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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
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    Cited by:

    1. Qilin Zhang & Ziyan Xu & Rui Han & Yunzhi Wang & Zhen Ye & Jiajun Zhu & Yixin Cai & Fan Zhang & Jiangyan Zhao & Boyuan Yao & Zhaoyu Qin & Nidan Qiao & Ruofan Huang & Jinwen Feng & Yongfei Wang & Wenti, 2024. "Proteogenomic characterization of skull-base chordoma," Nature Communications, Nature, vol. 15(1), pages 1-32, December.

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