Neuro-Oncology· 2026Q1
Piloritrik özellikli yüksek dereceli astrositom: Geniş bir kohort kullanılarak prognostik faktörlerin klinik ve genomik analizi
High-grade astrocytoma with piloid features: a clinical and genomic analysis of prognostic factors using a large cohort
- 0atıf
- Q1SCImago
- 2026yıl
Kısa özet
Daha ileri yaş (p=0.01), ATRX alterasyonu (p=0.04) ve MRG'de kistik özellikler (p=0.01), yüksek dereceli piloritrik özellikli astrositom (HGAP) için prognostik faktörlerdir.
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Ana noktalar
- Daha ileri yaş (p=0.01) ve ATRX alterasyonu (p=0.04), HGAP için olumsuz prognostik faktörlerdir.
- MRG'deki kistik özellikler olumlu bir prognostik faktördür (p=0.01).
- HGAP'da yüksek oranlarda ATRX alterasyonu (%62), CDKN2A/B homozigot kaybı (%78) ve MGMT promoter metilasyonu (%53) gözlemlenmiştir.
- Değerlendirilebilir örneklerin %74'ünde MAPK alterasyonları tespit edilmiştir.
- Histolojik yüksek derece özellikleri, CDKN2A/B homozigot delesyonu, MGMT metilasyonu ve rezeksiyonun kapsamı prognostik olarak anlamlı değildi.
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Özet (abstract)
Abstract Background High-grade astrocytoma with piloid features (HGAP) is a recently defined tumor type that is not well-understood. Prognostic factors of clinical outcomes are not well-established. Methods Methylation profiling was performed on tumor samples, many at the National Cancer Institute (NCI) Laboratory of Pathology, and others from publicly available sources. Methylation classifier scores of ≥ 0.90 to the HGAP class on the NCI-Bethesda classifier version 3 were included. Clinical features were collected from the medical record. Survival analyses were performed using the Kaplan-Meier and Cox-proportional hazards methods. Results The cohort comprised 421 patients. There were high rates of ATRX alteration (62%), CDKN2A/B homozygous loss (78%) and MGMT promoter methylation (53%). MAPK alterations were identified in 74% of evaluable samples. The median age was 46 years, and posterior fossa location was predominant (52%). The median overall survival (OS) was 88 months. Older age (p = 0.01) and the presence of an ATRX alteration (p = 0.04) were found to be negative prognostic factors. The presence of cystic features on magnetic resonance imaging (MRI) was found to be favorably prognostic (p = 0.01). Factors that were not significantly associated with prognosis included histologic high-grade features, CDKN2A/B homozygous deletion, MGMT promoter methylation, extent of resection, and presence of NF1 syndrome. Conclusions This large cohort establishes relative frequencies of several important markers. Additionally, older age, the presence of an ATRX alteration, and cystic features on MRI were found to be prognostic. Our work may aid in optimizing treatment regimens for patients with this tumor type.
Yazarların özeti; kaynağından alınmıştır. Neuro-Oncology, 2026 · DOI ↗
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Alan: Genetik (Tıp)
GeneticsMedicine