoiding Cardiac Toxicity in lung cancer patients treated with curative-intent radiotherapy to improve survival

  • IRAS ID

    216324

  • Contact name

    Kevin Franks

  • Contact email

    kevin.franks@nhs.net

  • Sponsor organisation

    The Leeds Teaching Hospitals NHS Trust

  • Duration of Study in the UK

    2 years, 4 months, 30 days

  • Research summary

    Radiotherapy plays a major role in the treatment of lung cancer and recent advances have improved cure rates. However, the dose needed to destroy the cancer cells can unfortunately also damage the surrounding organs, such as the heart. The precise mechanism of damage and which area of the heart is more sensitive to radiation is not currently known. This project uses the analysis of large amounts of existing radiotherapy data to determine this. Establishing detailed radiotherapy dose limits for the heart will lead to the delivery of heart-sparing radiotherapy, where possible, in lung cancer patients treated in Yorkshire and Greater Manchester. For these patients we think this will improve one-year survival by approximately 10%.
    The overall project comprises seven ‘work packages’ (WP), of which this study makes up the foundation work and are called ‘WPs 1&2’.
    WP1 will focus on the data mining validation:
    *Validation of the correlation found between the dose of radiotherapy given to the heart and the subsequent mortality of these patients.
    *Data from Manchester lung cancer patients treated with curative radiotherapy will be validated using data from patients in Leeds. The cohort in Leeds will have been treated with either standard curative radiotherapy or SABR which will allow cardiac toxicity to be modelled in greater detail.
    WP2 - collection and analysis of retrospective cardiac risk factors:
    *Radiotherapy planning CT scans will be analysed to quantify any coronary artery calcification .The calcification severity will be correlated with survival and other cardiac risk factors.
    *We will identify and record clinical risk factors to ascertain the pre-RT heart disease risks. For each patient we will obtain information on current and previous medical history, smoking status, current medications and calculate their Qrisk®3 score from the electronic patient record (EPR).
    *We will also Identify the cause of death from the (EPR) and link this to the NCRAS dataset.

  • REC name

    Yorkshire & The Humber - Leeds East Research Ethics Committee

  • REC reference

    18/YH/0058

  • Date of REC Opinion

    16 Mar 2018

  • REC opinion

    Favourable Opinion