Journal article
Medulloblastoma Down under 2013: A report from the third annual meeting of the International Medulloblastoma Working Group
NG Gottardo, JR Hansford, JP McGlade, F Alvaro, DM Ashley, S Bailey, DL Baker, F Bourdeaut, YJ Cho, M Clay, SC Clifford, RJ Cohn, CH Cole, PB Dallas, P Downie, F Doz, DW Ellison, R Endersby, PG Fisher, T Hassall Show all
Acta Neuropathologica | SPRINGER | Published : 2014
Abstract
Medulloblastoma is curable in approximately 70 % of patients. Over the past decade, progress in improving survival using conventional therapies has stalled, resulting in reduced quality of life due to treatment-related side effects, which are a major concern in survivors. The vast amount of genomic and molecular data generated over the last 5-10 years encourages optimism that improved risk stratification and new molecular targets will improve outcomes. It is now clear that medulloblastoma is not a single-disease entity, but instead consists of at least four distinct molecular subgroups: WNT/Wingless, Sonic Hedgehog, Group 3, and Group 4. The Medulloblastoma Down Under 2013 meeting, which con..
View full abstractGrants
Awarded by Eunice Kennedy Shriver National Institute of Child Health and Human Development
Funding Acknowledgements
The Telethon Adventurers (http://www.theadventurers.com.au), a Western Australian charity dedicated to finding a cure for childhood brain cancer, provided financial support for the meeting. The participants thank Rick Parish and Peter Wilson, founders of the Telethon Adventurers, and all those whose fundraising efforts made this meeting possible. We also thank Angela McArthur for scientific editing of this report.