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The Korean Society for Neuro-Oncology (KSNO) Guideline for WHO Grade II Cerebral Gliomas in Adults: Version 2019.01open access

Authors
김영준김재용위찬우Tae Hoon RohJe Beom HongHyuk-Jin OhSeok-Gu KangShin Hyuk KangDoo-Sik KongSung Hwan KimSe-Hyuk KimSe-Hoon Kim김유정Eui Hyun Kim김인아Ho Sung KimJae-Sung ParkHyun Jin ParkSang Woo SongKyoung-Su SungSeung Ho YangWan-Soo Yoon윤홍인이지혜이순태Sea-Won LeeYoun Soo LeeJae Joon LimJong Hee ChangTae-Young Jung정혜림Jae Ho Cho최승홍Hyoung Soo Choi임도훈정동섭
Issue Date
2019
Publisher
대한뇌종양학회
Keywords
Korean Society for Neuro-Oncology; Guideline; Grade II Gliomas; Practice
Citation
Brain Tumor Research and Treatment, v.7, no.2, pp 74 - 84
Pages
11
Indexed
KCI
Journal Title
Brain Tumor Research and Treatment
Volume
7
Number
2
Start Page
74
End Page
84
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/28879
DOI
10.14791/btrt.2019.7.e43
ISSN
2288-2405
2288-2413
Abstract
Background: There was no practical guideline for the management of patients with central nervous system tumor in Korea for many years. Thus, the Korean Society for Neuro-Oncology (KSNO), a multidisciplinary academic society, has developed the guideline for glioblastoma. Subsequently, the KSNO guideline for World Health Organization (WHO) grade II cerebral glioma in adults is established. Methods: The Working Group was composed of 35 multidisciplinary medical experts in Korea. References were identified by searching PubMed, MEDLINE, EMBASE, and Cochrane CENTRAL databases using specific and sensitive keywords as well as combinations of keywords regarding diffuse astrocytoma and oligodendroglioma of brain in adults. Results: Whenever radiological feature suggests lower grade glioma, the maximal safe resection if feasible is recommended globally. After molecular and histological examinations, patients with diffuse astrocytoma, isocitrate dehydrogenase (IDH)-wildtype without molecular feature of glioblastoma should be primarily treated by standard brain radiotherapy and adjuvant temozolomide chemotherapy (Level III) while those with molecular feature of glioblastoma should be treated following the protocol for glioblastomas. In terms of patients with diffuse astrocytoma, IDH-mutant and oligodendroglioma (IDH-mutant and 1p19q codeletion), standard brain radiotherapy and adjuvant PCV (procarbazine+lomustine+vincristine) combination chemotherapy should be considered primarily for the high-risk group while observation with regular follow up should be considered for the low-risk group. Conclusion: The KSNO's guideline recommends that WHO grade II gliomas should be treated by maximal safe resection, if feasible, followed by radiotherapy and/or chemotherapy according to molecular and histological features of tumors and clinical characteristics of patients.
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Ansan Hospital (Department of Neurosurgery, Ansan Hospital)
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