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Status unknownNCT03402425BUFUpdated Mar 28, 2019

The Diagnostic Value of 18F-FET PET/MRI for CNS Tumors in Children and Adolescents

An interventional study of 18F-FET PET in Positron-Emission Tomography and Brain Neoplasms, Childhood, sponsored by Rigshospitalet, Denmark. Status unknown at 1 site in Denmark. Per ClinicalTrials.gov, last updated 2019-03-28.

Sponsored by Rigshospitalet, Denmark · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Mar 2019), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Not applicable
Sex
All
01

Study summary

To investigate the diagnostic value of 18F-FET PET/MRI instead of MRI alone, children and adolescents with tumor in brain or spinal cord are included and scanned primarily at our hybrid PET/MRI using the amino acid analog 18F-FET. The scans are performed at primary diagnosis, before radiation therapy, before and after operation, when relapse is suspected and three or six months after initiation of chemotherapy.

Read the detailed description

Background. Tumors in the brain and spinal cord are among the most common causes of death and disability by cancer in children and adolescents. MRI is used for primary diagnosis as well as follow-up but is often challenged by tissue changes caused by the treatment. The amino acid analog 18F-FET is used increasingly in adults to delineate tumor and discriminate tumor from treatment effects. A hybrid PET/MRI scanner enables the simultaneous imaging with PET and MRI, which is important in especially the younger children needing anaesthesia to cooperate to the procedure.

Aim The aim of the study is to compare diagnostics using MRI alone with 18F-FET PET/MRI (or sequential MRI and PET) in children and adolescents diagnosed with a central nervous system (CNS) tumor before the age of 18 years. The scans will be performed at primary diagnosis/before operation/biopsy, within 72 hours after operation, planning radiation therapy, evaluation of treatment effect, when relapse is suspected.

Exclusion criteria are MRI contraindications, pregnancy, or a syndrome with increased sensitivity to radiation.

The investigators wish to evaluate which cases and for which tumor types, 18F-FET PET/MRI will increase sensitivity and specificity of diagnosing CNS tumors.

Side effects The side effects are mainly the side effect from the MRI with venous puncture, the MRI contrast leading that can lead to shortlived nausea or headache, fasting for 6 hours and the radioactivity exposure of 4.2 mSv (1,4 times the early background radiation) for each scan procedure. The maximal number of scans in the project is 3, 6 or 10 depending on the diagnosis.

Data Analysis The correlation between 18F-FET uptake in tumor and tumor grading (obtained from operation/biopsy) will be investigated.

When relapse is suspected, sensitivity and specificity for recurrence/progression for MRI alone versus PET/MRI will be compared.

It will be analysed if the addition of PET influences the diagnosis/chosen treatment. A major impact of 6% will be regarded significant.

The prognostic value of 18F-FET uptake after treatment will be investigated.

02

Conditions studied

  • Positron-Emission Tomography
  • Brain Neoplasms, Childhood

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Keywords

  • FET
  • PET/MRI
  • child
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Suspicion of newly diagnosed CNS tumor, recurrence or radiation therapy planning
  • age \<18 years at first CT/MRI suggesting CNS tumor
  • written informed consent from parents (age \< 18 years) or the patient (age >18 years)

Exclusion criteria

Exclusion Criteria:

  • contraindications for MRI (e.g. metal implants)
  • pregnancy
  • known syndrome with increased sensitivity to radiation (e.g. Gorlin or Ataxia Telangiectasia
04

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    All included patients

    A 18F-FET PET scan is performed

    Diagnostic Test: 18F-FET PET

Interventions

  • Diagnostic test18F-FET PET

    Patient are investigated with an 18F-FET PET

05

What researchers measure

Primary outcomes

  1. Change of treatment

    The treatment plan is changed based on the PET findings

    Time frame: up to 3 months

Secondary outcomes

  1. Sensitivity and specificity

    The sensitivity and specificity of PET/MRI is compared to MRI alone. The gold standard is clinical follow-up.

    Time frame: up to 3 months

  2. Recurrence free survival time

    Comparison of PET better than MRI can predict the time before progression or recurrence

    Time frame: at least one year

06

Study locations

1 of 1 sites recruiting
  • Copenhagen University Hospital Rigshospitalet
    Copenhagen, Copenhagen O DK-2100, Denmark
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03402425
Lead sponsor
Rigshospitalet, Denmark
Collaborators
Børnecancerfonden
Responsible party
Lisbeth Marner (MD, PhD, DMSc, Staff Specialist, Rigshospitalet, Denmark) — Principal investigator
First posted
Jan 18, 2018
Start date
Feb 24, 2015
Primary completion
Dec 31, 2020 (estimated)
Completion
Dec 31, 2020 (estimated)
Last update
Mar 28, 2019

Study contacts

Lisbeth Marner, MD PhD DMSc
Contact
lisbeth.marner.01@regionh.dk
0045 35450968
Ian Law, MD PhD DMSc
Contact
ian.law@regionh.dk
0045 35458513
Lisbeth Marner, MD PhD DMSc
principal investigator · Rigshospitalet, Denmark

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Mar 2019. You cannot join it, but the record below documents what was studied.

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