IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v583y2020i7818d10.1038_s41586-020-2481-8.html
   My bibliography  Save this article

The National Lung Matrix Trial of personalized therapy in lung cancer

Author

Listed:
  • Gary Middleton

    (University of Birmingham
    University Hospitals Birmingham NHS Foundation Trust)

  • Peter Fletcher

    (University of Birmingham)

  • Sanjay Popat

    (The Royal Marsden Hospital)

  • Joshua Savage

    (University of Birmingham)

  • Yvonne Summers

    (The Christie)

  • Alastair Greystoke

    (Newcastle University)

  • David Gilligan

    (Addenbrooke’s Hospital)

  • Judith Cave

    (Southampton University Hospitals NHS Trust)

  • Noelle O’Rourke

    (Beatson West of Scotland Cancer Centre)

  • Alison Brewster

    (Velindre Cancer Centre)

  • Elizabeth Toy

    (Royal Devon and Exeter Foundation NHS Trust)

  • James Spicer

    (Guy’s Hospital)

  • Pooja Jain

    (St James’s University Hospital)

  • Adam Dangoor

    (Bristol Haematology and Oncology Centre)

  • Melanie Mackean

    (Western General Hospital)

  • Martin Forster

    (University College Hospital)

  • Amanda Farley

    (University of Birmingham)

  • Dee Wherton

    (University of Birmingham)

  • Manita Mehmi

    (University of Birmingham)

  • Rowena Sharpe

    (University of Birmingham)

  • Tara C. Mills

    (Cancer Research UK)

  • Maria Antonietta Cerone

    (Cancer Research UK)

  • Timothy A. Yap

    (The University of Texas, MD Anderson Cancer Center)

  • Thomas B. K. Watkins

    (The Francis Crick Institute)

  • Emilia Lim

    (The Francis Crick Institute)

  • Charles Swanton

    (The Francis Crick Institute
    Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, University College London)

  • Lucinda Billingham

    (University of Birmingham)

Abstract

The majority of targeted therapies for non-small-cell lung cancer (NSCLC) are directed against oncogenic drivers that are more prevalent in patients with light exposure to tobacco smoke1–3. As this group represents around 20% of all patients with lung cancer, the discovery of stratified medicine options for tobacco-associated NSCLC is a high priority. Umbrella trials seek to streamline the investigation of genotype-based treatments by screening tumours for multiple genomic alterations and triaging patients to one of several genotype-matched therapeutic agents. Here we report the current outcomes of 19 drug–biomarker cohorts from the ongoing National Lung Matrix Trial, the largest umbrella trial in NSCLC. We use next-generation sequencing to match patients to appropriate targeted therapies on the basis of their tumour genotype. The Bayesian trial design enables outcome data from open cohorts that are still recruiting to be reported alongside data from closed cohorts. Of the 5,467 patients that were screened, 2,007 were molecularly eligible for entry into the trial, and 302 entered the trial to receive genotype-matched therapy—including 14 that re-registered to the trial for a sequential trial drug. Despite pre-clinical data supporting the drug–biomarker combinations, current evidence shows that a limited number of combinations demonstrate clinically relevant benefits, which remain concentrated in patients with lung cancers that are associated with minimal exposure to tobacco smoke.

Suggested Citation

  • Gary Middleton & Peter Fletcher & Sanjay Popat & Joshua Savage & Yvonne Summers & Alastair Greystoke & David Gilligan & Judith Cave & Noelle O’Rourke & Alison Brewster & Elizabeth Toy & James Spicer &, 2020. "The National Lung Matrix Trial of personalized therapy in lung cancer," Nature, Nature, vol. 583(7818), pages 807-812, July.
  • Handle: RePEc:nat:nature:v:583:y:2020:i:7818:d:10.1038_s41586-020-2481-8
    DOI: 10.1038/s41586-020-2481-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41586-020-2481-8
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/s41586-020-2481-8?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:583:y:2020:i:7818:d:10.1038_s41586-020-2481-8. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.