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A hypoxia biomarker does not predict benefit from giving chemotherapy with radiotherapy in the BC2001 randomised controlled trial

  • Tim Smith
  • , Catharine West
  • , Nuradh Joseph
  • , Brian Lane
  • , Joely Irlam-Jones
  • , Elisabet More
  • , Hitesh Mistry
  • , Kimberley Reeves
  • , Yee Pei Song
  • , Mark Reardon
  • , Peter Hoskin
  • , Syed Hussain
  • , Helen Denley
  • , Emma Hall
  • , Nuria Porta
  • , Robert Huddart
  • , Nicholas James
  • , Ananya Choudhury
  • Manchester University
  • Sri Lanka Cancer Research
  • University of Manchester
  • The Christie NHS Foundation Trust
  • Department of Oncology and Metabolism
  • University of Sheffield
  • Shrewsbury and Telford Hospital NHS Trust
  • Institute of Cancer Research
  • Royal Marsden NHS Foundation Trust
  • Christie Hospital NHS Foundation Trust

Research output: Contribution to journalArticlepeer-review

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Abstract

BC2001 showed combining chemotherapy (5-FU + mitomycin-C) with radiotherapy improves loco-regional disease-free survival in patients with muscle-invasive bladder cancer (MIBC). We previously showed a 24-gene hypoxia-associated signature predicted benefit from hypoxia-modifying radiosensitisation in BCON and hypothesised that only patients with low hypoxia scores (HSs) would benefit from chemotherapy in BC2001. BC2001 allowed conventional (64Gy/32 fractions) or hypofractionated (55Gy/20 fractions) radiotherapy. An exploratory analysis tested an additional hypothesis that hypofractionation reduces reoxygenation and would be detrimental for patients with hypoxic tumours. RNA was extracted from pre-treatment biopsies (298 BC2001 patients), transcriptomic data generated (Affymetrix Clariom-S arrays), HSs calculated (median expression of 24-signature genes) and patients stratified as hypoxia-high or -low (cut-off: cohort median). invasive loco-regional control (ILRC); secondary overall survival. Hypoxia affected overall survival (HR = 1.30; 95% CI 0.99-1.70; p = 0.062): more uncertainty for ILRC (HR = 1.29; 95% CI 0.82-2.03; p = 0.264). Benefit from chemotherapy was similar for patients with high or low HSs, with no interaction between HS and treatment arm. High HS associated with poor ILRC following hypofractionated (n = 90, HR 1.69; 95% CI 0.99-2.89 p = 0.057) but not conventional (n = 207, HR 0.70; 95% CI 0.28-1.80, p = 0.461) radiotherapy. The finding was confirmed in an independent cohort (BCON) where hypoxia associated with a poor prognosis for patients receiving hypofractionated (n = 51; HR 14.2; 95% CI 1.7-119; p = 0.015) but not conventional (n = 24, HR 1.04; 95% CI 0.07-15.5, p = 0.978) radiotherapy. Tumour hypoxia status does not affect benefit from BC2001 chemotherapy. Hypoxia appears to affect fractionation sensitivity. Use of HSs to personalise treatment needs testing in a biomarker-stratified trial. Cancer Research UK, NIHR, MRC. [Abstract copyright: Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.]
Original languageEnglish
Article number105032
Pages (from-to)105032
Number of pages14
JournaleBioMedicine
Volume101
Early online date21 Feb 2024
DOIs
Publication statusPublished - 1 Mar 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Biomarkers
  • Disease-Free Survival
  • Dose Fractionation, Radiation
  • Humans
  • Hypoxia
  • Mitomycin
  • Treatment Outcome

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