Contribution of PET/MRI in Locally Advanced Cervical Cancer (ATICC)

Sponsor
Institut de cancérologie Strasbourg Europe (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06083103
Collaborator
(none)
50
1
27
1.9

Study Details

Study Description

Brief Summary

[18 F]fluorodeoxyglucose (18F-FDG) positron emission tomography-magnetic resonance imaging (PET/MRI) is a new hybrid imaging tool that has recently arrived in oncology, and is particularly promising. Its usefulness seems obvious in certain tumor types, but its place in the staging of cervical cancers has never been explored in a prospective trial to our knowledge.

Previously, a comparative retrospective study from 2009 found a better sensitivity of PET fused to diagnostic MRI images compared to PET/CT (positron emission tomography/computed tomography) in the detection of metastatic lymph nodes (54 and 44% respectively). It was an a posteriori fusion of images, from images acquired by PET-CT.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: 18-FDG PET-MRI

Detailed Description

This monocentric, prospective trial aims at comparing performances of 18F-FDG PET/MRI versus standard PET/CT in the detection of lymph node metastases in cervical cancer patients. Specificity and sensitivity of both exams will be compared at one timepoint, during the PET/CT prescribed in routine care for assessment of extension. PET/MRI will be conducted directly after PET/CT and a unique dose of 18F-FDG radiotracer will be used for both exams.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Contribution of PET/MRI in Locally Advanced Cervical Cancer
Anticipated Study Start Date :
Oct 2, 2023
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2025

Outcome Measures

Primary Outcome Measures

  1. Compare performances of PET/MRI and PET/CT in the detection of lumbar aortic lymph node metastases in cervical cancer patients with tumors graded IB2 to IVA stage [Up to 3 months]

    Performances in terms of sensitivity

Secondary Outcome Measures

  1. Compare performances of PET/MRI and PET/CT in the detection of lymph node metastases in cervical cancer patients with tumors graded IB2 to IVA stage, outside of lumbar aortic region [Up to 3 months]

    Performances in terms of sensitivity

  2. Compare performances PET/MRI and para-aortic lymphadenectomy in the detection of lumbar aortic lymph node metastases in cervical cancer patients [Up to 3 months]

    Lumbar/aortic lymph nodes detection with each exams

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients aged from 18 years old and over

  • Patients with presumed cervical cancer of stages IB2 to IVA based on clinical data and pelvic MRI, undergoing pre-treatment assessment.

  • For women of childbearing potential : Adequate contraception throughout study participation.

Note : enrollment in a concomitant clinical trial is authorized

Exclusion Criteria:
  • Oncological history that could possibly interfere with imaging results interpretation, apart from cervical cancer

  • Extra-nodal metastasis clinically or radiologically proven before study participation

  • Contraindication to MRI or injection of contrast agents containing gadolinium

  • Contraindication to lumbo-aortic lymphadenectomy

  • Persons deprived of liberty

  • Minor or patients placed under guardianship or supervision

  • Patient under judicial protection

  • Patient unable to consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institut de cancérologie Strasbourg Europe Strasbourg France 67033

Sponsors and Collaborators

  • Institut de cancérologie Strasbourg Europe

Investigators

  • Study Chair: Éric OUVRARD, MD, Institut de cancérologie Strasbourg Europe

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Institut de cancérologie Strasbourg Europe
ClinicalTrials.gov Identifier:
NCT06083103
Other Study ID Numbers:
  • 2021-013
  • 2023-A00743-42
First Posted:
Oct 13, 2023
Last Update Posted:
Oct 13, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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 13, 2023