Published online May 24, 2026. doi: 10.5306/wjco.v17.i5.118350
Revised: January 10, 2026
Accepted: March 9, 2026
Published online: May 24, 2026
Processing time: 141 Days and 20.1 Hours
Gliomas, the most prevalent primary malignant brain tumours, display rem
To evaluate the association of nestin expression, tumour grade, and survival in glioma patients from Pakistan.
This prospective cohort study included 128 histologically confirmed glioma cases (64 low-grade; 64 high-grade) diagnosed at Prime Teaching Hospital, a tertiary care teaching hospital in Khyber Pakhtunkhwa, Pakistan, between January 2023 and September 2024. Nestin expression was evaluated by immunohistochemistry using the Im
High-grade tumours exhibited higher nestin overexpression rates compared to low-grade gliomas (90.6% vs 70.3%, P = 0.004), and the median overall survival was 3 months for high-grade tumours and 26 months for low-grade tumours. In patients with high nestin expression, shorter survival (8 months) was seen, while those with low expression showed longer survival (22 months, P = 0.025). When analysed in combination, a trend towards the poorest prognosis in high-grade gliomas with high nestin (median 2 months) and the best in low-grade with low nestin (26 months, P = 0.001) was observed. No significant association was observed with patients’ gender, age, or tumour site.
Nestin overexpression is associated with higher glioma grade and poorer overall survival across astrocytic and oligodendroglial tumors and may serve as a supplementary prognostic biomarker, particularly in settings with limited access to molecular diagnostics.
Core Tip: Gliomas show marked biological heterogeneity, necessitating accessible prognostic biomarkers, especially in resource-limited settings. This prospective study demonstrates that nestin overexpression is significantly associated with higher tumour grade and inferior overall survival in both low- and high-grade gliomas. High-grade tumours showed markedly increased nestin expression and substantially shorter survival compared to low-grade counterparts. Patients with high nestin expression experienced poorer outcomes, while the combined analysis revealed the worst prognosis in high-grade gliomas with high nestin levels. These findings highlight nestin as a practical supplementary prognostic marker that may aid risk stratification where advanced molecular testing is unavailable.