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Neuro Oncol 1999 1(3):205-211; DOI:10.1215/15228517-1-3-205
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Symposia Epidemiology of Brain Tumors

Centralized databases available for describing primary brain tumor incidence, survival, and treatment: Central Brain Tumor Registry of the United States; Surveillance, Epidemiology, and End Results; and National Cancer Data Base

Faith G. Davis, Bridget J. McCarthy2 and Mitchel S. Berger

Department of Biostatistics/Epidemiology, University of Illinois at Chicago, Chicago, IL 60612 (F.G.D, B.J.M.); and Department of Neurosurgery, University of California at San Francisco, San Francisco, CA 94143 (M.S.B.)

2 Address correspondence and reprint requests to Bridget J. McCarthy, PhD, Department of Biostatistics/Epidemiology, University of Illinois at Chicago, 2121 W. Taylor, M/C 922, Chicago, IL 60612.

Abstract

Characteristics of three databases—the Central Brain Tumor Registry of the United States (CBTRUS) database; the Surveillance, Epidemiology and End Results (SEER) database; and the National Cancer Data Base (NCDB)— containing information on primary brain tumors are discussed. The recently developed population-based CBTRUS database comprises incidence data on all primary brain tumors from 11 collaborating state registries; however, follow-up data are not available. SEER, the population-based gold standard for cancer data, collects incidence and follow-up data on malignant brain tumors only. While not population-based, the NCDB identifies newly diagnosed cases and conducts follow-up on all primary brain tumors from hospitals accredited by the American College of Surgeons. The NCDB is the largest of the three databases and also contains more complete information regarding treatment of these tumors than either the SEER or CBTRUS databases. Additional strengths and limitations of each of these are described, and their judicious use for supporting research, education, and health care planning is encouraged.


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Copyright 1999 by Society for Neuro-Oncology