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Trial Title:
Correlation Between SPECT/CT and IDH Mutation in Brain Glioma
NCT ID:
NCT05595863
Condition:
Brain Glioma
Conditions: Official terms:
Glioma
Study type:
Observational
Overall status:
Unknown status
Study design:
Time perspective:
Prospective
Summary:
Major advances in cancer genetics over the past decade have revealed that the genes
encoding IDHs are frequently mutated in a variety of human malignancies, including
gliomas.Pentavalent 99mTc dimercaptosuccinic acid (99mTc (V) DMSA), is a nonspecific
tumor targeting SPECT radiotracer, that has been used for imaging of various tumors
including lung and breast carcinoma. However, to date, scarce reports discussed the
utility of DMSA-V in patients with glioma.SPECT has the advantages of being widely
available and not expensive. Multiple SPECT tracers have been explored. Of them
Thallium-201 and 99 mTc-MIBI are, possibly, the most extensively discussed.
Detailed description:
Every year, nearly100,000 people worldwide are diagnosed as having brain gliomas.
Although it comprises <1% of all newly diagnosed cancers, brain glioma is associated with
substantial mortality and morbidity. Gliomas are intrinsic brain tumors that originate
from neuroglial progenitor cells. Conventional therapies, including surgery,
chemotherapy, and radiotherapy, have achieved limited improvements in the prognosis of
glioma patients.
Radiation therapy to the brain may lead to postradiation injury which typically occurs
within the first 3 to 12 months after radiotherapy but it was reported up to several
years and even decades later. The clinical picture of radiation necrosis (RN) is variable
and may include seizures, headache, personality changes, and neurologic deficits. These
symptoms mimic tumor recurrence and differentiation between the two entities clinically
or even by conventional radiological modalities is difficult but is necessary because the
two conditions have different treatment modalities and prognosis.
SPECT has the advantages of being widely available and not expensive. Multiple SPECT
tracers have been explored. Of them Thallium-201 and 99 mTc-MIBI are, possibly, the most
extensively discussed. The main disadvantage of 201Tl is the lower spatial resolution,
relatively large radiation dose, and the reported high false positive results. Normal
uptake of MIBI in the choroid plexus may be confounding for assessing tumors around the
ventricles.
Pentavalent 99mTc dimercaptosuccinic acid (99mTc (V) DMSA), is a nonspecific tumor
targeting SPECT radiotracer, that has been used for imaging of various tumors including
lung and breast carcinoma. However, to date, scarce reports discussed the utility of
DMSA-V in patients with glioma.
Isocitrate dehydrogenase (IDH) enzymes, of which there are three isoforms, are essential
enzymes that participate in several major metabolic processes, such as the Krebs cycle,
glutamine metabolism, lipogenesis and redox regulation.
Major advances in cancer genetics over the past decade have revealed that the genes
encoding IDHs are frequently mutated in a variety of human malignancies, including
gliomas, acute myeloid leukaemia, cholangiocarcinoma, chondrosarcoma and thyroid
carcinoma.
Criteria for eligibility:
Study pop:
Glioma patients visiting the nuclear medicine unit in Assiut university hospital.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- Patients with a pathologically proven glioma.
- patients conscious to provide informed consent.
Exclusion Criteria:
- Pregnant women.
- severely ill patients and those with disturbed conscious level,
- patients who were judged that they cannot lie down comfortably without movement for
at least 20 min..
Gender:
All
Minimum age:
N/A
Maximum age:
N/A
Healthy volunteers:
No
Start date:
November 2022
Completion date:
December 2023
Lead sponsor:
Agency:
Assiut University
Agency class:
Other
Source:
Assiut University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05595863
https://pubmed.ncbi.nlm.nih.gov/31227792/
https://pubmed.ncbi.nlm.nih.gov/21912937/
https://pubmed.ncbi.nlm.nih.gov/20143189/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250901/
https://pubmed.ncbi.nlm.nih.gov/15586883/