ASCENT

  • Research type

    Research Study

  • Full title

    Analysis of screen-detected lung cancers'genomic traits

  • IRAS ID

    271898

  • Contact name

    SM Janes

  • Contact email

    s.janes@ucl.ac.uk

  • Sponsor organisation

    University College London

  • Clinicaltrials.gov Identifier

    NCT04204499, ClinicalTrials.gov

  • Duration of Study in the UK

    3 years, 0 months, 2 days

  • Research summary

    The ASCENT study will explore the genetic and imaging features of lung cancers diagnosed during a lung cancer screening study (the ‘SUMMIT’ study, REC reference 17/LO/2004), that may help improve the accuracy of diagnostic techniques.

    Lung cancer screening using low-dose CT (LDCT) scans is becoming increasingly widespread, supported by evidence that such screening saves lives by diagnosing lung cancers at an early stage when treatments are more effective. However, abnormalities detected on screening CT scans include fast-growing ‘aggressive’ or slow-growing ‘indolent’ cancers as well as non-cancerous lesions, and CT alone does not identify which are which. In these cases, doctors often need to decide whether to perform an invasive test like a biopsy, or keep someone under surveillance with further CT scans.

    We plan to recruit people who are diagnosed with a lung cancer during the SUMMIT study and are referred for routine surgical treatment, with the aim of collecting a piece of the tumour and an extra blood sample at the time of their operation. We will request consent to add the data from these samples to the information being collected in the SUMMIT study, allowing us to match the samples to the previous CT scans and other medical information. Participating in ASCENT will not affect the participant's surgery or other treatments, and will not require additional visits to hospital.

    By examining the genetics of these tumours, we hope to find differences between fast- and slow-growing cancers at a very early stage. This information will then be used to develop new diagnostic tests which, in the future, would aim to reduce the risk of having biopsies or surgery for benign nodules, support the decision for surveillance in slow-growing cancers and identify which nodules are most likely to represent aggressive cancers at the earliest stage possible.

  • REC name

    South Central - Oxford A Research Ethics Committee

  • REC reference

    20/SC/0128

  • Date of REC Opinion

    18 Mar 2020

  • REC opinion

    Favourable Opinion