Comparison DW-MRI vs FDG PET/CT in the Detection of Early Recurrence of Cervical Well-differentiated Thyroid Carcinoma (THYRIRMTEP)

Centre Henri Becquerel

Status and phase: Completed; Phase 2

Conditions: Relapse; Thyroid Cancer

Treatments: Device: MRI imaging; Device: PET

Study type: Interventional

Funder types: Other

Identifiers

NCT02515084

CHB 10-03

Details and patient eligibility

About

The purpose of the study is to evaluate the concordance between the 18F-PET/CT under thyrotropin stimulation and the diffusion-weighted Magnetic Resonance Imaging, in the detection of residual mass in 40 patients with partial response or relapsed differentiated thyroid carcinoma.

Full description

The schedule and the procedures of the study are the following ones :

• Baseline evaluation :

  • Clinical examination with neck echography after rhTSH stimulation
  • Normal whole body scan

• First visit (inclusion):

  18F-FDG PET/CT DW-MRI of the neck if possible performed shortly after the PET CT or within following days

• Following visits: at 6 months and 12 months

  • DW-MRI of the neck performed shortly after the PET CT or within following days.
  • Ultrasonography guided fine needle aspiration for cytology for detection of cervical metastases and identifying thyroglobuline in the needle washout fluid if needed and in case of positivity of either PET or DW-MRI exams.
  • Histological assessment of biopsies if performed

Enrollment: 37 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or female,

• Subjects must be 18 years of age or older,

• Histologically confirmed papillary or follicular differentiated thyroid carcinoma with partial response or complete response, defined by

  • Thyroglobulin > 2 μg/L under thyrotrophin stimulation, four months after at least two 131-I based treatments (3,7 GBq/100mCi or more if optimal conditions),
  • Negative extension assessment (total body bone scan, (3,7 GBq/100 mCi or more)), echography, CT scan ( neck, thorax, abdomen): no findings..

• Patient's Informed Consent form signed.

Exclusion criteria

• History of previous cancer within the least three years,
• Performance Status > 2,
• Protected adults
• Any medical, psychological, social or disabling conditions that could interfere or jeopardize the patient's participation
• History of allergy to radio-iodine,
• Estimated GFR < 45 ml/min /m² (MDRD method),
• Women of childbearing potential without contraceptive method,
• Uncontrolled diabetes mellitus,
• Hypersensitivity to FDG or to any radio-tracers,
• Contraindication to administration of Thyrogen® 0.9mg
• Intraocular foreign bodies or any metallic foreign bodies that contraindicates the MRI.
• Vascular clips, any object or implanted device that could interact with the ferromagnetic field,
• Coronary and peripheral clips, aortic stent grafts, prosthetic heart valves, annuloplasty rings, vena cava filters, cardiac pacemaker, implantable cardiovascular defibrillators....,
• Implanted insulin infuser
• Neurostimulator device
• Claustrophobia
• Agitation or psychological trouble

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

37 participants in 1 patient group

18F-FDG-PET and dw-MRI

Experimental group

Description:

At the inclusion, both all patients, a 18F-FDG-PET/CT and a dw-MRI will be performed

Treatment:

Device: PET

Device: MRI imaging