Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
FEMALE
NCT06672120

Exercise in Triple- Negative Breast Cancer

Led by Technical University of Munich · Updated on 2025-05-31

120

Participants Needed

2

Research Sites

195 weeks

Total Duration

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AI-Summary

What this Trial Is About

This is a prospective, randomized, controlled mono-center study investigating the effects of a combined, supervised aerobic exercise and resistance training in female patients with newly diagnosed, therapy-naive triple-negative breast cancer (TNBC, stage I-III) between 18 and 50 years of age scheduled for anthracycline-based chemotherapy and immunotherapy with checkpoint inhibitors. All patients will receive smart watches for rhythm monitoring. Patients will be randomized (1:1) into a control group, receiving 24 weeks of standard exercise recommendations during neoadjuvant therapy, and an intervention group receiving 24 weeks of home-based, video-supervised exercise training consisting of endurance and resistance training. The primary endpoint is the change of peak oxygen consumption (VO2peak) between baseline and 24 weeks in the groups. Secondary endpoints include changes of physical function (short physical performance battery, SPPB), as well as cardiac biomarkers, quality of life, and changes of strength of the upper and lower body between baseline and 24 weeks. In addition, variables of cardiopulmonary exercise testing (CPET), resting and stress echocardiography, and burden of atrial fibrillation (AF) will be assessed. All changes in variables will be analyzed from baseline until 52 weeks as well. Both groups will receive standard exercise recommendations after 24 weeks and will be followed-up by clinical examination after 52 weeks. Echocardiographic variables (at rest and during exercise), quality of life, CPET, SPPB, strength testing, burden of AF, and cardiac biomarkers will be assessed. Changes between the end of the intervention period 24 weeks after diagnosis and the end of follow-up after 52 weeks will be analyzed. In addition, changes in variables between baseline and 52 weeks will be analyzed. As an exploratory endpoint the incidence of cancer therapy-related cardiac dysfunction (CTRCD) and immune-checkpoint inhibitor- associated myocarditis (ICI-myocarditis) will be assessed after 24 and 52 weeks.

CONDITIONS

Official Title

Exercise in Triple- Negative Breast Cancer

Who Can Participate

Age: 18Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female patients with newly diagnosed, local triple-negative breast cancer (stage I-III)
  • Age between 18 and 65 years
  • Scheduled for immunochemotherapy with pembrolizumab and anthracycline-based chemotherapy
Not Eligible

You will not qualify if you...

  • Unstable cardiac condition (such as suspected progression or unstable coronary artery disease, signs of acute heart failure, or significant arrhythmias)
  • Orthopaedic disability preventing exercise

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Preventive Sports Medicine and Sports Cardiology

Munich, Bavaria, Germany, 80992

Actively Recruiting

2

Department of Medicine, Division of Prevention and Sports Medicine TU Munich

Munich, Germany, 80809

Actively Recruiting

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Research Team

M

Martin Halle, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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