# The effect of two remote exercise programs on cardiorespiratory fitness, cardiac function, and vascular health in patients with breast cancer

**Authors:** Nathan R. Weeldreyer, Charles C. Ellison, Mckenzie B. Mabalot, Cheyanne E. Helms, Zachariah B. Nealy, Zachary S. Leicht, Antonio Abbate, Christiana M. Brenin, Patrick M. Dillon, Trish Millard, Rebecca A. Krukowski, Jamie M. Zoellner, Siddhartha S. Angadi

PMC · DOI: 10.14814/phy2.70787 · Physiological Reports · 2026-02-17

## TL;DR

This study compared two remote exercise programs for breast cancer patients and found that high-intensity interval training better preserved cardiorespiratory fitness during chemotherapy.

## Contribution

The novel contribution is demonstrating that remote high-intensity interval training preserves VO2peak in breast cancer patients undergoing chemotherapy.

## Key findings

- VO2peak declined in moderate-intensity group but remained stable in high-intensity group
- NTproBNP levels increased significantly in moderate-intensity group but not in high-intensity group

## Abstract

Breast cancer is a common, survivable malignancy affecting women. With improved survival, the off‐target effects of chemotherapy, such as a decline in cardiorespiratory fitness and worse cardiovascular outcomes, have been recognized. Exercise training may help mitigate these effects. In this study, patients with breast cancer (N = 24) scheduled to undergo chemotherapy were randomized to either remotely administered high‐intensity interval training (HIIT) or moderate‐intensity exercise (MOD) based on ACSM guidelines for cancer survivors. HIIT involved three weekly sessions using the 4 × 4 protocol at 85%–90% peak heart rate (PHR), while MOD consisted of 150 min per week at 70%–75% PHR. Exercise training began 1–2 weeks before chemotherapy and continued throughout treatment. Baseline testing was conducted prior to chemotherapy and follow‐up testing 7–10 days after completion. Assessments included VO2peak, echocardiography, vascular function, and blood biomarkers. VO2peak significantly declined in MOD (n = 8; 1.50 ± 0.23 to 1.27 ± 0.28 L/min; p = 0.013, d = 1.2), while remaining stable in HIIT (n = 7; 1.58 ± 0.24 to 1.52 ± 0.28 L/min; p = 0.445, d = 0.3), with a large between‐group effect size (p = 0.109, d = 0.9). NTproBNP levels significantly increased in MOD (104.3 ± 35.1 to 158.1 ± 56.0; p = 0.018), but not in HIIT. The study was underpowered due to greater than anticipated dropout to detect significant between‐group differences in VO2peak. These data have implications for the design of scalable exercise interventions in patients undergoing chemotherapy for breast cancer.

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}
- **Diseases:** anemia (MESH:D000740), inflammation (MESH:D007249), myxedema (MESH:D009230), symptom (MESH:D012816), peripheral vascular disease (MESH:D016491), quality (MESH:D012893), hypertension (MESH:D006973), blood sugar (MESH:D006402), death (MESH:D003643), proliferative retinopathy (OMIM:603933), myocardial infarction (MESH:D009203), cardiovascular disease (MESH:D002318), diabetes (MESH:D003920), CO (MESH:D002303), retinal hemorrhage (MESH:D012166), Cancer (MESH:D009369), cytotoxicity (MESH:D064420), electrolyte abnormalities (MESH:D014883), DD (MESH:D018487), pulmonary embolus (MESH:D004617), ventricular arrhythmias (MESH:D001145), heart failure (MESH:D006333), depression (MESH:D003866), Breast cancer (MESH:D001943), tricuspid valve regurgitation (MESH:D014262), aortic stenosis (MESH:D001024), fatigue (MESH:D005221), palmo-plantar dysesthesia (MESH:D010292), myocarditis (MESH:D009205), stroke (MESH:D020521), thyrotoxicosis (MESH:C566386), New York Heart Association class IV symptoms (MESH:D006331), cardiac, vascular, and skeletal muscle toxicity (MESH:D066126), Stages I-IV (MESH:D062706), metabolic disease (MESH:D008659), MOD (MESH:D000092202), unstable angina (MESH:D000789), HIIT (MESH:D000095027)
- **Chemicals:** EDTA (-), platinum (MESH:D010984), Doxorubicin (MESH:D004317), anthracycline (MESH:D018943), Oxygen (MESH:D010100), TC (MESH:D013667), Carboplatin (MESH:D016190), AC (MESH:D000186), Pembrolizumab (MESH:C582435), Paclitaxel (MESH:D017239), Trastuzumab (MESH:D000068878), Pertuzumab (MESH:C485206), Docetaxel (MESH:D000077143), Cyclophosphamide (MESH:D003520), reactive oxygen species (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12914078/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914078/full.md

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Source: https://tomesphere.com/paper/PMC12914078