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Carbonic anhydrase IX is a prognostic biomarker in glioblastoma multiforme

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Date

2018

Author

Çetin, Bülent
Gönül, İpek Işık
Gumusay, Özge
Bilgetekin, İrem
Algın, Efnan
Özet, Ahmet
Üner, Aytuğ

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Cetin, B., Gonul, I. I., Gumusay, O., Bilgetekin, I., Algin, E., Ozet, A., & Uner, A. (2018). Carbonic anhydrase IX is a prognostic biomarker in glioblastoma multiforme. Neuropathology : official journal of the Japanese Society of Neuropathology, 38(5), 457–462. https://doi.org/10.1111/neup.12485

Abstract

The identification of prognostic factors in patients with glioblastoma multiforme (GBM) represents an area of increasing interest. Carbonic anhydrase IX (CA-IX), a hypoxia marker, correlates with tumor progression in a variety of human cancers. However, the role of CA-IX in GBM remains largely unknown. in the present study, we evaluated the prognostic role of CA-IX in GBM patients. in total, 66 consecutive patients with GBM who received concomitant chemoradiotherapy and adjuvant chemotherapy with temozolomide were retrospectively reviewed, and all patients received temozolomide chemotherapy for at least 3 months. Kaplan-Meier curves and log-rank tests were used for analysis of progression-free survival (PFS) and overall survival (OS), and a multivariate Cox proportional hazard model was employed to identify factors with an independent effect on survival. the median OS was longer in patients with low levels of CA-IX expression (18 months) compared to patients overexpressing CA-IX (9 months) (P = 0.004). There was not a statistically significant difference in median PFS (3.5 vs. 8 months, P = 0.054) between patients with high or low levels of CA-IX expression. in multivariate analysis, the variables that were identified as significant prognostic factors for OS were preoperative Karnofsky performance scale score (KPS) (hazard ratio (HR), 3.703; P = 0.001), CA-IX overexpression (HR, 1.967; P = 0.019), and incomplete adjuvant temozolomide treatment (HR, 2.241; P = 0.003) and gross-total resection (HR, 1.956; P = 0.034). Our findings indicated that CA-IX may be a potential prognostic biomarker in the treatment of GBM.

Source

Neuropathology

Volume

38

Issue

5

URI

https://doi.org/10.1111/neup.12485
https://hdl.handle.net/11436/1751

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  • PubMed İndeksli Yayınlar Koleksiyonu [2443]
  • Scopus İndeksli Yayınlar Koleksiyonu [6032]
  • TF, Dahili Tıp Bilimleri Bölümü Koleksiyonu [1574]
  • WoS İndeksli Yayınlar Koleksiyonu [5260]



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