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The PARTNER trial of neoadjuvant olaparib with chemotherapy in triple-negative breast cancer

Author

Listed:
  • Jean E. Abraham

    (University of Cambridge
    University of Cambridge)

  • Karen Pinilla

    (University of Cambridge
    University of Cambridge)

  • Alimu Dayimu

    (University of Cambridge)

  • Louise Grybowicz

    (Cambridge University Hospitals NHS Foundation Trust)

  • Nikolaos Demiris

    (Athens University of Economics and Business)

  • Caron Harvey

    (Cambridge University Hospitals NHS Foundation Trust)

  • Lynsey M. Drewett

    (Royal Devon University Healthcare NHS Foundation Trust)

  • Rebecca Lucey

    (University of Cambridge
    University of Cambridge)

  • Alexander Fulton

    (University of Cambridge
    University of Cambridge)

  • Anne N. Roberts

    (Cambridge University Hospitals NHS Foundation Trust)

  • Joanna R. Worley

    (University of Cambridge
    University of Cambridge)

  • Anita Chhabra

    (Cambridge University Hospitals NHS Foundation Trust)

  • Wendi Qian

    (Cambridge University Hospitals NHS Foundation Trust)

  • Anne-Laure Vallier

    (Cambridge University Hospitals NHS Foundation Trust)

  • Richard M. Hardy

    (Cambridge University Hospitals NHS Foundation Trust)

  • Steve Chan

    (Nottingham University Hospitals NHS Trust)

  • Tamas Hickish

    (Royal Bournemouth General Hospital)

  • Devashish Tripathi

    (Royal Wolverhampton NHS Trust
    Russells Hall Hospital)

  • Ramachandran Venkitaraman

    (East Suffolk and North Essex NHS Foundation Trust)

  • Mojca Persic

    (University Hospital of Derby and Burton)

  • Shahzeena Aslam

    (Bedfordshire Hospitals NHS Foundation Trust)

  • Daniel Glassman

    (Mid Yorkshire Teaching NHS Trust)

  • Sanjay Raj

    (University Hospital Southampton NHS Foundation Trust
    Basingstoke & North Hampshire Hospital
    Royal Hampshire Hospital)

  • Annabel Borley

    (Velindre Cancer Centre)

  • Jeremy P. Braybrooke

    (University Hospitals Bristol and Weston NHS Foundation Trust)

  • Stephanie Sutherland

    (Mount Vernon Cancer Centre)

  • Emma Staples

    (Barking, Havering and Redbridge University Hospitals NHS Trust)

  • Lucy C. Scott

    (Beatson West Of Scotland Cancer Centre)

  • Mark Davies

    (Swansea Bay University Health Board)

  • Cheryl A. Palmer

    (North West Anglia NHS Foundation Trust)

  • Margaret Moody

    (West Suffolk Hospital NHS Foundation Trust)

  • Mark J. Churn

    (Worcestershire Acute Hospitals NHS Trust
    Alexandra Redditch Hospital
    Kidderminster)

  • Jacqueline C. Newby

    (Royal Free London NHS Foundation Trust)

  • Mukesh B. Mukesh

    (East Suffolk & North Essex NHS Trust)

  • Amitabha Chakrabarti

    (University Hospitals Dorset NHS Foundation Trust)

  • Rebecca R. Roylance

    (University College London Hospitals NHS Foundation Trust)

  • Philip C. Schouten

    (Cambridge University Hospitals NHS Foundation Trust)

  • Nicola C. Levitt

    (Oxford University Hospital NHS Foundation Trust)

  • Karen McAdam

    (North West Anglia NHS Foundation Trust)

  • Anne C. Armstrong

    (The Christie NHS Foundation Trust and Division of Cancer Sciences)

  • Ellen R. Copson

    (University of Southampton)

  • Emma McMurtry

    (Sale)

  • Marc Tischkowitz

    (University of Cambridge)

  • Elena Provenzano

    (Cambridge University Hospitals NHS Foundation Trust)

  • Helena M. Earl

    (University of Cambridge
    University of Cambridge)

Abstract

PARTNER is a prospective, phase II–III, randomized controlled clinical trial that recruited patients with triple-negative breast cancer1,2, who were germline BRCA1 and BRCA2 wild type3. Here we report the results of the trial. Patients (n = 559) were randomized on a 1:1 basis to receive neoadjuvant carboplatin–paclitaxel with or without 150 mg olaparib twice daily, on days 3 to 14, of each of four cycles (gap schedule olaparib, research arm) followed by three cycles of anthracycline-based chemotherapy before surgery. The primary end point was pathologic complete response (pCR)4, and secondary end points included event-free survival (EFS) and overall survival (OS)5. pCR was achieved in 51% of patients in the research arm and 52% in the control arm (P = 0.753). Estimated EFS at 36 months in the research and control arms was 80% and 79% (log-rank P > 0.9), respectively; OS was 90% and 87.2% (log-rank P = 0.8), respectively. In patients with pCR, estimated EFS at 36 months was 90%, and in those with non-pCR it was 70% (log-rank P

Suggested Citation

  • Jean E. Abraham & Karen Pinilla & Alimu Dayimu & Louise Grybowicz & Nikolaos Demiris & Caron Harvey & Lynsey M. Drewett & Rebecca Lucey & Alexander Fulton & Anne N. Roberts & Joanna R. Worley & Anita , 2024. "The PARTNER trial of neoadjuvant olaparib with chemotherapy in triple-negative breast cancer," Nature, Nature, vol. 629(8014), pages 1142-1148, May.
  • Handle: RePEc:nat:nature:v:629:y:2024:i:8014:d:10.1038_s41586-024-07384-2
    DOI: 10.1038/s41586-024-07384-2
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    Cited by:

    1. Shadi Basyuni & Laura Heskin & Andrea Degasperi & Daniella Black & Gene C. C. Koh & Lucia Chmelova & Giuseppe Rinaldi & Steven Bell & Louise Grybowicz & Greg Elgar & Yasin Memari & Pauline Robbe & Zoy, 2024. "Large-scale analysis of whole genome sequencing data from formalin-fixed paraffin-embedded cancer specimens demonstrates preservation of clinical utility," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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