Schmidt · Journal of sport and health science 2025 · randomized controlled trial · n=180

Effects of aerobic or resistance exercise during neoadjuvant chemotherapy on tumor response and therapy completion in women with breast cancer: The randomized controlled BENEFIT trial.

Cited 16 times in the scientific literature.

Level 2 - randomized trial

Randomized controlled trial

PubMed 40447136 · doi:10.1016/j.jshs.2025.101064 · record verified 2026-08-29

What was done

In the randomized controlled BENEFIT trial, 180 women with breast cancer scheduled for neoadjuvant chemotherapy (NACT) were randomly assigned to supervised resistance training (RT, n = 60), supervised aerobic training (AT, n = 60) twice weekly during NACT, or a waitlist control group (WCG, n = 60). The primary outcome was change in tumor size (categorized due to skewed distribution). Secondary clinical outcomes derived from medical records included pathologic complete response (pCR), type of surgery, axillary lymph node dissection (ALND), premature discontinuation of chemotherapy, and relative dose intensity (RDI). Multiple (ordinal) logistic regression analyses were conducted.

What was found

There was no significant difference in post-intervention tumor size between RT or AT and WCG overall. A significant effect modification was observed by hormone receptor (HR) status (p interaction = 0.030). In HR+ tumors, AT showed trends toward improved tumor shrinkage (OR = 2.37, 95% CI: 0.97–5.78), pCR (OR = 3.21, 95% CI: 0.97–10.61), and ALND (OR = 3.76, 95% CI: 0.78–18.06) compared with WCG, with slightly less pronounced effects for RT. In HR- tumors, AT significantly improved RDI (OR = 3.71, 95% CI: 1.20–11.50), as did RT (OR = 2.58, 95% CI: 0.88–7.59). Across all participants, both exercise groups demonstrated significantly reduced premature discontinuation of chemotherapy compared with control (OR [no vs. yes] = 2.34, 95% CI: 1.10–5.06).

Why it matters

This study provides randomized trial evidence that exercise during neoadjuvant chemotherapy aids treatment adherence and completion, while offering preliminary clinical evidence that exercise may enhance tumor response in specific breast cancer subtypes.

Limits

The primary outcome was null in the overall population. Subgroup findings by hormone receptor status were derived from small subsets resulting in wide confidence intervals crossing or near the null. Skewed tumor size data necessitated categorization, which may reduce measurement granularity. Long-term recurrence and survival outcomes were not assessed in the abstract.

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