New scan could reveal brain tumor aggression without surgery
NCT ID NCT00850278
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a special PET scan tracer called FLT in 50 adults with brain tumors (gliomas or metastases). The goal was to see if FLT-PET can measure how fast tumor cells are growing, which could help doctors diagnose and predict tumor behavior better than current scans like MRI or MET-PET. Participants received FLT-PET, MET-PET, and MRI before surgery, and results were compared with lab tests and survival data.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- FLT (a radioactive tracer for PET imaging)
- What this could lead to
- If successful, FLT-PET could become a better way to see how aggressive a brain tumor is without surgery, helping doctors plan treatment more accurately.
- What could go wrong
- This is a small, early imaging study (50 people) that only looks at whether the scan works, not whether it improves outcomes. The tracer may not be better than existing methods.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
50 people
The number who actually took part.
- Start date
-
Oct 2008
- Finished
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Jul 2011
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * adults aged between 18 and 70 years * must have operable grade II, III or IV glioma, recurrent high grade glioma or brain metastases * KPS \>= 70% * must have the understanding and ability to sign an informed consent document * must have adequate liver and kidney function * be male or non-pregnant, non-lactating females * patients who are fertile must agree to use an effective method of contraception during participation in the study * the following laboratory results : absolute neutrophil count \>= 1500 cells/µl, platelet count \>= 100000 cells/µl, SGOT \<= 2.5 x ULN, serum creatinine \<= 1.5 x ULN. Exclusion Criteria: * contraindication to surgery * concomitant radio-, chemo-, or immunotherapy * history of significant dementia * known diagnosis of Human Immunodeficiency Virus (HIV) infection * patient with hepatitis B or C
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Caen University Hospital
Caen, 14033, France
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