Atypical teratoid/rhabdoid tumors—current concepts, advances in biology, and potential future therapies

MC Frühwald, JA Biegel, F Bourdeaut… - Neuro …, 2016 - academic.oup.com
Atypical teratoid/rhabdoid tumor (AT/RT) is the most common malignant CNS tumor of
children below 6 months of age. The majority of AT/RTs demonstrate genomic alterations in …

Pediatric brain tumors: innovative genomic information is transforming the diagnostic and clinical landscape

A Gajjar, DC Bowers, MA Karajannis… - Journal of Clinical …, 2015 - ascopubs.org
Pediatric neuro-oncology has undergone an exciting and dramatic transformation during the
past 5 years. This article summarizes data from collaborative group and institutional trials …

Atypical teratoid/rhabdoid tumors are comprised of three epigenetic subgroups with distinct enhancer landscapes

PD Johann, S Erkek, M Zapatka, K Kerl, I Buchhalter… - Cancer cell, 2016 - cell.com
Atypical teratoid/rhabdoid tumor (ATRT) is one of the most common brain tumors in infants.
Although the prognosis of ATRT patients is poor, some patients respond favorably to current …

Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis

J Torchia, D Picard, L Lafay-Cousin… - The lancet …, 2015 - thelancet.com
Background Rhabdoid brain tumours, also called atypical teratoid rhabdoid tumours, are
lethal childhood cancers with characteristic genetic alterations of SMARCB1/hSNF5. Lack of …

Atypical teratoid/rhabdoid tumors: challenges and search for solutions

A Biswas, L Kashyap, A Kakkar, C Sarkar… - Cancer management …, 2016 - Taylor & Francis
Atypical teratoid/rhabdoid tumor (AT/RT) is a highly malignant embryonal central nervous
system tumor commonly affecting children< 3 years of age. It roughly constitutes 1%–2% of …

Improved 6‐year overall survival in AT/RT–results of the registry study Rhabdoid 2007

K Bartelheim, K Nemes, A Seeringer, K Kerl… - Cancer …, 2016 - Wiley Online Library
Atypical teratoid rhabdoid tumors (AT/RT) are characterized by mutations and subsequent
inactivation of SMARCB 1 (INI 1, hSNF 5), a predilection for very young children and an …

Atypical teratoid rhabdoid tumor: molecular insights and translation to novel therapeutics

CL Nesvick, L Lafay-Cousin, A Raghunathan… - Journal of neuro …, 2020 - Springer
Introduction Atypical teratoid rhabdoid tumor (ATRT) is a rare, often lethal brain tumor of
childhood characterized by a complex epigenetic landscape amongst a simple genetic …

Pediatric brain tumors: the era of molecular diagnostics, targeted and immune-based therapeutics, and a focus on long term neurologic sequelae

AS Plant-Fox, K O'Halloran, S Goldman - Current Problems in Cancer, 2021 - Elsevier
Pediatric brain tumors are the second most common malignancy of childhood after acute
leukemia and the number one cause of cancer-related mortality 1. Over the past decade …

Multimodal therapy in children and adolescents with newly diagnosed atypical teratoid rhabdoid tumor: individual pooled data analysis and review of the literature

D Schrey, F Carceller Lechón, G Malietzis… - Journal of neuro …, 2016 - Springer
Atypical teratoid rhabdoid tumour (ATRT) is a malignant tumour of the central nervous
system with a dismal prognosis. There is no consensus on optimal treatment and different …

Atypical teratoid rhabdoid tumor in the first year of life: the Canadian ATRT registry experience and review of the literature

M Fossey, H Li, S Afzal, AS Carret, DD Eisenstat… - Journal of neuro …, 2017 - Springer
While 2/3 of patients with ATRT are less than 3 years at diagnosis, the literature suggests
younger children present with more aggressive disease and poorer outcome. However, little …