2020
DOI: 10.1007/s11910-020-01040-8
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Lower Grade Gliomas

Abstract: Purpose of Review Low-grade gliomas (LGG) are a group of primary brain tumors that arise from supporting glial cells. They are characterized by a mutation in the isocitrate dehydrogenase (IDH) enzyme and include astrocytomas and oligodendrogliomas. They usually affect young adults, and their main treatment consists of surgical resection, followed by radiation and chemotherapy in selected patients. This article reviews recent research on the clinical and molecular aspects of the disease and innovative therapeut… Show more

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Cited by 95 publications
(81 citation statements)
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“…Despite recent significant advances in treatment and diagnosis of LGG, most LGG patients have poor prognosis [46] . Although neoadjuvant immune checkpoint blockade (ICB) therapy improves overall prognosis of patients, immunotherapy for gliomas is now in clinical trials with slow progress [47] , [48] , [49] .…”
Section: Discussionmentioning
confidence: 99%
“…Despite recent significant advances in treatment and diagnosis of LGG, most LGG patients have poor prognosis [46] . Although neoadjuvant immune checkpoint blockade (ICB) therapy improves overall prognosis of patients, immunotherapy for gliomas is now in clinical trials with slow progress [47] , [48] , [49] .…”
Section: Discussionmentioning
confidence: 99%
“…With the exception of grade I glioma, these tumors invariably progress intracranially, despite all available treatment modalities, leading to disability and death. Life expectancy depends on tumor grade and molecular features, ranging from a median of 14.6 months in glioblastoma (GBM) after surgery, radiation therapy, and temozolomide chemotherapy to a median of more than 15 years in grade II oligodendroglioma with a favorable molecular profile (i.e., 1p/19q co-deletion) and clinical features (age, neurological conditions, tumor size) [ 1 , 2 ].…”
Section: Introductionmentioning
confidence: 99%
“…Diffuse low-grade gliomas or World Health Organisation grade II gliomas (LGG) represents a group of tumours developed from oligodendrocyte and astrocytic precursors, with a slow and continuously growth pattern, infiltrative character, usually along white matter tracts and progression towards a malignant histological type. Traditionally this includes diffuse astrocytoma, oligodendroglioma and oligoastrocytoma [35,66].…”
Section: Natural History and The New Molecular Classificationmentioning
confidence: 99%