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

Authors
 Myunghwan Lee  ;  Philipp Karschnia  ;  Yae Won Park  ;  Kaeum Choi  ;  Kyunghwa Han  ;  Seo Hee Choi  ;  Hong In Yoon  ;  Na-Young Shin  ;  Sung Soo Ahn  ;  Joerg-Christian Tonn  ;  Jong Hee Chang  ;  Se Hoon Kim  ;  Seung-Koo Lee 
Citation
 JOURNAL OF NEURO-ONCOLOGY, Vol.169(3) : 531-541, 2024-09 
Journal Title
JOURNAL OF NEURO-ONCOLOGY
ISSN
 0167-594X 
Issue Date
2024-09
MeSH
Adult ; Aged ; Brain Neoplasms* / diagnostic imaging ; Brain Neoplasms* / genetics ; Brain Neoplasms* / mortality ; Brain Neoplasms* / pathology ; Female ; Glioblastoma* / diagnostic imaging ; Glioblastoma* / genetics ; Glioblastoma* / pathology ; Humans ; Isocitrate Dehydrogenase / genetics ; Male ; Middle Aged ; Mutation* ; Prognosis ; Retrospective Studies
Keywords
Glioblastoma ; Glioma ; Survival ; World health organization
Abstract
PurposeWhether molecular glioblastomas (GBMs) identify with a similar dismal prognosis as a "classical" 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.
Full Text
https://link.springer.com/article/10.1007/s11060-024-04737-9
DOI
10.1007/s11060-024-04737-9
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
Yonsei Authors
Kim, Se Hoon(김세훈) ORCID logo https://orcid.org/0000-0001-7516-7372
Park, Yae Won(박예원) ORCID logo https://orcid.org/0000-0001-8907-5401
Shin, Na Young(신나영)
Ahn, Sung Soo(안성수) ORCID logo https://orcid.org/0000-0002-0503-5558
Yoon, Hong In(윤홍인) ORCID logo https://orcid.org/0000-0002-2106-6856
Lee, Seung Koo(이승구) ORCID logo https://orcid.org/0000-0001-5646-4072
Chang, Jong Hee(장종희) ORCID logo https://orcid.org/0000-0003-1509-9800
Choi, Seo Hee(최서희) ORCID logo https://orcid.org/0000-0002-4083-6414
Han, Kyung Hwa(한경화)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200728
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