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Uncommon low-grade brain tumors
Thankamma Ajithkumar1, Naduni Imbulgoda2, Elliott Rees3
1Department of Oncology, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, UK.
Abstract:
The 2016 World Health Organization (WHO) classification of primary central nervous system (CNS) tumors includes numerous uncommon (representing ≤1% of tumors) low-grade (grades I-II) brain neoplasms with varying clinical behaviors and outcomes. Generally, gross tumor or maximal safe resection is the primary treatment. Adjuvant treatments, though their exact role is unknown, may be considered individually based on pathological subtypes and a proper assessment of risks and benefits. Targetable mutations such as BRAF (proto-oncogene B-Raf), TRAIL (tumor necrosis factor apoptosis inducing ligand), and PDGFR (platelet derived growth factor receptor) have promising roles in future management.
Insights
This study reviews uncommon low-grade brain tumors classified by the WHO. Future management may involve targeted therapies based on specific genetic mutations like BRAF.
Area of Science:
- Neuro-oncology
- Pathology
- Genetics
Background:
- The 2016 World Health Organization (WHO) classification details rare low-grade (grades I-II) primary central nervous system (CNS) tumors.
- These neoplasms exhibit diverse clinical behaviors and prognoses.
Purpose of the Study:
- To summarize the current understanding of uncommon low-grade CNS tumors.
- To highlight the primary treatment modalities and the potential role of adjuvant therapies.
- To discuss emerging targeted mutations for future therapeutic strategies.
Main Methods:
- Review of the 2016 WHO classification of CNS tumors.
- Analysis of treatment principles for low-grade brain neoplasms.
- Identification of targetable mutations relevant to CNS tumor management.
Main Results:
- Gross total or maximal safe tumor resection is the standard primary treatment.
- The role of adjuvant treatments requires individualized assessment based on pathological subtypes and risk-benefit analysis.
- Mutations in BRAF (proto-oncogene B-Raf), TRAIL (tumor necrosis factor apoptosis inducing ligand), and PDGFR (platelet derived growth factor receptor) show promise for targeted therapies.
Conclusions:
- Management of uncommon low-grade CNS tumors relies on surgical resection and individualized adjuvant strategies.
- Targeted therapies focusing on mutations like BRAF, TRAIL, and PDGFR represent a promising frontier in neuro-oncology.
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