Skip to main content
Clinical Trials/NCT06522971
NCT06522971
Active, not recruiting
Not Applicable

Exploration of the Molecular Mechanisms Behind the Effects of Physical Exercise on Response to Neoadjuvant Chemotherapy in Breast Cancer Patients

Latvian Biomedical Research and Study Centre1 site in 1 country55 target enrollmentAugust 16, 2022
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Latvian Biomedical Research and Study Centre
Enrollment
55
Locations
1
Primary Endpoint
Miller-Payne grade
Status
Active, not recruiting
Last Updated
7 months ago

Overview

Brief Summary

The goal of this clinical trial is to learn how regular physical exercise affects breast cancer patients' response to standard neoadjuvant chemotherapy (NAC) and to gain an insight into the molecular mechanisms underlying the effects of exercise on cancer biology. of exercise-induced alterations in cancer gene expression and the immune tumor microenvironment. The main questions it aims to answer are:

  • Does a high-intensity interval training (HIIT) program during treatment improve patients' response to NAC and quality of life as compared to low level of physical activity during the treatment?
  • What are the differences in the residual tumor gene expression and tumor infiltrating immune cell profile between patients taking HIIT during the NAC and patients with low level of physical activity?
  • What are the roles of extracellular vesicles (EVs) in mediating the effects of exercise on cancer progression?

Patients in HIIT group will undergo a personalized HIIT program consisting of 3 training sessions per week for the whole duration of NAC, whereas patients from the control group (Ctrl) will be advised to maintain their usual level of physical activity during NAC. After the breast surgery, response to NAC will be assessed by Miller-Payne grading. Tumor and normal breast tissue specimens will be collected for RNA sequencing analysis. Blood samples will be collected before and immediately after the training for the analysis of RNA and protein cargo of circulating EVs.

Registry
clinicaltrials.gov
Start Date
August 16, 2022
End Date
December 30, 2027
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Miller-Payne grade

Time Frame: 6 months

Response to NAC assessed by histological examination of residual tumor at surgery using Miller-Payne grading from 1 to 5, where grade 1 means no response or some alterations to individual malignant cells but no reduction in overall cellularity, whereas grade 5 is a pathological complete response.

Gene expression profile

Time Frame: 12 months

Alterations in the tumor gene expression profile will be assessed by RNA sequencing of surgical tumor and normal breast tissue specimens

Secondary Outcomes

  • Protein cargo of extracellular vesicles(Before intervention and after 6 months)
  • Breast cancer-related quality of life(6 months)
  • 30 sec sit-to-stand test(Before intervention and after 6 months)
  • 6-minute walk test(Before intervention and after 6 months)
  • Number and phenotype of tumor-infiltrating immune cells(12 months)
  • Global health-related quality of life(6 months)
  • VO2 peak(Before intervention and after 6 months)
  • RNA cargo of extracellular vesicles(Before intervention and after 6 months)

Study Sites (1)

Loading locations...

Similar Trials