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Trial Title:
Application of MET-PET in Fusion With MRI in the Treatment of Glioblastoma Multiforme
NCT ID:
NCT06466031
Condition:
Glioblastoma Multiforme
Conditions: Official terms:
Glioblastoma
Conditions: Keywords:
Glioblastoma Multiforme
Methionine
Positron-Emission Tomography
Brain neoplasms
Progression-free survival
Dose Fractionation, Radiation
Post-surgical radiotherapy
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Treatment
Masking:
Double (Investigator, Outcomes Assessor)
Intervention:
Intervention type:
Other
Intervention name:
MRI & PET fusion
Description:
MRI+T1C in fusion with MET-PET will be used for tumor resection and/or radiotherapy
planning. Resection will be terminated after removal of PET-assigned tumor margin or in
case any neuromonitoring-based indications regarding neurological damage occur.
Arm group label:
Radiotherapy according to the MRI & PET fusion
Arm group label:
Resection and radiotherapy according to the MRI & PET fusion
Intervention type:
Other
Intervention name:
MRI+T1C
Description:
MRI+T1C will be used for tumor resection and radiotherapy planning. Resection will be
terminated after removal of contrast-enhancing part regardless of 5-ALA fluorescence or
in case any neuromonitoring-based indications regarding neurological damage occur.
Arm group label:
Radiotherapy according to the MRI & PET fusion
Arm group label:
Resection and radiotherapy according to the MRI
Summary:
Glioblastoma multiforme (GBM IV WHO) is the most common, primary neoplasm of brain in the
adults. Simultanously it is the most agressive one of all primary brain tumors. Despite
the treatment the outcome in that group of patients is poor. In case of the optimal
therapy the estimated median of survival ranges between 12 and 16 months. The present
standard of treatment embraces the gross total resection with the preserved neurological
functions and the posoperative management according to the Stupp's protocol (fractionated
radiotherapy of 60 Gy dose and the chemotherapy with Temozolamide).
Annually the incidence rate of GBM is 5/100.000 of population. According to the National
Tumor Registry 2494 people went down to the malignant neoplasmatic disease of brain
classified as C71 (ICD-10) in 2020. The evaluation indicates that it is 600 new patients
with the diagnosis of GBM. The disease becomes the 9th cause of death among males and the
13th one among females. The peak of incidence appears in the 5th decade of life and
concerns the most productive population. Routinely the management embraces the planning
of the resection surgery based on the preoperative magnetic resonance investigation (MRI)
with contrast. The common image of the tumor allows to put the preliminary diagnosis with
the high probability rate. The GBM occurs as the enhanced tumor with the central necrosis
and the circumferential brain edema visible in T2 and Flair sequences of MRI. Commonly
the border of tumor becomes the line of contrast enhancement. The enhances area is the
aim of surgical treatment. The lack of the preoperative enhanced area in the
postoperative MRI is assumed as the gross total resection (GTR). It has been proved that
the range of the resection translates into the overall survival (OS) and the progression
free survival (PFS). Despite the resection classified as GTR the relapse in the operated
area often occurs. It can be explained by the presence of the glioma stem cells in the
surrounding neuronal tissue. They are responsible for the early relapse of GBM. Notably,
it is evident that the MRI with contrast becomes the method which does not reveal the
proper range of resection with the relevant sensitivity so as to extend PFS and OS. The
positron emission tomography (PET) is one of the diagnostic methods having been
clinically evaluated. PET assesses the metabolic demand of the neoplasm for the
biochemical substrates. That methodology is commonly used in case of severity of the
solid tumors. The fluorodeoxyglucose (18-FDG) is the most frequently used. However the
high metabolism of glucose within the brain, particularly in the grey matter, 18-FDG has
the limitation in the process of planning of the tumor resection. The higher specificity
and sensitivity are elicited among the markers including aminoacids, praticularly 11-C
methionine (11C-MET). Within the gliomas the higher uptake is observed than in the
healthy brain. The range of the contrast enhancement in the MRI covers only 58% of the
higher 11C-MET metabolism. Comparing these results with a tumor resection beyond the
enhancement area, indicates the necessity of the precise assessment of the proposed
method in the routine planning of the glioma resection.
Current body of literature lacks in high quality research concerning that issue. The
articles regarding the glioma resection beyond the GTR may be found instead. The surgery
is limited to the resection of brain area with the incorrect signal in the FLAIR
sequence, suspected of the presence of glioma stem cells. The described technique allows
to extend PFS by for about 2 months. In that case the resection is based mainly on the
FLAIR sequence which does not determine the presence of the neoplasm therein. The fusion
of the MRI and the MET-PET images would allow to plan the resection so as to cover the
area of incorrectly increased marker uptake.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Single macroscopic tumor focus with the appearance of glioblastoma multiforme on MRI
with contrast - contrast-enhancing lesion, completely or with central necrosis, with
surrounding edema.
- No history of cancer in other organs. No suspicious lesions on X-ray of the chest
and abdomen (CT with contrast).
- No clinical suspicion of brain abscess - no meningeal symptoms, signs of
neuroinfection, fever, elevated inflammatory parameters.
- Primary tumor, without neurosurgical, radiotherapy or oncology intervention. Prior
tumor biopsy is allowed.
- Tumor eligible for surgical treatment - craniotomy and tumor resection.
- Age ≥ 18 years but < 70 years old.
- Quality of life assessment: KPS ≥ 70.
- Informed patient consent to the study and proposed treatment.
- No allergy to contrast agents used in PET and MRI.
- No medical contraindications to neurosurgery - craniotomy and resection.
Exclusion Criteria:
- Multifocal brain tumor.
- Recurrence of glioblastoma multiforme.
- Clinical or radiological suspicion of brain metastasis or brain abscess.
- Postoperative histopathological diagnosis other than WHO grade IV glioblastoma.
- Medical contraindications to any surgery under general anesthesia.
- Pregnancy, breastfeeding.
- Known allergy to gadolinium contrast or radiopharmaceutical tracing agent.
Gender:
All
Minimum age:
18 Years
Maximum age:
70 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
Copernicus Memorial Hospital in Łódź, Poland
Address:
City:
Łódź
Zip:
93-513
Country:
Poland
Contact:
Last name:
Kamil Krystkiewicz, PhD
Phone:
+48426895341
Email:
kamil.krystkiewicz@gmail.com
Start date:
September 1, 2024
Completion date:
July 31, 2032
Lead sponsor:
Agency:
Copernicus Memorial Hospital
Agency class:
Other
Collaborator:
Agency:
Medical Research Agency, Poland
Agency class:
Other
Source:
Copernicus Memorial Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06466031