Molecular profiling and targeted therapy in pediatric gliomas: review and consensus recommendations

Z Miklja, A Pasternak, S Stallard, T Nicolaides… - Neuro …, 2019 - academic.oup.com
As the field of neuro-oncology makes headway in uncovering the key oncogenic drivers in
pediatric glioma, the role of precision diagnostics and therapies continues to rapidly evolve …

Genetic alterations shaping tumor response to anti-EGFR therapies

J Vaquero, A Pavy, E Gonzalez-Sanchez… - Drug Resistance …, 2022 - Elsevier
Abstract The Epidermal Growth Factor Receptor (EGFR) has been targeted through the
development of selective tyrosine kinase inhibitors (TKIs) and monoclonal antibodies (mAb) …

[HTML][HTML] The genomic landscape of TERT promoter wildtype-IDH wildtype glioblastoma

BH Diplas, X He, JA Brosnan-Cashman, H Liu… - Nature …, 2018 - nature.com
The majority of glioblastomas can be classified into molecular subgroups based on
mutations in the TERT promoter (TERTp) and isocitrate dehydrogenase 1 or 2 (IDH). These …

[HTML][HTML] SPI1-mediated MIR222HG transcription promotes proneural-to-mesenchymal transition of glioma stem cells and immunosuppressive polarization of …

Y Fan, Z Gao, J Xu, H Wang, Q Guo, B Li, M Li, H Xu… - Theranostics, 2023 - ncbi.nlm.nih.gov
Background: Glioma stem cells (GSCs) are a key factor in glioblastoma (GBM) development
and treatment resistance. GSCs can be divided into the mesenchymal (MES) and proneural …

[HTML][HTML] Dramatic response of BRAF V600E-mutant epithelioid glioblastoma to combination therapy with BRAF and MEK inhibitor: establishment and xenograft of a …

Y Kanemaru, M Natsumeda, M Okada, R Saito… - Acta Neuropathologica …, 2019 - Springer
Epithelioid glioblastoma is a rare aggressive variant of glioblastoma (GBM) characterized by
a dismal prognosis of about 6 months and frequent leptomeningeal dissemination. A recent …

[HTML][HTML] Sustained response of three pediatric BRAFV600E mutated high-grade gliomas to combined BRAF and MEK inhibitor therapy

SA Toll, HN Tran, J Cotter, AR Judkins, B Tamrazi… - Oncotarget, 2019 - ncbi.nlm.nih.gov
Outcomes for children with high-grade gliomas (HGG) remain dismal despite aggressive
treatment strategies. The use of targeted therapy for BRAF V600E mutated malignancies …

[HTML][HTML] Oligonucleotide therapeutics as a new class of drugs for malignant brain tumors: targeting mRNAs, regulatory RNAs, mutations, combinations, and beyond

AM Krichevsky, EJ Uhlmann - Neurotherapeutics, 2019 - Elsevier
Malignant brain tumors are rapidly progressive and often fatal owing to resistance to
therapies and based on their complex biology, heterogeneity, and isolation from systemic …

Concurrent BRAF/MEK inhibitors in BRAF V600–mutant high-grade primary brain tumors

KC Schreck, A Guajardo, DDM Lin, CG Eberhart… - Journal of the National …, 2018 - jnccn.org
BRAF V600 mutations are being identified in patients with primary brain tumors more often
as molecular testing becomes widely available. Targeted treatment with BRAF inhibitors has …

[HTML][HTML] Advances in targeted therapies for pediatric brain tumors

T Mueller, ASG Stucklin, A Postlmayr, S Metzger… - … Treatment Options in …, 2020 - Springer
Abstract Purpose of Review Over the last years, our understanding of the molecular biology
of pediatric brain tumors has vastly improved. This has led to more narrowly defined …

[HTML][HTML] Dabrafenib treatment in a patient with an epithelioid glioblastoma and BRAF V600E mutation

G Ceccon, JM Werner, V Dunkl, C Tscherpel… - International journal of …, 2018 - mdpi.com
Novel therapeutic targets in malignant glioma patients are urgently needed. Point mutations
of the v-Raf murine sarcoma viral oncogene homolog B (BRAF) gene occur predominantly in …