483 627

Cited 36 times in

Extent of resection and molecular pathologic subtype are potent prognostic factors of adult WHO grade II glioma

DC Field Value Language
dc.contributor.author강석구-
dc.contributor.author김세훈-
dc.contributor.author서창옥-
dc.contributor.author윤홍인-
dc.contributor.author장종희-
dc.contributor.author조재호-
dc.contributor.author최진현-
dc.contributor.author최혜진-
dc.date.accessioned2020-02-26T06:53:13Z-
dc.date.available2020-02-26T06:53:13Z-
dc.date.issued2020-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/175328-
dc.description.abstractWe evaluated prognostic factors of adult low-grade glioma (LGG) according to the new 2016 WHO classification. Records of 153 patients diagnosed with WHO grade II LGG between 2003 and 2015 were retrospectively reviewed. Based on the 2016 WHO classification, 80 patients (52.3%) had diffuse astrocytoma, IDH-mutant; 45 (29.4%) had oligodendroglioma, IDH-mutant and 1p/19q-codeleted (ODG); and 28 (18.3%) had diffuse astrocytoma, IDH-wildtype. Gross total resection (GTR) was performed in 71 patients (46.4%), subtotal resection in 31 (20.3%), partial resection in 43 (28.1%), and biopsy in 8 (5.2%). One hundred two patients (66.7%) received postoperative radiotherapy. The 5- and 10-year progression-free survival (PFS) rates were 72.7% and 51.5%, respectively, and the 5- and 10-year overall survival (OS) rates were 82.5% and 63.5%, respectively. GTR and IDH-mutant and/or 1p/19q codeletion were favorable prognostic factors for PFS and OS. Patients with IDH-wildtype had significantly decreased OS. Among patients with ODG who underwent GTR, no recurrence was observed after radiotherapy. Patients who underwent non-GTR frequently experienced recurrence after radiotherapy (IDH-mutant: 47.6%, IDH-wildtype: 57.9%). In conclusion, molecular classification of LGG was of prognostic relevance, with IDH-wildtype patients having a particularly poor outcome, regardless of the treatment. Favorable results were observed in patients who underwent GTR.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleExtent of resection and molecular pathologic subtype are potent prognostic factors of adult WHO grade II glioma-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurosurgery (신경외과학교실)-
dc.contributor.googleauthorJinhyun Choi-
dc.contributor.googleauthorSe Hoon Kim-
dc.contributor.googleauthorSung Soo Ahn-
dc.contributor.googleauthorHye Jin Choi-
dc.contributor.googleauthorHong In Yoon-
dc.contributor.googleauthorJae Ho Cho-
dc.contributor.googleauthorTae Hoon Roh-
dc.contributor.googleauthorSeok-Gu Kang-
dc.contributor.googleauthorJong Hee Chang-
dc.contributor.googleauthorChang-Ok Suh-
dc.identifier.doi10.1038/s41598-020-59089-x-
dc.contributor.localIdA00036-
dc.contributor.localIdA00610-
dc.contributor.localIdA01919-
dc.contributor.localIdA04777-
dc.contributor.localIdA03470-
dc.contributor.localIdA03901-
dc.contributor.localIdA04697-
dc.contributor.localIdA04219-
dc.relation.journalcodeJ02646-
dc.identifier.eissn2045-2322-
dc.identifier.pmid32034238-
dc.contributor.alternativeNameKang, Seok Gu-
dc.contributor.affiliatedAuthor강석구-
dc.contributor.affiliatedAuthor김세훈-
dc.contributor.affiliatedAuthor서창옥-
dc.contributor.affiliatedAuthor윤홍인-
dc.contributor.affiliatedAuthor장종희-
dc.contributor.affiliatedAuthor조재호-
dc.contributor.affiliatedAuthor최진현-
dc.contributor.affiliatedAuthor최혜진-
dc.citation.volume10-
dc.citation.number1-
dc.citation.startPage2086-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, Vol.10(1) : 2086, 2020-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Neurosurgery (신경외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.