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The effects of adding zoledronic acid to neoadjuvant chemotherapy on tumour response: Exploratory evidence for direct anti-tumour activity in breast cancer

  • R E Coleman
  • , M C Winter
  • , David Cameron
  • , R. Bell
  • , D. Dodwell
  • , M. M. Keane
  • , M. Gil
  • , D. Ritchie
  • , J L Passos-Coelho
  • , D Wheatley
  • , R. Burkinshaw
  • , S J Marshall
  • , H Thorpe
  • University of Sheffield
  • University of Leeds
  • Andrew Love Cancer Centre
  • Leeds Teaching Hospitals NHS Trust
  • Galway University Hospital
  • Cell Death Regulation Group
  • Beatson West of Scotland Cancer Centre
  • Department of Head and Neck and ENT Cancer Surgery of the Portuguese Institute of Oncology of Francisco Gentil
  • Royal Cornwall Hospital

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

208 Citations (Scopus)

Abstract

Background:Pre-clinical studies have demonstrated synergistic anti-tumour effects of chemotherapy (CT) and zoledronic acid (ZOL). Within the AZURE trial, designed to determine whether the addition of ZOL to neoadjuvant therapy improves disease outcomes, a subgroup received neoadjuvant CT. We report a retrospective evaluation comparing pathological response in the primary tumour between treatment groups.Methods:In total, 205 patients received neoadjuvant CTZOL (CTZOL, n102; CT, n103). The primary end point was pathologically assessed residual invasive tumour size (RITS) at surgery. Secondary end points were pathological complete response (pCR) rate and axillary nodal involvement. Following review of surgical pathology reports (n195), outcome differences between groups were assessed adjusting for potential response modifiers.Results:Baseline characteristics and CT treatments were similar. In multivariate analysis, allowing for biological and clinical factors known to influence tumour response, the adjusted mean RITS in CT and CTZOL groups were 27.4 and 15.5 mm, respectively, giving a difference in means of 12 mm (95% confidence interval: 3.5-20.4 mm; P0.006). The pCR rate was 6.9% in the CT group and 11.7% in the CTZOL group (P0.146). There was no difference in axillary nodal involvement (P0.6315).Conclusion:These data suggest a possible direct anti-tumour effect of ZOL in combination with CT, warranting formal evaluation in prospective studies.

Original languageEnglish
Pages (from-to)1099-1105
Number of pages7
JournalBritish Journal of Cancer
Volume102
Issue number7
DOIs
Publication statusPublished - Mar 2010
Externally publishedYes

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

  • Anti-tumour activity
  • Breast cancer
  • Chemotherapy
  • Neoadjuvant
  • Pathological response
  • ZOL

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