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 …

Atypical teratoid rhabdoid tumor: current therapy and future directions

KF Ginn, A Gajjar - Frontiers in oncology, 2012 - frontiersin.org
Atypical teratoid rhabdoid tumors (ATRTs) are rare central nervous system tumors that
comprise approximately 1–2% of all pediatric brain tumors; however, in patients less than 3 …

Relevance of molecular groups in children with newly diagnosed atypical teratoid rhabdoid tumor: results from prospective St. Jude multi-institutional trials

SA Upadhyaya, GW Robinson, A Onar-Thomas… - Clinical cancer …, 2021 - AACR
Purpose: Report relevance of molecular groups to clinicopathologic features, germline
SMARCB1/SMARCA4 alterations (GLA), and survival of children with atypical teratoid …

Inhibition of DNA damage repair by the CDK4/6 inhibitor palbociclib delays irradiated intracranial atypical teratoid rhabdoid tumor and glioblastoma xenograft …

R Hashizume, A Zhang, S Mueller, MD Prados… - Neuro …, 2016 - academic.oup.com
Background Radiation therapy is the most commonly used postsurgical treatment for primary
malignant brain tumors. Consequently, investigating the efficacy of chemotherapeutics …

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: improved long‐term survival with an intensive multimodal therapy and delayed radiotherapy. The Medical University of Vienna …

I Slavc, M Chocholous, U Leiss, C Haberler… - Cancer …, 2014 - Wiley Online Library
Atypical teratoid rhabdoid tumors (ATRT s) are recently defined highly aggressive
embryonal central nervous system tumors with a poor prognosis and no definitive guidelines …

Inhibition of EZH2 suppresses self-renewal and induces radiation sensitivity in atypical rhabdoid teratoid tumor cells

I Alimova, DK Birks, PS Harris, JA Knipstein… - Neuro …, 2013 - academic.oup.com
Abstract Introduction. Overexpression of the Polycomb repressive complex 2 (PRC2) subunit
Enhancer of Zeste 2 (EZH2) occurs in several malignancies, including prostate cancer …

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 …

CAR T cell therapy for pediatric brain tumors

JD Patterson, JC Henson, RO Breese… - Frontiers in …, 2020 - frontiersin.org
Chimeric Antigen Receptor (CAR) T cell therapy has recently begun to be used for solid
tumors such as glioblastoma multiforme. Many children with pediatric malignant brain …