WATCH: Atrial Fibrillation and Other Cardiac Arrhythmias and Diseases After Radiotherapy for Breast Cancer : Watch Your HeaRT

Sponsor
Sophie JACOB (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06073509
Collaborator
Clinique Pasteur Toulouse (Other), Centre Francois Baclesse (Other), Institut Curie (Other)
200
1
25
8

Study Details

Study Description

Brief Summary

The goal of this interventional study is to evaluate the risk of atrial fibrillation (AF) and other cardiac arrhythmias and diseases in breast cancer patients treated with radiation therapy (RT).

In addition to regular follow-up of patients by the radiation oncologist for 5 years, cardiovascular screening at the end of follow-up, combining the use of a connected watch and a cardiological check-up, could make it possible to identify precisely the types and frequencies of these sometimes asymptomatic, and probably underestimated, cardiac diseases.

The main questions it aims to answer are:
  • To assess the incidence of AF and other cardiac arrhythmias and diseases occurring within 5 years after RT

  • To evaluate absorbed doses in the heart and cardiac substructures (chambers, conduction nodes, coronaries, pulmonary veins) based on auto-segmentation models developped with deep learning algorithms

  • To investigate whether the risk of AF and other cardiac arrhythmias and diseases is associated with cardiac irradiation characterized by these absorbed doses (dose-response relationship)

Participants will be included between 2023 and 2025, 5 years after their RT:
  • Retrospective data collection will be based on a medical questionnaire designed to identify cardiac pathologies present prior to RT and those having occured in the past, between RT and 5 years post-RT.

  • Cross-sectional data collection will be based on screening for cardiac pathologies using a connected watch worn for 1 month (silent AF screening) and a cardiology consultation (including ECG and echocardiography) to identify cardiac pathologies at 5 years post-RT possibly not identified in the retrospective data collection.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Screening for atrial fibrillation and other cardiac arrhythmias and diseases

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
Watch Your HeaRT Study - Screening and Risk Analysis of Atrial Fibrillation and Other Cardiac Arrhythmias and Diseases After Radiotherapy for Breast Cancer
Anticipated Study Start Date :
Oct 20, 2023
Anticipated Primary Completion Date :
Oct 20, 2025
Anticipated Study Completion Date :
Nov 20, 2025

Arms and Interventions

Arm Intervention/Treatment
Breast cancer patients treated with RT 5 years ago

Retrospective and cross-sectional data collection based on a medical questionnaire and screening for atrial fibrillation and other cardiac arrhythmias and diseases.

Diagnostic Test: Screening for atrial fibrillation and other cardiac arrhythmias and diseases
In addition to retrospective data collection based on a medical questionnaire, a 5-year post-RT cardiovascular screening will include: connected smartwatches for atrial fibrillation screening complete ECG for other cardiac arrhythmias echocardiography for other cardiac diseases (including cardiac dysfunction, cardiomyopathy, valvulopathy, ...)

Outcome Measures

Primary Outcome Measures

  1. Incidence of AF [5 years]

    AF previously diagnosed between RT and RT+5 years or silent AF incidentally diagnosed at 5-year post-RT screening

Secondary Outcome Measures

  1. Incidence of non AF cardiac arrhythmia [5 years]

    non AF arrhythmia previously diagnosed between RT and RT+5 years and/or incidentally diagnosed at 5-year post-RT screening

  2. Incidence of other cardiac diseases [5 years]

    other cardiac diseases previously diagnosed between RT and RT+5 years and/or incidentally diagnosed at 5-year post-RT

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Women treated surgically for primary cancer of the left or right breast and for whom adjuvant treatment is RT with irradiation of the breast or chest wall and possibly irradiation of lymph node chains,

  • Adjuvant radiotherapy performed at Clinique Pasteur between 2018 and 2020,

  • 5-year post-RT follow-up radiation oncologist consultation performed at Clinique Pasteur

  • Age ≥ 65 years at the time of the 5-year post-RT follow-up consultation

  • Own a smartphone and able to understand and use digital tools alone and/or with the help of a caregiver ;

  • Patient having consented to connected follow-up,

  • Be affiliated to a social security scheme or equivalent

  • Be willing to participate in the study and have signed the consent form

Exclusion Criteria:
  • History of cancer before breast cancer RT

  • Recurrence of breast cancer or other cancer treated after breast cancer RT

  • History of atrial fibrillation prior to breast cancer RT

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinique Pasteur Toulouse France

Sponsors and Collaborators

  • Sophie JACOB
  • Clinique Pasteur Toulouse
  • Centre Francois Baclesse
  • Institut Curie

Investigators

  • Study Chair: Sophie Jacob, PhD, Institut de Radioprotection et de Surete Nucleaire

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sophie JACOB, Study Coordinator, Institut de Radioprotection et de Surete Nucleaire
ClinicalTrials.gov Identifier:
NCT06073509
Other Study ID Numbers:
  • WATCH_2023
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 11, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 11, 2023