Improving Response to Chemotherapy by Adding Physical Exercise in the Neoadjuvant Setting of Breast Cancer Patients - The KEYMOVE Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

One of the recommended treatments for breast cancer is neoadjuvant chemotherapy (NCT), however, only 20% of the patients subject to this therapy present pathologic complete response (pCR). If exercise-induced tumour size reductions observed in preclinical studies translates to humans, physical training could emerge as a way of increasing rates of pCR to NCT, which would be a valuable clinical achievement. The present randomized controlled trial primary aim is to assess the impact of a physical exercise intervention the NCT efficacy. Following a parallel-arm design, 86 women with primary BC will be allocated 1:1 to a NCT + exercise (experimental) or NCT alone (control) group. The primary outcome is the rate of pCR in each group. Secondary outcomes include treatment tolerability and compliance, tumour infiltrating lymphocytes, ki67, immune, inflammatory, matricellular and myogenic markers, physical fitness, accelerometry, quality of life and body composition.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• being female gender;

• age equals or greater than 18 years old;

• having a newly diagnosed histologically confirmed breast carcinoma IA-IIIC;

• planned to receive neoadjuvant chemotherapy with anthracyclines or taxanes, that might be associated to anti-HER2 drugs;

• being followed by the oncology department of the CHVNG/E;

• medical oncologists consents the practice of physical exercise;

• the patient is capable of providing written informed consent;

• the participant accepts to be allocated to the control or experimental group, according to the randomization.

Locations
Other Locations
Portugal
Centro Hospitalar Vila Nova Gaia e Espinho
RECRUITING
Vila Nova De Gaia
Contact Information
Primary
Nuno D Rato, MSc
nuno.rato@umaia.pt
+351 919985852
Backup
Alberto Alves, PhD
ajalves@umaia.pt
Time Frame
Start Date: 2023-07-31
Estimated Completion Date: 2026-08-01
Participants
Target number of participants: 86
Treatments
No_intervention: Control Group
The control group will receive neoadjuvant chemotherapy alone (standard of care).
Experimental: Experimental Group
The experimental group will receive neoadjuvant chemotherapy (standard of care) in conjunction with an exercise intervention. The exercise intervention will be implemented concurrently for the full duration of the neoadjuvant chemotherapy treatment.
Related Therapeutic Areas
Sponsors
Leads: University Institute of Maia
Collaborators: Associacao de Investigacao de Cuidados de Suporte em Oncologia, University of Maia, Aveiro University, Centro Hospitalar de Vila Nova de Gaia/Espinho

This content was sourced from clinicaltrials.gov