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High Radiation Dose to the Fornix Causes Symptomatic Radiation Necrosis in Patients with Anaplastic Oligodendroglioma

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dc.contributor.author강석구-
dc.contributor.author문주형-
dc.contributor.author박예원-
dc.contributor.author윤홍인-
dc.contributor.author장종희-
dc.contributor.author조재호-
dc.contributor.author김태형-
dc.date.accessioned2024-03-22T07:02:59Z-
dc.date.available2024-03-22T07:02:59Z-
dc.date.issued2024-01-
dc.identifier.issn0513-5796-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198671-
dc.description.abstractPurpose: Surgery, radiotherapy (RT), and chemotherapy have prolonged the survival of patients with anaplastic oligodendroglio ma. However, whether RT induces long-term toxicity remains unknown. We analyzed the relationship between the RT dose to the fornix and symptomatic radiation necrosis (SRN). Materials and Methods: A total of 67 patients treated between 2009 and 2019 were analyzed. SRN was defined according to the following three criteria: 1) radiographic findings, 2) symptoms attributable to the lesion, and 3) treatment resulting in symptom improvement. Various contours, including the fornix, were delineated. Univariate and multivariate analyses of the relationship between RT dose and SRN, as well as receiver operating characteristic curve analysis for cut-off values, were performed. Results: The most common location was the frontal lobe (n=40, 60%). Gross total resection was performed in 38 patients (57%), and 42 patients (63%) received procarbazine, lomustine, and vincristine chemotherapy. With a median follow-up of 42 months, the me dian overall and progression-free survival was 74 months. Sixteen patients (24%) developed SRN. In multivariate analysis, age and maximum dose to the fornix were associated with the development of SRN. The cut-off values for the maximum dose to the fornix and age were 59 Gy (equivalent dose delivered in 2 Gy fractions) and 46 years, respectively. The rate of SRN was higher in patients whose maximum dose to the fornix was >59 Gy (13% vs. 43%, p=0.005). Conclusion: The maximum dose to the fornix was a significant factor for SRN development. While fornix sparing may help main tain neurocognitive function, additional studies are needed.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherYonsei University-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols / adverse effects-
dc.subject.MESHBrain Neoplasms* / drug therapy-
dc.subject.MESHBrain Neoplasms* / pathology-
dc.subject.MESHBrain Neoplasms* / radiotherapy-
dc.subject.MESHHumans-
dc.subject.MESHNecrosis / chemically induced-
dc.subject.MESHNecrosis / drug therapy-
dc.subject.MESHOligodendroglioma* / drug therapy-
dc.subject.MESHOligodendroglioma* / radiotherapy-
dc.subject.MESHRadiation Dosage-
dc.subject.MESHVincristine / adverse effects-
dc.titleHigh Radiation Dose to the Fornix Causes Symptomatic Radiation Necrosis in Patients with Anaplastic Oligodendroglioma-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurosurgery (신경외과학교실)-
dc.contributor.googleauthorTae Hyung Kim-
dc.contributor.googleauthorJaeho Cho-
dc.contributor.googleauthorSeok-Gu Kang-
dc.contributor.googleauthorJu Hyung Moon-
dc.contributor.googleauthorChang-Ok Suh-
dc.contributor.googleauthorYae Won Park-
dc.contributor.googleauthorJong Hee Chang-
dc.contributor.googleauthorHong In Yoon-
dc.identifier.doi10.3349/ymj.2023.0112-
dc.contributor.localIdA00036-
dc.contributor.localIdA01383-
dc.contributor.localIdA05330-
dc.contributor.localIdA04777-
dc.contributor.localIdA03470-
dc.contributor.localIdA03901-
dc.relation.journalcodeJ02813-
dc.identifier.eissn1976-2437-
dc.identifier.pmid38154474-
dc.subject.keywordAnaplastic oligodendroglioma-
dc.subject.keywordcognitive function-
dc.subject.keywordfornix-
dc.subject.keywordradiation necrosis-
dc.subject.keywordradiotherapy-
dc.contributor.alternativeNameKang, Seok Gu-
dc.contributor.affiliatedAuthor강석구-
dc.contributor.affiliatedAuthor문주형-
dc.contributor.affiliatedAuthor박예원-
dc.contributor.affiliatedAuthor윤홍인-
dc.contributor.affiliatedAuthor장종희-
dc.contributor.affiliatedAuthor조재호-
dc.citation.volume65-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage9-
dc.identifier.bibliographicCitationYONSEI MEDICAL JOURNAL, Vol.65(1) : 1-9, 2024-01-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurosurgery (신경외과학교실) > 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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