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Characterization and Kinetic of Chemotherapy-induced Cardiovascular Toxicity in Breast Cancer

Characterization and Kinetic of Chemotherapy-induced Cardiovascular Toxicity in Breast Cancer - PROTECT-COEUR

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05803889
Acronym
PROTECT-COEUR
Enrollment
2
Registered
2023-04-07
Start date
2023-09-21
Completion date
2024-02-15
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Brief summary

The combination of epirubicin-cyclophosphamide (EC) and paclitaxel (Tax) is one of the main chemotherapy treatments used in breast cancer patients. These treatments, which can be combined with anti-HER2 therapy using trastuzumab, are frequently associated with side effects including cardiac toxicity. However, this cardiac toxicity has only been demonstrated several months after treatment and using global indices such as ejection fraction. The assessment of myocardial dysfunction using regional deformations and the kinetic of this dysfunction during chemotherapy treatment has never been performed. In order to counteract these myocardial dysfunctions, it is essential to better describe the kinetic of the cardiac toxicity by initiating measurements since the beginning of the treatment, in order to be able to propose adapted countermeasures (e.g. exercise training) in parallel with the chemotherapy.

Interventions

In order to obtain information on the body composition of the patients, a body composition measurement will be performed. A resting cardiac echocardiography will be performed to record myocardial deformations in a non-vulnerable way. A non-invasive evaluation of arterial function will be performed by ultrasound on the femoral artery during a standardized passive movement of the leg. An assessment of myocardial deformations will also be performed under submaximal exercise conditions (at a target heart rate of 120 beats per minute, low to moderate exercise intensity). All of these measurements will be performed during evaluation 1 and reproduced in the same way during the 4 other sessions planned during (evaluation 2, 3 and 4) and after the treatment (evaluation 5).

Sponsors

UR 3072
CollaboratorUNKNOWN
Institut de cancérologie Strasbourg Europe
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Epirubicin-cyclophosphamide + paclitaxel group: * Female ≥ 18 years * Stage I to III breast cancer * Patient being planned for (neo)adjuvant therapy combining EC and Taxol on a weekly basis * Enrolled in a social security plan * Able to speak, read and understand French Trastuzumab group: * Female ≥ 18 years of age * Stage I to III breast cancer * Patient treated with trastuzumab * Enrolled in a social security plan * Able to speak, read and understand French

Exclusion criteria

For both groups: Epirubicin-cyclophosphamid + paclitaxel group and trastuzumab group * Implantation of a pacemaker * Contraindications to exercise * Protected adult * Psychiatric, musculoskeletal or neurological problems * Pregnant or breastfeeding woman * Uncontrolled high blood pressure * Body Mass Index \> 35 kg/m²

Design outcomes

Primary

MeasureTime frameDescription
Studying the impact of chemotherapy combining EC and Tax on myocardial deformations (at rest and at submaximal effort) in order to identify the kinetic of systolic and diastolic dysfunctions.During the treatment period, approximately 16 to 21 weeksCharacterizing the alteration of global longitudinal strain (GLS) by resting echocardiography at rest before, during, and after chemotherapy in a group of breast cancer patients receiving EC and Tax.

Secondary

MeasureTime frameDescription
Studying the kinetic of the development of vascular dysfunction in order to understand a potential vascular dysfunction that could occur during treatment with chemotherapy combining EC and Tax.During the treatment period, approximately 16 to 21 weeksAnalyze changes in myocardial deformations during submaximal exercise, vascular function assessed non-invasively by femoral artery ultrasound, and changes in the presence of markers of myocardial injury in the blood compartment.
To compare myocardial deformations (at rest and under submaximal stress) between patients treated with EC + Tax to patients treated with trastuzumab.During the treatment period, approximately 16 to 21 weeksComparison of myocardial deformations changes induced by two types of treatment: EC + Tax and Trastuzumab. For this endpoint, we will compare the end of chemotherapy treatment to the end of trastuzumab treatment.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026