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High intensity exercise during breast cancer chemotherapy - effects on long-term myocardial damage and physical capacity - data from the OptiTrain RCT

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  • Additional Information
    • Publication Information:
      BMC, 2021.
    • Publication Date:
      2021
    • Collection:
      LCC:Diseases of the circulatory (Cardiovascular) system
      LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
    • Abstract:
      Abstract Background Adjuvant systemic breast cancer treatment improves disease specific outcomes, but also presents with cardiac toxicity. In this post-hoc exploratory analysis of the OptiTrain trial, the effects of exercise on cardiotoxicity were monitored by assessing fitness and biomarkers over the intervention and into survivorship. Methods; Women starting chemotherapy were randomized to 16-weeks of resistance and high-intensity interval training (RT-HIIT), moderate-intensity aerobic and high-intensity interval training (AT–HIIT), or usual care (UC). Outcome measures included plasma troponin-T (cTnT), Nt-pro-BNP and peak oxygen uptake (VO2peak), assessed at baseline, post-intervention, and at 1- and 2-years. Results For this per-protocol analysis, 88 women met criteria for inclusion. Plasma cTnT increased in all groups post-intervention. At the 1-year follow-up, Nt-pro-BNP was lower in the exercise groups compared to UC. At 2-years there was a drop in VO2peak for patients with high cTnT and Nt-pro-BNP. Fewer patients in the RT-HIIT group fulfilled biomarker risk criteria compared to UC (OR 0.200; 95% CI = 0.055–0.734). Conclusions In this cohort, high-intensity exercise was associated with lower levels of NT-proBNP 1-year post-baseline, but not with cTnT directly after treatment completion. This may, together with the preserved VO2peak in patients with low levels of biomarkers, indicate a long-term cardioprotective effect of exercise. Trial registration Clinicaltrials. govNCT02522260 , Registered 13th of august 2015 – Retrospectively Registered Graphical abstract
    • File Description:
      electronic resource
    • ISSN:
      2057-3804
    • Relation:
      https://doaj.org/toc/2057-3804
    • Accession Number:
      10.1186/s40959-021-00091-1
    • Accession Number:
      edsdoj.1c7be6fd961430cb115dc6b74005c9f