Physical Exercise During Preoperative Chemotherapy for Breast Cancer
Condition(s) studied
Investigational drug(s) / intervention(s)
Physical training: Participants randomized to the exercise group will complete two structured 60-min exercise sessions per week from initiation of NACT to surgery (approx. five months).
Study summary
Neoadjuvant chemotherapy (NACT) is increasingly used in breast cancer. The best proof of NACT efficacy is pathological complete response (pCR), i.e. the absence of invasive tumour on post-NACT surgical histopathology. While it is known that physical exercise can help patients to better tolerate and complete often harsh cancer treatments, it is an emerging area of research to understand if and how exercise exerts anti-tumour effects and improves oncological outcomes.
The main aim of the Neo-ACT trial is to examine if a physical exercise intervention during NACT can increase pCR rates in breast cancer. Secondary aims are residual cancer burden, radiological tumour response, patient-related outcomes (health-related quality of life, physical activity), physiological outcomes (muscle strength, cardiorespiratory fitness), cancer treatment-related toxicities (cognitive dysfunction, chemotherapy completion rates) and long-term sick leave. Furthermore, the trial will explore how physical exercise affects anti-tumoral mechanisms inherent to therapy or host by hypothesis-generating translational analyses.
712 patients with primary invasive breast cancer will be randomized to either a supervised intervention of high-intensity interval and resistance training during NACT, supported by an exercise app, or to usual care, and followed for two years. Physical activity is meticulously tracked. By offering patients active involvement, the trial contributes strongly to the concept of personalized medicine.
Eligibility
Primary outcome measure(s)
- Pathological complete response — 5-6 months
Absence of residual invasive tumor in breast and axilla at surgery
Trial sites (13)
| Facility | City | Region | Status |
|---|---|---|---|
| Cabrini Health | Melbourne | Australia | Not Yet Recruiting |
| Helsinki University Hospital | Helsinki | Finland | Recruiting |
| Turku University Hospital | Turku | Finland | Not Yet Recruiting |
| Karolinska University Hospital | Stockholm | Stockholm County | Recruiting |
| Sahlgrenska University Hospital | Gothenburg | Sweden | Recruiting |
| Skaraborgs sjukhus | Lidköping | Sweden | Recruiting |
| Capio St Görans Hospital | Stockholm | Sweden | Recruiting |
| Southern General Hospital | Stockholm | Sweden | Recruiting |
| Sundsvall Hospital | Sundsvall | Sweden | Recruiting |
| Umeå University Hospital | Umeå | Sweden | Recruiting |
| Västmanlands Hospital | Västerås | Sweden | Recruiting |
| Edinburgh Napier University | Edinburgh | Scotland | Not Yet Recruiting |
| Royal Marsden | London | United Kingdom | Not Yet Recruiting |
More Karolinska Institutet trials in Sweden
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05184582 on ClinicalTrials.gov ↗ ← All trials in Sweden