Impact of Dose to Cardiac Substructures on Survival in Patients With Esophageal Cancer Treated With Radiotherapy or Chemoradiotherapy (SATIATION)

Sponsor
University Hospital, Brest (Other)
Overall Status
Recruiting
CT.gov ID
NCT05996276
Collaborator
(none)
150
1
2
76.1

Study Details

Study Description

Brief Summary

Treatment of non-operable esophageal cancers is based on radiochemotherapy, or exclusive radiotherapy.

The cardiac toxicity of radiotherapy in the treatment of thoracic tumor localizations is well documented, however, more and more studies are calling for the use of dosimetric parameters related to cardiac sub-structures to be integrated into clinical practice, rather than considering the heart as a whole.

With this in mind, the aim of this study is to define the parameters, particularly dosimetric ones linked to cardiac sub-structures, influencing survival in patients treated with exclusive radiotherapy or radiochemotherapy for esophageal cancer.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Treatment of non-operable esophageal cancers is based on radiochemotherapy, or exclusive radiotherapy.

    The cardiac toxicity of radiotherapy in the treatment of thoracic tumor localizations is well documented, however, more and more studies are calling for the use of dosimetric parameters related to cardiac sub-structures to be integrated into clinical practice, rather than considering the heart as a whole.

    Although most of these data have been studied in populations with long-term follow-up, such as breast cancer, cardiac toxicity and the reduced survival it entails are also found in diseases such as esophageal cancer.

    With this in mind, the aim of this study is to define the parameters, particularly dosimetric ones linked to cardiac sub-structures, influencing survival in patients treated with exclusive radiotherapy or radiochemotherapy for esophageal cancer.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    150 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Impact of Dose to Cardiac Substructures on Survival in Patients With Esophageal Cancer Treated With Radiotherapy or Chemoradiotherapy
    Actual Study Start Date :
    Aug 1, 2023
    Anticipated Primary Completion Date :
    Sep 30, 2023
    Anticipated Study Completion Date :
    Sep 30, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Overall survival (OS) [through study completion, an average of 1 year]

      OS is defined as the time elapsed between inclusion and death, whatever the cause.

    Secondary Outcome Measures

    1. The rate of cardiac events. [through study completion, an average of 1 year]

      The rate of cardiac events.

    2. Response rate. [through study completion, an average of 1 year]

      Response rate.

    3. Progression-free survival (PFS). [through study completion, an average of 1 year]

      PFS is defined as the time elapsed between inclusion and tumor progression assessed by an expert panel according to RECIST v1.1 criteria, or death from any cause.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age ≥ 18 years

    • Histologically or cytologically proven esophageal cancer

    • Localized or locally advanced esophageal cancer treated with radiochemotherapy or exclusive radiotherapy

    • Tumor dose ≥ 50 Gy

    • Non-opposition of living patients formulated

    • Patient affiliated to a social security scheme

    Exclusion Criteria:
    • Age < 18 years

    • Patient treated with upfront surgery

    • Tumor dose < 50 Gy

    • Other concomitant neoplasia

    • Metastatic patient

    • Refusal to participate

    • Patient under legal protection (guardianship, curatorship, etc...)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Chu Brest Brest France 29609

    Sponsors and Collaborators

    • University Hospital, Brest

    Investigators

    • Principal Investigator: Vincent Bourbonne, MD, PhD, Radiation Oncology Department, Brest University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Brest
    ClinicalTrials.gov Identifier:
    NCT05996276
    Other Study ID Numbers:
    • 29BRC23.0144 - SATIATION
    First Posted:
    Aug 18, 2023
    Last Update Posted:
    Aug 18, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Hospital, Brest
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 18, 2023