Defining future directions in spinal cord tumor research

Proceedings from the National Institutes of Health workshop

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The relative rarity of spinal cord tumors has hampered the study of these uncommon nervous system malignancies. Consequently, the understanding of the fundamental biology and optimal treatment of spinal cord tumors is limited, and these cancers continue to inflict considerable morbidity and mortality in children and adults. As a first step to improving the outcome of patients affected with spinal cord tumors, the National Institutes of Health Office of Rare Diseases Research in cooperation with the National Cancer Institute and the National Institute of Neurological Disorders and Stroke convened a workshop to discuss the current status of research and clinical management of these tumors. The overall goal of this meeting was to initiate a process that would eventually translate fundamental basic science research into improved clinical care for this group of patients. Investigational priorities for each of these areas were established, and the opportunities for future multidisciplinary research collaborations were identified.

Abbreviations used in this paper:CBTRUS = Central Brain Tumor Registry of the United States; NIH = National Institutes of Health.

Article Information

Address correspondence to: Elizabeth B. Claus, M.D., Ph.D., Department of Epidemiology and Public Health, Yale University School of Medicine, 60 College Street, P.O. Box 208034, New Haven, CT 06520-8034. email: elizabeth.claus@yale.edu or Richard J. Gilbertson, M.D., Ph.D., Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, Tennessee 38105-3678. email: Richard.Gilbertson@stjude.org.

© AANS, except where prohibited by US copyright law.

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