Exercise intensity and markers of inflammation during and after (neo-) adjuvant cancer treatment

in Endocrine-Related Cancer
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Tim Schauer Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

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Anne-Sophie Mazzoni Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden

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Anna Henriksson Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden

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Ingrid Demmelmaier Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden
Department of Sport Science and Physical Education, University of Agder, Kristiansand, Norway

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Sveinung Berntsen Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden
Department of Sport Science and Physical Education, University of Agder, Kristiansand, Norway

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Truls Raastad Department of Sport Science and Physical Education, University of Agder, Kristiansand, Norway
Department of Physical Performance, Norwegian School of Sport Sciences, Oslo, Norway

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Karin Nordin Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden

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Bente K Pedersen Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

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Jesper F Christensen Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

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Correspondence should be addressed to T Schauer: tim.schauer.01@regionh.dk
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Exercise training has been hypothesized to lower the inflammatory burden for patients with cancer, but the role of exercise intensity is unknown. To this end, we compared the effects of high-intensity (HI) and low-to-moderate intensity (LMI) exercise on markers of inflammation in patients with curable breast, prostate and colorectal cancer undergoing primary adjuvant cancer treatment in a secondary analysis of the Phys-Can randomized trial (NCT02473003). Sub-group analyses focused on patients with breast cancer undergoing chemotherapy. Patients performed 6 months of combined aerobic and resistance exercise on either HI or LMI during and after primary adjuvant cancer treatment. Plasma taken at baseline, immediately post-treatment and post-intervention was analyzed for levels of interleukin 1 beta (IL1B), IL6, IL8, IL10, tumor-necrosis factor alpha (TNFA) and C-reactive protein (CRP). Intention-to-treat analyses of 394 participants revealed no significant between-group differences. Regardless of exercise intensity, significant increases of IL6, IL8, IL10 and TNFA post-treatment followed by significant declines, except for IL8, until post-intervention were observed with no difference for CRP or IL1B. Subgroup analyses of 154 patients with breast cancer undergoing chemotherapy revealed that CRP (estimated mean difference (95% CI): 0.59 (0.33; 1.06); P  = 0.101) and TNFA (EMD (95% CI): 0.88 (0.77; 1); P  = 0.053) increased less with HI exercise post-treatment compared to LMI. Exploratory cytokine co-regulation analysis revealed no difference between the groups. In patients with breast cancer undergoing chemotherapy, HI exercise resulted in a lesser increase of CRP and TNFA immediately post-treatment compared to LMI, potentially protecting against chemotherapy-related inflammation.

Supplementary Materials

    • Supplementary figure 1: Correlation of IL-6 vs IL-10 during and after anti-cancer treatment. Changes of log-transformed (IL-6) vs log-transformed (IL-10) values from baseline until post-treatment in (A) intention-to-treat analysis; (B) Sub-group analysis. Values for post-treatment to post-intervention in (C) intention-to-treat analysis; (D) Sub-group analysis. Each figure panel is divided into high and low-to-moderate intensity. Method: spearman correlation
    • Supplementary table 1: Cytokine co-regulation with IL-10 throughout the intervention
    • Supplementary table 2: Baseline characteristics for subgroup analysis in breast cancer patients undergoing chemotherapy

 

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