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The impact of these genetic alterations on overall survival (<jats:styled-content style=\"fixed-case\">OS<\/jats:styled-content>) and progression free survival (<jats:styled-content style=\"fixed-case\">PFS<\/jats:styled-content>) was evaluated.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>A cohort of 80 patients surgically treated at Hospital Cl\u00ednico San Carlos, Madrid, between March 2004 and November 2012, was analyzed. Tumors were distributed in 73 primary brain tumors (gliomas, meningiomas, hemangiopericytomas and hemangioblastomas) and seven secondary tumors evolved from a low grade glioma, thus providing a mixed sample.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p><jats:italic><jats:styled-content style=\"fixed-case\">IDH<\/jats:styled-content>1<\/jats:italic><jats:sup><jats:italic>R132H<\/jats:italic><\/jats:sup> gene mutation was found in 12 patients (15%) and appears more frequently in secondary tumors (5 (71.4%) whereas in 7 (9.7%) primary tumors (<jats:italic>p<\/jats:italic>\u00a0&lt;\u00a0.001)). The mutation is related to <jats:styled-content style=\"fixed-case\">WHO<\/jats:styled-content> grade <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content> in primary tumors and a supratentorial location in secondary tumors. The <jats:styled-content style=\"fixed-case\">OS<\/jats:styled-content> analysis for <jats:italic><jats:styled-content style=\"fixed-case\">IDH<\/jats:styled-content>1<\/jats:italic> showed a tendency towards a better prognosis of the tumors containing the mutation (<jats:italic>p<\/jats:italic>\u00a0=\u00a0.059).The <jats:italic><jats:styled-content style=\"fixed-case\">IDH<\/jats:styled-content>1<\/jats:italic><jats:sup><jats:italic>R132H<\/jats:italic><\/jats:sup> mutation confers a better <jats:styled-content style=\"fixed-case\">PFS<\/jats:styled-content> (<jats:italic>p<\/jats:italic>\u00a0=\u00a0.025) on primary tumors. The T allele of <jats:italic><jats:styled-content style=\"fixed-case\">VEFG<\/jats:styled-content><\/jats:italic> +936 C\/T polymorphism was found in 16 patients (20%). No relation was found between this polymorphism and primary or secondary tumor, neither with <jats:styled-content style=\"fixed-case\">OS<\/jats:styled-content> or <jats:styled-content style=\"fixed-case\">PFS<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p><jats:italic><jats:styled-content style=\"fixed-case\">IDH<\/jats:styled-content>1<\/jats:italic><jats:sup><jats:italic>R132H<\/jats:italic><\/jats:sup> gene mutation is exclusive in supratentorial tumors and more frequent in secondary ones, with a greater survival trend and better <jats:styled-content style=\"fixed-case\">PFS<\/jats:styled-content> in patients who carry it. The T allele of <jats:italic><jats:styled-content style=\"fixed-case\">VEGF<\/jats:styled-content><\/jats:italic> +936 C\/T polymorphism is more common in primary tumors, although there is no statistical relation with survival.<\/jats:p><\/jats:sec>","DOI":"10.1002\/brb3.718","type":"journal-article","created":{"date-parts":[[2017,8,2]],"date-time":"2017-08-02T09:34:55Z","timestamp":1501666495000},"source":"Crossref","is-referenced-by-count":7,"title":["Genetic alterations of <scp>IDH<\/scp>1 and Vegf in brain tumors"],"prefix":"10.1002","volume":"7","author":[{"given":"Silvia","family":"Veganzones","sequence":"first","affiliation":[{"name":"Department of Clinical Analysis Hospital Cl\u00ednico San Carlos and Hospital Universitario Puerta de Hierro\u2010Majadahonda  Majadahonda Madrid Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Virginia","family":"de la Orden","sequence":"additional","affiliation":[{"name":"Department of Clinical Analysis Hospital 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