2021
DOI: 10.1007/s00381-021-05138-3
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Targeted therapy for pediatric low-grade glioma

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Cited by 14 publications
(8 citation statements)
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“…For instance, the identification of BRAF V600E mutations allows targeted disruption by using BRAF inhibitors, with favorable clinical results. 22 The diagnosis of high-grade astrocytoma with piloid features recognizes unusual cases in which a relatively circumscribed tumor with distinct piloid cytology occurs in the setting of a more malignant astrocytoma (WHO grades 3 or 4). 23 These tumors usually occur in adults, exhibit CDKN2A/B deletions, and have a distinct DNA methylation profile that differs from the typical childhood pilocytic astrocytomas.…”
Section: Gliomasmentioning
confidence: 99%
“…For instance, the identification of BRAF V600E mutations allows targeted disruption by using BRAF inhibitors, with favorable clinical results. 22 The diagnosis of high-grade astrocytoma with piloid features recognizes unusual cases in which a relatively circumscribed tumor with distinct piloid cytology occurs in the setting of a more malignant astrocytoma (WHO grades 3 or 4). 23 These tumors usually occur in adults, exhibit CDKN2A/B deletions, and have a distinct DNA methylation profile that differs from the typical childhood pilocytic astrocytomas.…”
Section: Gliomasmentioning
confidence: 99%
“…Most pediatric low-grade gliomas, as a further example, are defined by alterations in the mitogen activated protein kinase (MAPK) pathway [22]. The detection of these alterations has led to the development of targeted therapies, directed against these kinases, for example, MEK and BRAF inhibitors [23][24][25]. The efficacy and safety of these agents, for example, dabrafenib or trametinib, are currently being evaluated in clinical trials and may have the potential to replace conventional chemotherapy as a standard of care for pediatric low-grade gliomas [26,27].…”
Section: Treatment Modalities and Related Long-term Issues In Pediatr...mentioning
confidence: 99%
“…Many of the targeted agents, which have been proven to be effective in early-phase pediatric brain tumor trials (eg, vemurafenib, dabrafenib, bevacizumab, and trametinib), have been licensed for use in adults in many countries. 12 , 13 Even in some MICs where these drugs are available, the high cost continues to be a major hurdle for widespread use of these therapies. Moreover, these drugs need to be given for a long period of time, and the majority of studies have shown the duration of therapy to be over 1 year, which leads to a long-term problem with accessibility and affordability.…”
Section: Drug Access In Lmicsmentioning
confidence: 99%