Gliomas: Difference between revisions
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==Low Grade Glioma== | ==Low Grade Glioma== | ||
<div class="card"> | <div class="card"><div class="card-header"> | ||
<h3 class="card-title">Outlines from Neurosurgery Self-assessment - Q&A</h3> | <h3 class="card-title">Outlines from Neurosurgery Self-assessment - Q&A</h3> | ||
</div> | </div> | ||
*1° goal in initial Tx of LGG is max. safe resection → assoc. w/ prolonged survival, sz pPx, ↓ risk of transformation; | *1° goal in initial Tx of LGG is max. safe resection → assoc. w/ prolonged survival, sz pPx, ↓ risk of transformation; | ||
*Qx for suspected LGGs challenges: | *Qx for suspected LGGs challenges: | ||
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**Histopathological undergrading is common w/ Bx, as LGG often exhibits focal areas of malignant transformation (anaplastic foci). To avoid this and reduce subsequent treatment failure, the surgical goal is to perform precise tissue sampling from a potential anaplastic focus. | **Histopathological undergrading is common w/ Bx, as LGG often exhibits focal areas of malignant transformation (anaplastic foci). To avoid this and reduce subsequent treatment failure, the surgical goal is to perform precise tissue sampling from a potential anaplastic focus. | ||
**"Eloquent" localization → awake Qx ± functional mapping | **"Eloquent" localization → awake Qx ± functional mapping | ||
</div> | </div> | ||
==High Grade Glioma== | ==High Grade Glioma== | ||
Revision as of 02:26, 19 August 2023
Low Grade Glioma
Outlines from Neurosurgery Self-assessment - Q&A
- 1° goal in initial Tx of LGG is max. safe resection → assoc. w/ prolonged survival, sz pPx, ↓ risk of transformation;
- Qx for suspected LGGs challenges:
- GTR is difficult d/t the diffusely infiltrative growth pattern of LGG → difficult to id the exact tumor borders; ∴ image guidance w/ FLAIR is crucial.
- Histopathological undergrading is common w/ Bx, as LGG often exhibits focal areas of malignant transformation (anaplastic foci). To avoid this and reduce subsequent treatment failure, the surgical goal is to perform precise tissue sampling from a potential anaplastic focus.
- "Eloquent" localization → awake Qx ± functional mapping
High Grade Glioma
Molecular markers in Gliomas
O(6)-Methylguanine-DNA Methyltransferase (MGMT)
- The O(6)-Methylguanine-DNA Methyltransferase (MGMT) is a DNA repair enzyme that counteracts the chemotherapeutic effects of alkylating agents.
- Cancer-related methylation of the MGMT promoter region results in less DNA repair activity, including that induced by temozolomide (TMZ).
- MGMT promoter methylation in GBM is a prognostic and predictive biomarker indicating response to chemoradiation.
- Patients with MGMT promoter methylated tumors benefit most from treatment with TMZ.
- Absence of MGMT promoter methylation → ↓ benefit from chemoradiation.
- MGMT promoter methylation is a useful predictive biomarker for stratifying elderly GBM patients for RT versus alkylating agent chemotherapy.
Telomerase Reverse Transcriptase (TERT)
- Telomeres, at the ends of chromosomes, shorten w/ each cell division - limit to cell replication.
- Telomerase, an enzyme that helps to maintain the length of telomeres;
- Gliomas can bypass this limit via overexpression of TERT due to mutations in the promoter.
- overactive TERT → maintaining telomere length → facilitating tumor expression
Isocitrate dehydrogenase (IDH) 1/2
- IDH 1 & 2 glu metabolism enzymes
- Mutations in IDH1/2 → abnml form of IDH enzyme → ↑ 2-hydroxyglutarate (2-HG)
- 2-HG is a toxic metabolite → promote tumor growth.
- IDH mutations assoc. w/ better prognosis (LGG)
- IDH wild type (no mutations of the IDH) - worse prognosis because assoc. w/ HGG