COLTEP: Interest of PET/CT at 18F-FDG in the Post-therapeutic Management of Cervical Cancer

Sponsor
University Hospital, Brest (Other)
Overall Status
Recruiting
CT.gov ID
NCT04008095
Collaborator
(none)
40
2
60
20
0.3

Study Details

Study Description

Brief Summary

A lot of studies have demonstrated the prognostic value of post therapy 18F-FDG PET/CT in the management of uterine cervical cancer. Post therapy 18F-FDG PET/CT is usually requested by a lot of clinicians.

Whereas 18F-FDG PET/CT is useful for prognosis in the follow-up, data are yet insufficient to clearly establish a formal recommendation.

This prospective multicenter observational study will evaluate the interest of post therapy 18F-FDG PET/CT in clinical management (within 2 months of treatment) in patients with cervical cancer at an advanced stage.

Main outcome :

The therapeutic impact of post therapy 18F-FDG PET/CT (within 2 months after the end of therapy) will be evaluated on the complete results included MRI.

Investigators will compare :
  • decision of clinicians without 18F-FDG PET/CT results

  • and decision of clinicians knowing entire results included results of 18F-FDG PET/CT.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    With approximately 3000 new cases estimated in France on 2017, the uterine cervical cancer is the twelfth cancer cause in women, responsible for 1000 deaths per year.

    Management of uterine cervical cancer is well defined before treatment, especially for imaging including systematically pelvic MRI and 18F-FDG PET/CT.

    A lot of studies have demonstrated the prognostic value of post therapy 18F-FDG PET/CT, due to semi quantitative parameters study, like the SUV max and delta SUV between pre and post therapy 18F-FDG PET/CT or qualitatively with the persistence of positive 18F-FDG PET/CT at the end of therapy.

    Whereas 18F-FDG PET/CT is useful for prognosis in the follow-up, data are yet insufficient to clearly establish a formal recommendation.

    Nevertheless, post therapy 18F-FDG PET/CT is still usually requested by a lot of clinicians.

    Furthermore, the group of Parisian public hospital (AP-HP) has established a guide for the management of cervical cancer (2016) and recommends to systematically realize a 18F-FDG PET/CT after treatment for advanced cervical cancer.

    Main purpose :

    Evaluate the role of post therapy 18F-FDG PET/CT in clinical management (within 2 months of treatment) in patients with uterine cervical cancer at an advanced stage.

    Main outcome :

    The therapeutic impact of post therapy 18F-FDG PET/CT (within 2 months after the end of therapy) will be evaluated on the complete results included MRI.

    Investigators will compare

    • decision of clinicians without 18F-FDG PET/CT results

    • and decision of clinicians knowing entire results included results of 18F-FDG PET/CT.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    40 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of the Interest of PET/CT at 18F-FDG in the Post-therapeutic Management of Cervical Cancer at an Advanced Stage. Multicenter Prospective Observational Study
    Actual Study Start Date :
    Jan 8, 2020
    Anticipated Primary Completion Date :
    Jan 8, 2022
    Anticipated Study Completion Date :
    Jan 8, 2025

    Outcome Measures

    Primary Outcome Measures

    1. The therapeutic impact of post therapy 18F-FDG PET/CT (within 2 months after the end of therapy) will be evaluated on the complete results included MRI. [Validated by six months follow up]

      Investigators will compare decision of clinicians without 18F-FDG PET/CT results and decision of clinicians knowing entire results included results of 18F-FDG PET/CT. Gold Standard for the diagnosis of progression will be based on the conclusions of multi-disciplinary staff ruling on the results of composite data, including clinical examination, biology, histopathology, morphological imaging (MRI), functional imaging (PET/CT) and 6-month follow-up.

    2. collection of the two décisions of RCP [Validated by six months follow up]

      To make statistical analysis possible, the collection of the two decisions will be chosen from three cases of care envisaged below: Complete therapeutic response Equivocal response: doubt about the presence of residual disease. Strong suspicion of residual disease and/or progression Then, we will collect a percentage of patients with rightly changes on management induced by the result of the PET-CT at 18F-FDG.

    Secondary Outcome Measures

    1. Physiological analysis parameter [24 months follow up]

      Diagnostic performances of PET/CT, Sensibility, Specificity, positive predictive value, negative predictive value

    2. Prognostic factors [24 months follow up]

      Especially dynamic parameters (SUV max ...) and search for a statistical correlation between this value and PFS and OS.

    3. Physiological analysis, hotspots study [24 months follow up]

      Hotspots study - Search for a density intersection between the local site residual disease of post-therapeutic 18F-FDG PET/CT and maximum-fixing tumor sites in 18F-FDG PET/CT Baseline.

    4. Physiological analysis, hotspots study [24 months follow up]

      Hotspots study - Search maximum-fixing tumor sites in 18F-FDG PET/CT Baseline

    5. Physiological analysis, hotspots study [24 months follow up]

      Assess the dosimetry of an escalation of the dose on these hotspots.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient old ≥ 18 years

    • Uterine cervical cancer with locally-advanced (FIGO 2019 IB3 to IVA)

    • Histology: squamous cell carcinoma and adenocarcinoma

    • Feasibility of a curative treatment

    • Having formulated a non-opposition

    Exclusion Criteria:
    • Minor patient < 18 years

    • Pregnancy or breastfeeding

    • Other type of tumor than squamous cell carcinoma and adenocarcinoma

    • FIGO 2019 < IB3 or > IVA

    • Non-eligibility for the examination

    • Contraindication to MRI and PET/CT

    • Previous history of cancer

    • Refusal of participation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHRU de Brest (Hôpital Morvan) Brest France 29200
    2 Centre Henri Becquerel Rouen France 76038

    Sponsors and Collaborators

    • University Hospital, Brest

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Brest
    ClinicalTrials.gov Identifier:
    NCT04008095
    Other Study ID Numbers:
    • 29BRC19.0084
    First Posted:
    Jul 5, 2019
    Last Update Posted:
    Jan 19, 2022
    Last Verified:
    Jan 1, 2022
    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 Jan 19, 2022