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glioblastoma classical subtype

ICD-10 Codes

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Description

Characteristics of Glioblastoma Classical Subtype

The glioblastoma classical subtype, also known as classical glioblastoma, is a molecular subtype of glioblastoma characterized by specific genetic and epigenetic features. According to [3], this subtype lacks p53 mutations, chromosome 7 amplifications or deletions, and has high levels of EGFR amplification.

Key Features

  • Lack of p53 mutations: Unlike other subtypes, the classical subtype does not harbor p53 mutations, which are common in glioblastoma [9].
  • High-level EGFR amplification: The classical subtype is characterized by high levels of EGFR amplification, with over one-third of cases showing EGFR mutation [9].
  • Chromosome 7 amplifications or deletions: Unlike other subtypes, the classical subtype does not have chromosome 7 amplifications or deletions.

Implications

The glioblastoma classical subtype is distinct from other subtypes and has implications for treatment and prognosis. Further research is needed to fully understand the characteristics of this subtype and its potential therapeutic targets.

References:

[3] - A molecular subtype of glioblastoma characterized by lack of p53 mutations, chromosome 7 amplifications or deletions, and high levels of EGFR amplification. [9] - In the classical subtype, 97% of gliomas harbored high-level EGFR amplification, with EGFR mutation seen in over one-third of cases.

Additional Characteristics

  • Lack of p53 mutations
  • High-level EGFR amplification
  • Chromosome 7 amplifications or deletions

Signs and Symptoms

Based on my analysis, I was unable to find any relevant information in the search results that directly answers your query about the signs and symptoms of glioblastoma classical subtype.

However, I can suggest some general information about glioblastoma. Glioblastoma is a type of brain cancer that is known for its aggressive growth and poor prognosis. It is typically characterized by a combination of symptoms such as:

  • Headaches: These are often the first symptom of glioblastoma, and may be severe and persistent.
  • Seizures: Seizures can occur in up to 30% of patients with glioblastoma, especially if the tumor is located in an area that affects seizure activity.
  • Weakness or numbness: Patients may experience weakness or numbness on one side of their body, which can be due to the tumor's location and growth pattern.
  • Vision changes: Glioblastomas can cause vision problems, such as blurred vision, double vision, or loss of peripheral vision.
  • Personality changes: Some patients with glioblastoma may experience personality changes, such as depression, anxiety, or irritability.

It is essential to note that these symptoms are not specific to glioblastoma and can be caused by other conditions. A definitive diagnosis of glioblastoma requires a combination of imaging studies (such as MRI or CT scans), biopsy, and histopathological examination.

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Additional Symptoms

  • Seizures
  • Vision changes
  • Headaches
  • Personality changes
  • weakness

Diagnostic Tests

Based on the search results, it appears that there are several diagnostic tests and characteristics associated with the classical subtype of glioblastoma (GBM).

  • EGFR amplification: EGFR amplification is a common feature in patients with the classical subtype of GBM [8]. This genetic alteration can be detected through various molecular tests.
  • Genetic profiling: Integrated genomic analysis has identified clinically relevant subtypes of glioblastoma, including the classical subtype, characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1 [5].
  • Imaging studies: Diagnostic imaging techniques such as MRI and CT scans can help identify the location and extent of the tumor. However, these tests may not be able to distinguish between different subtypes of GBM.
  • Gene expression analysis: Gene expression-based molecular classification has been used to identify the classical subtype of GBM [3]. This approach involves analyzing the expression levels of specific genes to determine the subtype.

It's worth noting that a robust gene expression-based molecular classification of GBM into Proneural, Neural, Classical, and Mesenchymal subtypes has been described in the literature [3].

References:

[3] by RGW Verhaak · 2010 · Cited by 8155 [8] by W Szopa · Cited by 374

Additional Diagnostic Tests

  • Imaging studies
  • EGFR amplification
  • Genetic profiling
  • Gene expression analysis

Treatment

Treatment Options for Glioblastoma Classical Subtype

Glioblastoma (GBM) classical subtype is one of the four subtypes of GBM, and it has a distinct molecular profile. The treatment options for this subtype are similar to those for other types of glioblastoma, but with some nuances.

Current Standard Therapy

The current standard therapy for GBM classical subtype includes maximal safe surgical resection followed by concurrent radiation therapy and chemotherapy (temozolomide) [12]. This approach has been shown to improve survival rates in patients with this subtype.

Temozolomide Response

Studies have shown that the response to temozolomide in Classical and Mesenchymal subtypes is higher than that of neurotypes, and the Proneural subtype is lower than that of classical subtype [5]. This suggests that temozolomide may be a more effective treatment option for patients with GBM classical subtype.

Other Treatment Options

Other repositioned drugs for GBM include gemcitabine and cytarabine which are currently approved for other solid tumors. Cytarabine (Ara-C) is another drug that has been shown to have some efficacy in treating glioblastoma [7].

Challenges and Future Directions

Despite the advances in treatment options, GBM classical subtype remains a challenging disease to treat. Further research is needed to develop more effective treatments for this subtype.

References:

  • [12] A study on the current standard therapy for GBM classical subtype.
  • [5] A study on the response of temozolomide in different subtypes of glioblastoma.
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Differential Diagnosis

Understanding Differential Diagnosis in Glioblastoma

The differential diagnosis of glioblastoma (GBM) refers to the process of ruling out other possible conditions that may present with similar symptoms or characteristics as GBM. In the context of the classical subtype, the differential diagnosis is crucial for accurate diagnosis and treatment planning.

Key Conditions to Consider

According to recent studies [5][15], the following conditions should be considered in the differential diagnosis of glioblastoma classical subtype:

  • Astrocytoma: A type of brain tumor that can present with similar symptoms as GBM.
  • Oligodendroglioma: Another type of brain tumor that may be confused with GBM due to overlapping characteristics.
  • Cerebral Metastasis: The presence of cancer cells in the brain, which can mimic the symptoms of GBM.
  • Primary CNS lymphoma: A rare type of brain cancer that should be ruled out in cases where GBM is suspected.

Importance of Accurate Diagnosis

Accurate diagnosis of glioblastoma classical subtype is critical for determining the best course of treatment and improving patient outcomes. The differential diagnosis process helps clinicians to rule out other conditions, thereby ensuring that patients receive the most appropriate care.

References:

[5] by R Chen · 2017 · Cited by 715 — The gene expression subtypes were called classic, mesenchymal, proneural, and neural. In the classical subtype, 97% of gliomas harbored high ...

[15] by G Marziali · 2016 · Cited by 103 — The two clusters are also differentiated by NMR spectroscopy profiles suggesting a potential prognostic stratification based on metabolic ...

Additional Differential Diagnoses

Additional Information

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