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Title:Analiza trenda napotitev na onkološko genetsko obravnavo pri bolnicah z rakom jajčnikov, ki potrebujejo genetski izvid za načrtovanje zdravljenja in predstavitev novih kliničnih poti obravnave
Authors:Novak, Svetlana (Author)
Hotujec, Simona (Author)
Strojnik, Ksenija (Author)
Blatnik, Ana (Author)
Škof, Erik (Author)
Ravnik-Oblak, Maja (Author)
Novaković, Srdjan (Author)
Krajc, Mateja (Author)
Language:Slovenian
Tipology:1.01 - Original Scientific Article
Organisation:Logo OI - Institute of Oncology
Abstract:Zadnjih nekaj let se v genetskih ambulantah soočamo s pogostejšimi napotitvami bolnikov z rakom na genetsko obravnavo. Izvid genetskega testiranja je namreč pri bolnicah z epitelijskim nemucinoznim rakom jajčnikov/jajcevodov/primarnim peritonealnim seroznim karcinomom (PPSC) in bolnikih z metastatskim rakom prostate/pankreasa/dojk lahko zelo pomemben za načrtovanje zdravljenja z zaviralci poli(ADP-riboza)-polimeraze (PARP). Ker se z obravnavo običajno mudi, smo izdelali dve klinični poti, ki omogočita tem bolnikom prednostno obravnavo.
Keywords:epitelijski nemucinozni rak jajčnikov, epitelijski nemucinozni rak jajcevodov, primarni peritonealni serozni karcinom/PPSC, prednostna napotitev, genetsko testiranje, BRCA1/2
Year of publishing:2021
Publisher:Onkološki inštitut Ljubljana
COBISS_ID:88595971 Link is opened in a new window
UDC:616-07
ISSN on article:1408-1741
DOI:10.25670/oi2021-012on Link is opened in a new window
Views:268
Downloads:139
Files:.pdf PDF - Presentation file, download (416,01 KB)
URL URL - Source URL, visit https://www.onko-i.si/onkologija/arhiv-revije/letnik-xxv-st-2
 
Journal:Onkologija
Onkološki inštitut
 
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License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:01.12.2021

Secondary language

Language:English
Title:Analysis of the referral trend in ovarian cancer patients who need genetic assessment for treatment planning and presentation of new clinical pathways


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