QuicDNA

  • Research type

    Research Study

  • Full title

    INTEGRATION OF LIQUID BIOPSY INTO LUNG CANCER DIAGNOSTIC PATHWAY: QuicDNA

  • IRAS ID

    328841

  • Contact name

    Magda Meissner

  • Contact email

    meissnerm1@cardiff.ac.uk

  • Sponsor organisation

    Aneurin Bevan University Health Board

  • Duration of Study in the UK

    3 years, 0 months, 1 days

  • Research summary

    Cancer genomic profiling is the mainstay of personalised cancer treatment and allows clinicians to select the most appropriate treatment for the individual patient. Clinical trials have proved that targeted therapies improves patient outcomes, including survival. It is, therefore, vital for doctors and patients to receive a genomic profile with their diagnosis as early as possible, as this will direct
    patients towards the most effective therapy.
    In the current diagnostic pathway, following GP's referral for suspicious lung cancer, genomic analysis is requested from tissue biopsy at the lung cancer multidisciplinary(MDT) meeting around 21-28 days after the first referral. Following the MDT, genomic analysis can take 14-24 days or longer if repeat biopsies are required. The current pathway is not efficient for clinicians or patients. Patients with advanced disease often deteriorate rapidly and become too unwell or die if no treatment is received and a potential treatment opportunity is lost.
    In the QuicDNA study, we propose the introduction of a non-invasive blood test for patients with high suspicion of lung cancer.
    In the QuicDNA study, a blood sample (liquid biopsy) will be collected from patients with a high suspicion of lung cancer after their GP's referral and before collection of biopsy and will be analysed in the All Wales Medical Genomics Service (AWMGS) laboratory, based at the Cardiff & Vale University Health Board in Cardiff for the detection of circulating tumour DNA (ctDNA).
    This study aims to evaluate whether ctDNA testing performed at an early stage in the lung cancer diagnostic pathway can shorten time to treatment compared to the SoC diagnostic pathway and expedite the planning of target treatment.

  • REC name

    East Midlands - Leicester Central Research Ethics Committee

  • REC reference

    23/EM/0159

  • Date of REC Opinion

    28 Jul 2023

  • REC opinion

    Further Information Favourable Opinion