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Overview

Astrocytoma is a type of brain tumor that originates from astrocytes, the star-shaped glial cells in the brain and spinal cord that support and nourish neurons. Astrocytomas are part of a broader category known as gliomas and are classified based on their grade (I to IV), which reflects how fast the tumor grows and how likely it is to spread.

  • Grade I (Pilocytic Astrocytoma): Typically benign and slow-growing, often seen in children.
  • Grade II (Diffuse Astrocytoma): Infiltrative, slow-growing but may progress.
  • Grade III (Anaplastic Astrocytoma): Malignant, faster-growing.
  • Grade IV (Glioblastoma): Most aggressive form.

Symptoms

Symptoms vary depending on the tumor’s size and location in the brain but may include:

  • Headaches (often worse in the morning)
  • Seizures
  • Nausea and vomiting
  • Personality or behavior changes
  • Weakness or numbness in parts of the body
  • Difficulty with speech, vision, or coordination

Causes & Risk Factors

The exact causes of astrocytoma are not fully understood, but factors may include:

  • Genetic mutations (e.g., TP53, IDH1/IDH2)
  • Family history of gliomas
  • Radiation exposure (especially to the head during childhood)
  • Age: Low-grade tumors are more common in younger individuals, while high-grade forms are more frequent in adults

Diagnosis

Astrocytoma is diagnosed using:

  • MRI scan with contrast: To visualize the tumor’s location and characteristics
  • CT scan: Sometimes used for initial assessment
  • Biopsy: To determine the grade and molecular profile
  • Molecular testing: For IDH mutations, 1p/19q co-deletion, MGMT promoter methylation, and ATRX loss

Treatment Options

Treatment depends on the tumor grade, size, location, and genetic characteristics:

  • Surgery: Primary option for tumor removal
  • Radiation therapy: Often used for intermediate to high-grade tumors
  • Chemotherapy: Temozolomide is commonly used for Grade III and IV astrocytomas
  • Targeted therapy and clinical trials: For selected molecular subtypes
  • Observation: Sometimes recommended for asymptomatic low-grade tumors

Prognosis

Prognosis varies significantly by tumor grade:
• Grade I (Pilocytic): Excellent prognosis; high long-term survival
• Grade II (Diffuse): May remain stable for years, but often progresses
• Grade III (Anaplastic): Median survival 2–5 years
• Grade IV (Glioblastoma): Median survival ~12–15 months

Prognosis improves with younger age, complete surgical resection, and favorable molecular markers (e.g., IDH mutation, MGMT methylation).

Living with this Cancer Type

Prognosis varies significantly by tumor grade:

  • Grade I (Pilocytic): Excellent prognosis; high long-term survival
  • Grade II (Diffuse): May remain stable for years, but often progresses
  • Grade III (Anaplastic): Median survival 2–5 years
  • Grade IV (Glioblastoma): Median survival ~12–15 months

Prognosis improves with younger age, complete surgical resection, and favorable molecular markers (e.g., IDH mutation, MGMT methylation).

Prevention & Screening

  • No established screening protocol
  • Minimize unnecessary radiation exposure, especially in children
  • Genetic counseling for families with hereditary glioma syndromes (e.g., Li-Fraumeni)

FAQs

  • Q: Is astrocytoma cancerous?
  • A: Low-grade astrocytomas are considered benign or slow-growing. High-grade astrocytomas are malignant and aggressive.
  • Q: Can astrocytomas come back after treatment?
  • A: Yes, recurrence is common, especially in higher grades.
  • Q: Can children get astrocytoma?
  • A: Yes, particularly Grade I (pilocytic) astrocytomas are common in pediatric patients.
  • Q: What’s the difference between astrocytoma and glioblastoma?
  • A: Glioblastoma is a Grade IV astrocytoma — the most aggressive form.

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