{"id":13926,"date":"2024-10-04T11:41:35","date_gmt":"2024-10-04T11:41:35","guid":{"rendered":"https:\/\/genekor.com\/2024\/10\/04\/fra-new-assay-pathology-lab\/"},"modified":"2025-04-10T13:02:04","modified_gmt":"2025-04-10T13:02:04","slug":"fra-new-assay-pathology-lab","status":"publish","type":"post","link":"https:\/\/genekor.com\/et\/2024\/10\/04\/fra-new-assay-pathology-lab\/","title":{"rendered":"FR\u03b1: uus test Genekor Patoloogialaboris munasarjav\u00e4hi sihtm\u00e4rkraviks"},"content":{"rendered":"\n<p>FR\u03b1 test on vajalik mirvetuksimab-soravtansiini ravi m\u00e4\u00e4ramiseks, mis on suunatud plaatina-resistentse munasarjav\u00e4higa patsientidele, kes on FR\u03b1-positiivsed ja saanud juba eelnevalt 1-3 liini ravi.<\/p>\n\n\n\n<p>19. septembril 2024 andis Euroopa Ravimiamet (EMA) MIRASOL III faasi uuringu p\u00f5hjal positiivse hinnangu mirvetuksimab-soravtansiini ravi m\u00e4\u00e4ramiseks FR\u03b1-positiivse plaatina-resistentse munasarjav\u00e4higa patsientidele, kes on juba saanud 1-3 liini ravi.<\/p>\n\n\n\n<p>USA-s on mirvetuksimab-soravtansiin FDA poolt heaks kiidetud alates 2024. aasta m\u00e4rtsist.<\/p>\n\n\n\n<p>FOLR1 (FR\u03b1) ekspressiooni m\u00e4\u00e4ramine toimub meie laboris, kasutades<strong> FDA poolt<\/strong> <strong>heaks kiidetud Ventana\u00ae FOLR1 (FOLR1-2.1) RxDx Assay<\/strong> (Ventana Medical Systems, Inc.).<\/p>\n\n\n\n<p>Kasutame Ventana BenchMark Ultra automatiseeritud platvormi.<\/p>\n\n\n\n<p>Kliinilises praktikas loetakse proovi FOLR1 (FR\u03b1) positiivseks, kui neoplastilistel rakkudel on m\u00f5\u00f5dukas (2+) kuni intensiivne (3+) t\u00e4ielik v\u00f5i mittet\u00e4ielik membraani v\u00e4rvumine 75% v\u00f5i enamal proovist.<\/p>\n\n\n\n<p>Proov on vastuv\u00f5etav, kui see sisaldab v\u00e4hemalt sada eluj\u00f5ulist v\u00e4hirakku. Kasutatakse positiivset v\u00e4list kontrolli.<\/p>\n\n\n\n<p>Vaata EMA positiivset arvamust<\/p>\n\n\n\n<p>Genekori kogenud ja spetsialiseerunud t\u00f6\u00f6tajad on siin selleks, et pakkuda arstidele k\u00f5ige usaldusv\u00e4\u00e4rsemaid ja t\u00e4psemaid tulemusi, toetades j\u00f5upingutusi pakkuda patsientidele parimat v\u00f5imalikku abi.<\/p>\n\n\n\n<p>Vaadake Genekori Patoloogialaboris tehtud teste.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>FR\u03b1 test on vajalik mirvetuksimab-soravtansiini ravi m\u00e4\u00e4ramiseks, mis on suunatud plaatina-resistentse munasarjav\u00e4higa patsientidele, kes on FR\u03b1-positiivsed ja saanud juba eelnevalt 1-3 liini ravi. 19. septembril 2024 andis Euroopa Ravimiamet (EMA) [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":12956,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[121,94],"tags":[],"class_list":["post-13926","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news-et","category-uncategorized-et"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v24.0 (Yoast SEO v24.0) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>FRa \u03b5\u03be\u03ad\u03c4\u03b1\u03c3\u03b7 \u03b3\u03b9\u03b1 \u03c3\u03c4\u03bf\u03c7\u03b5\u03cd\u03bf\u03c5\u03c3\u03b1 \u03b8\u03b5\u03c1\u03b1\u03c0\u03b5\u03af\u03b1 \u03c4\u03bf\u03c5 \u03ba\u03b1\u03c1\u03ba\u03af\u03bd\u03bf\u03c5 \u03c4\u03c9\u03bd \u03bf\u03c9\u03b8\u03b7\u03ba\u03ce\u03bd - Genekor<\/title>\n<meta name=\"description\" content=\"\u03a3\u03c4\u03bf 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