Literature DB >> 29016845

Pediatric low-grade gliomas: next biologically driven steps.

David T W Jones1, Mark W Kieran2, Eric Bouffet3, Sanda Alexandrescu4, Pratiti Bandopadhayay2, Miriam Bornhorst5,6, David Ellison7, Jason Fangusaro8, Michael J Fisher9, Nicholas Foreman10, Maryam Fouladi11, Darren Hargrave12, Cynthia Hawkins13, Nada Jabado14, Maura Massimino15, Sabine Mueller16, Giorgio Perilongo17, Antoinette Y N Schouten van Meeteren18, Uri Tabori3, Katherine Warren2,19, Angela J Waanders9, David Walker20, William Weiss16, Olaf Witt1, Karen Wright, Yuan Zhu5, Daniel C Bowers21, Stefan M Pfister1, Roger J Packer5,22.   

Abstract

Despite the fact that they are not typically life-threatening, low-grade gliomas (LGGs) remain a significant clinical challenge in pediatric neuro-oncology due to comorbidities associated with these tumors and/or their treatments, and their propensity to multiply recurs. LGGs, in total the most common brain tumors arising in childhood, can often become a chronic problem requiring decades of management. The Second International Consensus Conference on Pediatric Low-Grade Gliomas held in Padua, Italy in 2016 was convened in an attempt to advance the pace of translating biological discoveries on LGGs into meaningful clinical benefit. Topics discussed included: the implications of our growing biological understanding of the genomics underlying these tumors; the assessment of the model systems available; the implications of the molecular and histopathologic differences between adult and pediatric diffuse gliomas; and steps needed to expedite targeted therapy into late-stage clinical trials for newly diagnosed cases. Methods for the diagnostic assessment of alterations in the Ras/mitogen-activated protein kinase pathway, typical for these tumors, were also considered. While the overall tone was positive, with a consensus that progress is being and will continue to be made, the scale of the challenge presented by this complex group of tumors was also acknowledged. The conclusions and recommendations of the meeting panel are provided here as an outline of current thinking and a basis for further discussion.
© The Author(s) 2017. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  MAPK pathway; low-grade glioma; molecular diagnostics; neurooncology; pediatric brain tumor; targeted therapy

Mesh:

Year:  2018        PMID: 29016845      PMCID: PMC5786244          DOI: 10.1093/neuonc/nox141

Source DB:  PubMed          Journal:  Neuro Oncol        ISSN: 1522-8517            Impact factor:   12.300


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