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Comparative analysis of molecular and histological glioblastomas: insights into prognostic variance

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dc.contributor.author김세훈-
dc.contributor.author박예원-
dc.contributor.author신나영-
dc.contributor.author안성수-
dc.contributor.author윤홍인-
dc.contributor.author이승구-
dc.contributor.author장종희-
dc.contributor.author최서희-
dc.contributor.author한경화-
dc.date.accessioned2024-12-06T02:13:52Z-
dc.date.available2024-12-06T02:13:52Z-
dc.date.issued2024-09-
dc.identifier.issn0167-594X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/200728-
dc.description.abstractPurposeWhether molecular glioblastomas (GBMs) identify with a similar dismal prognosis as a &quot;classical&quot; histological GBM is controversial. This study aimed to compare the clinical, molecular, imaging, surgical factors, and prognosis between molecular GBMs and histological GBMs. MethodsRetrospective chart and imaging review was performed in 983 IDH-wildtype GBM patients (52 molecular GBMs and 931 histological GBMs) from a single institution between 2005 and 2023. Propensity score-matched analysis was additionally performed to adjust for differences in baseline variables between molecular GBMs and histological GBMs. ResultsMolecular GBM patients were substantially younger (58.1 vs. 62.4, P = 0.014) with higher rate of TERTp mutation (84.6% vs. 50.3%, P < 0.001) compared with histological GBM patients. Imaging showed higher incidence of gliomatosis cerebri pattern (32.7% vs. 9.2%, P < 0.001) in molecular GBM compared with histological GBM, which resulted in lesser extent of resection (P < 0.001) in these patients. The survival was significantly better in molecular GBM compared to histological GBM (median OS 30.2 vs. 18.4 months, P = 0.001). The superior outcome was confirmed in propensity score analyses by matching histological GBM to molecular GBM (P < 0.001). ConclusionThere are distinct clinical, molecular, and imaging differences between molecular GBMs and histological GBMs. Our results suggest that molecular GBMs have a more favorable prognosis than histological GBMs.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherSpringer-
dc.relation.isPartOfJOURNAL OF NEURO-ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHBrain Neoplasms* / diagnostic imaging-
dc.subject.MESHBrain Neoplasms* / genetics-
dc.subject.MESHBrain Neoplasms* / mortality-
dc.subject.MESHBrain Neoplasms* / pathology-
dc.subject.MESHFemale-
dc.subject.MESHGlioblastoma* / diagnostic imaging-
dc.subject.MESHGlioblastoma* / genetics-
dc.subject.MESHGlioblastoma* / pathology-
dc.subject.MESHHumans-
dc.subject.MESHIsocitrate Dehydrogenase / genetics-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMutation*-
dc.subject.MESHPrognosis-
dc.subject.MESHRetrospective Studies-
dc.titleComparative analysis of molecular and histological glioblastomas: insights into prognostic variance-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학교실)-
dc.contributor.googleauthorMyunghwan Lee-
dc.contributor.googleauthorPhilipp Karschnia-
dc.contributor.googleauthorYae Won Park-
dc.contributor.googleauthorKaeum Choi-
dc.contributor.googleauthorKyunghwa Han-
dc.contributor.googleauthorSeo Hee Choi-
dc.contributor.googleauthorHong In Yoon-
dc.contributor.googleauthorNa-Young Shin-
dc.contributor.googleauthorSung Soo Ahn-
dc.contributor.googleauthorJoerg-Christian Tonn-
dc.contributor.googleauthorJong Hee Chang-
dc.contributor.googleauthorSe Hoon Kim-
dc.contributor.googleauthorSeung-Koo Lee-
dc.identifier.doi10.1007/s11060-024-04737-9-
dc.contributor.localIdA00610-
dc.contributor.localIdA05330-
dc.contributor.localIdA02089-
dc.contributor.localIdA02234-
dc.contributor.localIdA04777-
dc.contributor.localIdA02912-
dc.contributor.localIdA03470-
dc.contributor.localIdA04867-
dc.contributor.localIdA04267-
dc.relation.journalcodeJ01629-
dc.identifier.eissn1573-7373-
dc.identifier.pmid39115615-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s11060-024-04737-9-
dc.subject.keywordGlioblastoma-
dc.subject.keywordGlioma-
dc.subject.keywordSurvival-
dc.subject.keywordWorld health organization-
dc.contributor.alternativeNameKim, Se Hoon-
dc.contributor.affiliatedAuthor김세훈-
dc.contributor.affiliatedAuthor박예원-
dc.contributor.affiliatedAuthor신나영-
dc.contributor.affiliatedAuthor안성수-
dc.contributor.affiliatedAuthor윤홍인-
dc.contributor.affiliatedAuthor이승구-
dc.contributor.affiliatedAuthor장종희-
dc.contributor.affiliatedAuthor최서희-
dc.contributor.affiliatedAuthor한경화-
dc.citation.volume169-
dc.citation.number3-
dc.citation.startPage531-
dc.citation.endPage541-
dc.identifier.bibliographicCitationJOURNAL OF NEURO-ONCOLOGY, Vol.169(3) : 531-541, 2024-09-
Appears in Collections:
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
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers

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