Unique genetic and epigenetic mechanisms driving paediatric diffuse high-grade glioma

C Jones, SJ Baker - Nature Reviews Cancer, 2014 - nature.com
Diffuse high-grade gliomas (HGGs) of childhood are a devastating spectrum of disease with
no effective cures. The two-year survival for paediatric HGG ranges from 30%, for tumours …

Consensus on the management of intracranial germ-cell tumours

MJ Murray, U Bartels, R Nishikawa… - The Lancet …, 2015 - thelancet.com
The management of intracranial germ-cell tumours is complex because of varied clinical
presentations, tumour sites, treatments and outcomes, and the need for multidisciplinary …

Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma

H Nikbakht, E Panditharatna, LG Mikael, R Li… - Nature …, 2016 - nature.com
Abstract Diffuse Intrinsic Pontine Gliomas (DIPGs) are deadly paediatric brain tumours
where needle biopsies help guide diagnosis and targeted therapies. To address spatial …

Detection of Histone H3 mutations in cerebrospinal fluid-derived tumor DNA from children with diffuse midline glioma

TY Huang, A Piunti, RR Lulla, J Qi… - Acta neuropathologica …, 2017 - Springer
Diffuse midline gliomas (including diffuse intrinsic pontine glioma, DIPG) are highly morbid
glial neoplasms of the thalamus or brainstem that typically arise in young children and are …

Response assessment in diffuse intrinsic pontine glioma: recommendations from the Response Assessment in Pediatric Neuro-Oncology (RAPNO) working group

TM Cooney, KJ Cohen, CV Guimaraes, G Dhall… - The Lancet …, 2020 - thelancet.com
Optimising the conduct of clinical trials for diffuse intrinsic pontine glioma involves use of
consistent, objective disease assessments and standardised response criteria. The …

Pediatric brain tumor genetics: what radiologists need to know

J AlRayahi, M Zapotocky, V Ramaswamy… - Radiographics, 2018 - pubs.rsna.org
Brain tumors are the most common solid tumors in the pediatric population. Pediatric neuro-
oncology has changed tremendously during the past decade owing to ongoing genomic …

Diffuse intrinsic pontine glioma: new pathophysiological insights and emerging therapeutic targets

T B. Johung, M Monje - Current Neuropharmacology, 2017 - benthamdirect.com
Background: Diffuse Intrinsic Pontine Glioma (DIPG) is the leading cause of brain tumor-
related death in children, with median survival of less than one year. Despite decades of …

A phase II study of continuous oral mTOR inhibitor everolimus for recurrent, radiographic-progressive neurofibromatosis type 1–associated pediatric low-grade glioma …

NJ Ullrich, SP Prabhu, AT Reddy, MJ Fisher… - Neuro …, 2020 - academic.oup.com
Background Activation of the mammalian target of rapamycin (mTOR) pathway is observed
in neurofibromatosis type 1 (NF1) associated low-grade gliomas (LGGs), but agents that …

[HTML][HTML] Pediatric low-grade glioma: Targeted therapeutics and clinical trials in the molecular era

N Manoharan, KX Liu, S Mueller, DA Haas-Kogan… - Neoplasia, 2023 - Elsevier
Abstract pLGGs are a group of tumors for which the era of molecular diagnostics has truly
shifted treatment paradigms and patient care. The discovery that this group of tumors is …

Diffuse intrinsic pontine glioma: a reassessment

NJ Robison, MW Kieran - Journal of neuro-oncology, 2014 - Springer
Diffuse intrinsic pontine glioma (DIPG) is a disease of childhood whose abysmal prognosis
has remained unchanged for over 50 years. Biologic investigation has been stymied by lack …