Prognostic Factors of Low-Grade Gliomas in Adults.

Adult low-grade gliomas are a rare and aggressive pathology of the central nervous system. Some of their characteristics contribute to the patient's life expectancy and to their management. This study aimed to characterize and identify the main prognostic factors of low-grade gliomas. The six-year r...

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Published in:Current Oncology Vol. 29; no. 10; pp. 7327 - 7343
Main Authors: Deacu, Mariana, Popescu, Steliana, Docu Axelerad, Any, Topliceanu, Theodor Sebastian, Aschie, Mariana, Bosoteanu, Madalina, Cozaru, Georgeta Camelia, Cretu, Ana Maria, Voda, Raluca Ioana, Orasanu, Cristian Ionut
Format: Journal Article
Published: MDPI Oct2022
Online Access:View this record in EBSCOhost
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      dt: Oct2022
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      pub: MDPI
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        10.3390/curroncol29100576
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        atl: Prognostic Factors of Low-Grade Gliomas in Adults.
      aug:
        au:
          Deacu, Mariana
          Popescu, Steliana
          Docu Axelerad, Any
          Topliceanu, Theodor Sebastian
          Aschie, Mariana
          Bosoteanu, Madalina
          Cozaru, Georgeta Camelia
          Cretu, Ana Maria
          Voda, Raluca Ioana
          Orasanu, Cristian Ionut
        affil: Clinical Service of Pathology, Departments of Pathology, Sfantul Apostol Andrei Emergency County Hospital, 900591 Constanta, Romania
      sug:
      ab: Adult low-grade gliomas are a rare and aggressive pathology of the central nervous system. Some of their characteristics contribute to the patient's life expectancy and to their management. This study aimed to characterize and identify the main prognostic factors of low-grade gliomas. The six-year retrospective study statistically analyzed the demographic, imaging, and morphogenetic characteristics of the patient group through appropriate parameters. Immunohistochemical tests were performed: IDH1, Ki-67, p53, and Nestin, as well as FISH tests on the CDKN2A gene and 1p/19q codeletion. The pathology was prevalent in females, with patients having an average age of 56.31 years. The average tumor volume was 41.61 cm3, producing a midline shift with an average of 7.5 mm. Its displacement had a negative impact on survival. The presence of a residual tumor resulted in decreased survival and is an independent risk factor for mortality. Positivity for p53 identified a low survival rate. CDKN2A mutations were an independent risk factor for mortality. We identified that a negative prognosis is influenced by the association of epilepsy with headache, tumor volume, and immunoreactivity to IDH1 and p53. Independent factors associated with mortality were midline shift, presence of tumor residue, and CDKN2A gene deletions and amplifications.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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