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최승원

Choi, Seung-Won
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dc.citation.endPage 579 -
dc.citation.number 3 -
dc.citation.startPage 571 -
dc.citation.title JOURNAL OF NEURO-ONCOLOGY -
dc.citation.volume 145 -
dc.contributor.author Choi, Seung-Won -
dc.contributor.author Cho, Kyung Rae -
dc.contributor.author Choi, Jung Won -
dc.contributor.author Kong, Doo-Sik -
dc.contributor.author Seol, Ho Jun -
dc.contributor.author Nam, Do-Hyun -
dc.contributor.author Lee, Jung-Il -
dc.date.accessioned 2025-11-26T10:58:13Z -
dc.date.available 2025-11-26T10:58:13Z -
dc.date.created 2025-10-14 -
dc.date.issued 2019-12 -
dc.description.abstract Purpose Stereotactic radiosurgery (SRS) is feasible for malignant glioma; however, delivering the optimal radiation dose with sufficient large-volume coverage is a major concern. We aimed to investigate the clinical efficacy and safety of fractionated SRS (fSRS) versus single-session SRS (sSRS) for malignant gliomas. Methods We retrospectively reviewed 58 malignant glioma patients who underwent gamma knife SRS from January 2015 to December 2018. Forty-one underwent sSRS, and 17 underwent fSRS. Median dose for fSRS was 28 Gy (range 24-35 Gy), with a median dose of 6 Gy per fraction (range 5-7 Gy). Patients received 4 or 5 fractions on consecutive days. Median dose for sSRS was 18 Gy (range 11-25 Gy), with a median isodose of 50% (range 50-65%). Mean target volumes were 5.9 and 19.3 cc for sSRS and fSRS, respectively (p < 0.001, two-sided t test). Results After SRS, median progression-free survival (PFS) was 4.5 and 4.6 months (p = 0.58), and median overall survival (OS) was 12.7 and 12.6 months for sSRS and fSRS (p = 0.41), respectively (log-rank test). The incidence of clinically significant radiation necrosis was 20.5% (8/39) and 18.8% (3/16) for sSRS and fSRS, respectively (p = 1, Fisher's exact test). Conclusion fSRS for malignant glioma conferred local control and survival comparable with conventional sSRS. The radiation necrosis incidence was comparable between groups when a parallel biological effective dose was administered to the larger target volumes in the fSRS group. fSRS can be a better alternative to sSRS if re-irradiation is considered for large malignant gliomas. -
dc.identifier.bibliographicCitation JOURNAL OF NEURO-ONCOLOGY, v.145, no.3, pp.571 - 579 -
dc.identifier.doi 10.1007/s11060-019-03328-3 -
dc.identifier.issn 0167-594X -
dc.identifier.scopusid 2-s2.0-85075121148 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/88599 -
dc.identifier.wosid 000495213100001 -
dc.language 영어 -
dc.publisher SPRINGER -
dc.title Fractionated stereotactic radiosurgery for malignant gliomas: comparison with single session stereotactic radiosurgery -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Oncology; Clinical Neurology -
dc.relation.journalResearchArea Oncology; Neurosciences & Neurology -
dc.type.docType Article -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Stereotactic radiosurgery -
dc.subject.keywordAuthor Fractionated stereotactic radiosurgery -
dc.subject.keywordAuthor High-grade glioma -
dc.subject.keywordPlus BRAIN METASTASES -
dc.subject.keywordPlus RADIOTHERAPY -
dc.subject.keywordPlus ADJUVANT -
dc.subject.keywordPlus EFFICACY -
dc.subject.keywordPlus TEMOZOLOMIDE -
dc.subject.keywordPlus BEVACIZUMAB -
dc.subject.keywordPlus CONCOMITANT -
dc.subject.keywordPlus RECURRENCE -
dc.subject.keywordPlus TUMORS -
dc.subject.keywordPlus GLIOBLASTOMA-MULTIFORME -

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