Physical Exercise During Neoadjuvant Chemotherapy for Breast Cancer as a Means to Increase Pathological Complete Response Rates: the Randomized Neo-ACT Trial

Status: Recruiting
Location: See all (13) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• Patients with primary invasive breast cancer cT1-T3 cN0-2

• Full tumour biology available before initiation of NACT

• Oral and written consent

• Age ≥ 18 years

Locations
Other Locations
Australia
Cabrini Health
NOT_YET_RECRUITING
Melbourne
Finland
Helsinki University Hospital
RECRUITING
Helsinki
Turku University Hospital
NOT_YET_RECRUITING
Turku
Sweden
Sahlgrenska University Hospital
RECRUITING
Gothenburg
Skaraborgs sjukhus
RECRUITING
Lidköping
Capio St Görans Hospital
RECRUITING
Stockholm
Karolinska University Hospital
RECRUITING
Stockholm
Southern General Hospital
RECRUITING
Stockholm
Sundsvall Hospital
RECRUITING
Sundsvall
Umeå University Hospital
RECRUITING
Umeå
Västmanlands Hospital
RECRUITING
Västerås
United Kingdom
Edinburgh Napier University
NOT_YET_RECRUITING
Edinburgh
Royal Marsden
NOT_YET_RECRUITING
London
Contact Information
Primary
Jana de Boniface
jana.de-boniface@ki.se
+46702472305
Backup
Cecilia Haddad Ringborg
cecilia.haddad.ringborg@ki.se
Time Frame
Start Date: 2022-11-09
Estimated Completion Date: 2028-06
Participants
Target number of participants: 712
Treatments
No_intervention: Standard
Routine information on the benefit of physical activity
Experimental: Intervention
High-intensity interval and strength training during neoadjuvant chemotherapy
Related Therapeutic Areas
Sponsors
Leads: Karolinska Institutet

This content was sourced from clinicaltrials.gov