Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34322
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dc.contributor.authorKweh, Barry Ting Sheen-
dc.contributor.authorAsaid, Mina-
dc.contributor.authorKhoo, Boyuan-
dc.contributor.authorDonaldson, Christopher-
dc.contributor.authorLokan, Julie-
dc.contributor.authorGan, Hui K-
dc.contributor.authorGonzalvo, Augusto Carlos-
dc.date2023-
dc.date.accessioned2023-12-01T02:13:36Z-
dc.date.available2023-12-01T02:13:36Z-
dc.date.issued2023-11-24-
dc.identifier.citationJournal of Neurosurgery 2023-11-24en_US
dc.identifier.issn1933-0693-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34322-
dc.description.abstractThe rarity of intracranial extraventricular neurocytomas (EVNs) has precluded accurate definition of its surgical characteristics to date. The authors present the first survival analysis of this unique entity that aims to clarify tumor characteristics, surgical outcomes, and efficacy of postoperative adjuvant therapy. A systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Searches of the MEDLINE, Embase, Scopus, Google Scholar, and Cochrane Database of Systematic Reviews databases were performed from inception to date. Primary outcomes were progression-free survival (PFS) and overall survival (OS). Prognostic variables were age, sex, tumor consistency, extent of resection, and receipt of postoperative adjuvant therapy. Survival data were analyzed using Kaplan-Meier survival curves and the log-rank test to compare dichotomized cohorts. Multivariate Cox regression models were constructed, interrogated with Schoenfeld residuals, and subsequently utilized to identify independent prognostic factors. Risk of bias was assessed with the Mayo Clinic instrument. Five hundred fourteen articles were initially retrieved, which was distilled to 10 included articles consisting of 101 cases of intracranial EVNs. The 5-year OS rate was 90.4% (95% CI 81.8%-99.8%) and the PFS rate was 48.6% (95% CI 34.46%-68.8%). The median PFS was 60 months. Patients younger than 50 years of age experienced superior OS (p = 0.03) and PFS (p < 0.01). Gross-total resection (GTR) was superior to subtotal resection (STR) in reducing mortality (p < 0.01). Adjuvant therapy following either STR or GTR did not significantly improve survival. Intracranial EVNs are rare tumors that portend a poorer prognosis than central neurocytomas, despite both being WHO grade 2 tumors. Complete surgical extirpation is the cornerstone of management. There is no clearly established role for adjuvant postoperative therapy, but each case should be managed on an individual basis.en_US
dc.language.isoeng-
dc.subjectchemotherapyen_US
dc.subjectextraventricular neurocytomaen_US
dc.subjectneuro-oncologyen_US
dc.subjectoverall survivalen_US
dc.subjectresectionen_US
dc.subjecttumoren_US
dc.titleSurvival outcomes of intracranial extraventricular neurocytomas: a systematic review and individual patient data meta-analysis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Neurosurgeryen_US
dc.identifier.affiliationNational Trauma Research Institute, Melbourne.en_US
dc.identifier.affiliationDepartment of Neurosurgery, Alfred Hospital, Melbourne.en_US
dc.identifier.affiliationNeurosurgeryen_US
dc.identifier.affiliationDepartments of4Anatomical Pathologyen_US
dc.identifier.affiliationDepartment of Surgery, University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.doi10.3171/2023.8.JNS231640en_US
dc.type.contentTexten_US
dc.identifier.pubmedid38000064-
dc.description.startpage1-
dc.description.endpage11-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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