President's Message
About CBTRUS
Acknowledgement
News and Events
Funding
Board of Directors
Board of Advisors
Personnel
Reports and Tables
Search Statistics
Manuscripts
Fact Sheet
Data Analysis Request
Links
Glossary
Contact Information
Home



RESULTS


Primary Brain Tumors: Incidence Rates by Gender, Race, and Age

The number of reported brain tumors from the participating registries is listed by state in Table 2. Over 42,500 tumors were reported to CBTRUS in a combined population of 61.5 million that represents approximately 23% of the U.S. population. The overall percent of benign tumors (38%) varied considerably by state (range: 23-55%). Eighty-two percent of all tumors had a histologically confirmed diagnosis, with substantial regional variation (state range: 73-99%).

The overall incidence rate for primary brain and central nervous system tumors was 12.7 per 100,000 person-years adjusted with the year 2000 standard (Table 3). The incidence rates by tumor behavior and state are shown in Figure 2. The total state incidence rates (adjusted using the Year 2000 standard) ranged from 9.6 to 19.5 per 100,000 person-years. The state rates for the malignant tumors are much less variable than the reported rates for the non-malignant tumors suggesting greater consistency in reporting of the malignant tumors. The state variation shown here, especially in reported incidence rates for the benign tumors, likely reflects differences in registry reporting practices including case ascertainment. A more detailed discussion of state reporting differences is available9.

The distribution of tumors by site is shown in Figure 3. The majority of tumors (61%) are located within the brain. Other CNS tumors, including meninges represent about 31% of all tumors reported to CBTRUS. The pituitary and pineal glands account for about 8% of tumors reported to CBTRUS.

The distribution by histology is shown in Table 4 and Figure 4. The most frequently reported histology is a predominately benign tumor meningioma, which account for over 25% of all tumors, followed closely by glioblastomas and astrocytomas. The predominately benign nerve sheath tumors and pituitary adenomas/carcinomas account for 7% and 6% of all tumors respectively.

The mean age of diagnosis for all primary brain tumors is 54 years (Table 4). The histology-specific mean ages range from 16 to 63 years. Pilocytic astrocytomas, medulloblastomas, and germ cell tumors have a mean age of onset under 20 years of age. Meningiomas and glioblastomas are diagnosed at older ages. The incidence rates by histology and gender are presented in Table 5. Rates for all primary brain tumors combined are higher among males than females. Rates for most histologies are higher in males or comparable to the rates in females with the notable exception of meningiomas that are twice as common in women. Incidence rates by histology and race are shown in Table 6. Overall rates are higher in Caucasians as compared to African-Americans. The age-specific rates by histology are presented in Table 7. The incidence for all brain tumors is highest among the 75-84 year olds. However, the different histologies have different age distributions as shown in this table. The histologic-specific differences in brain and CNS tumor distribution by age, gender, and race suggest that these tumors have different causes.

Brain tumors are the second most common malignancy among children10. About 8% of the tumors reported to CBTRUS occurred in people under the age of 20 years. The incidence of the most common childhood tumors is shown in Table 8 and the age-specific rates are shown in Table 9. Among the younger population brain tumors are slightly more common in boys. The most common histologies in the younger age group include embryonal tumors (medulloblastomas) and pilocytic astrocytomas that together account for over 30% of all childhood brain tumors. (Figure 5)

Malignant Brain Tumor Rates: Incidence, Mortality, and Survival

State incidence and mortality rates for primary malignant brain and CNS tumors are shown in Table 10. These rates are adjusted using the 1970 U.S. standard population. The 1993-1997 mortality rates by gender are available for all 50 states. Incidence rates for most states were available from the same time period with a few exceptions. These data were obtained from the most recent Cancer Incidence in North America publication available at http://www.naaccr.org6.

Survival estimates by tumor location, histology, and age at diagnosis are presented in Tables 11, 12, and 13 respectively. Survival is poorer for tumors located in the upper regions of the brain (Table 11). Patients with tumors in the meninges and the pituitary have better five-year survival rates. The two-, five-, and ten-year observed and relative survival rates by histology are shown in Table 12. There is a large variation in survival estimates between tumor histologies. Five-year survival rates exceed 85% for pilocytic astrocytomas but are less than 5% for glioblastomas. The estimated five- and ten-year relative survival rates for malignant brain tumors are 27% and 23% respectively. Survival generally decreases with older age at diagnosis (Table 13). Children and young adults have better survival for most histologies.

Histology-specific summary information

The information presented in these tables can be synthesized to describe specific histologies. As an example we have chosen the two most common histologies, meningiomas and glioblastomas. Meningiomas are the most frequently reported tumor and account for almost 26% of tumors reported to CBTRUS. Meningiomas are predominately a benign tumor type. Over 90% of meningiomas reported to CBTRUS had a benign behavior code. Glioblastomas (GBMs) are the second most frequently reported histology and the most common malignancy. They account for 23% of all primary brain tumors. (Table 3) Both of these histologies are more common in older adults (mean age at diagnosis is 62 years) (Table 3) and are uncommon in children. Glioblastomas comprise less than 5% of all tumors reported among 0-19 year olds (Table 8). The incidence of glioblastomas and meningiomas increases with increasing age. The rates for glioblastomas are highest in 65 to 84 years olds. The rates for meningiomas increase dramatically after age 65 and continue to be high even among the population aged 85 and older. (Table 7) Meningiomas are almost twice as common in females as compared to males while glioblastomas are 1.6 times more common in males. (Table 5) The incidence in meningiomas is similar between whites and African Americans while glioblastomas are over two times higher among whites as compared to blacks. (Table 6) The observed survival estimates for glioblastoma are quite low; less than 3% of patients survived 5 years post diagnosis. (Table 12) Glioblastoma survival estimates are somewhat higher for the small number of patients who are diagnosed under age 20 (Table 13). Only malignant meningiomas are reported in the SEER database and survival estimates were not generated. Further information about meningioma survival estimates was previously estimated using data reported to the National Cancer DataBase and is summarized elsewhere11.

SUMMARY


These data present an updated summary (1992-1997) of the incidence of all primary brain tumors and incidence, mortality and survival for all primary malignant brain tumors in the United States. We hope that these data are useful to clinicians, researchers, and patient families. CBTRUS encourages all cancer registries to include the collection of non-malignant primary brain tumors.

REFERENCES


1. Percy C, Van Holten V, and Muir CM (eds). (1996) International Classification of Diseases for Oncology, second edition, World Health Organization, Geneva, Switzerland.
2. U.S. populations. Bethesda, MD, National Cancer Institute. World Wide Web URL: http://www-seer.ims.nci.nih.gov
3. EDITS version 2.00 (Feb. 7, 1997) Division of Cancer Prevention and Control, National Center for Chronic Disease Prevention and Health Promotion. CDC, U.S Public Health Service, Department of Health and Human Services.
4. Kleihues P, Burger PC, and Scheithauer BW (1993) The new WHO classification of brain tumors. Brain Pathology, 3: 255-268.
5. SAS language and procedures: Usage, version 6, 1st edition (1989). SAS Institute, Cary, NC.
6. Cancer in North America (CINA), 1993-1997 Volume One (Incidence) and Volume Two (Mortality) 2000, http://www.naaccr.org
7. Ries LAG, Eisner MP, Kosary CL, Hankey BF, Miller BA, Clegg L, Edwards BK (eds). Surveillance, Epidemiology, and End Results (SEER) Cancer Statistics Review, 1973-1997, National Cancer Institute, Bethesda, MD, 2000.
8. Surveillance, Epidemiology, and End Results (SEER) Program Public-Use CD-ROM (1973-1996), National Cancer Institute, DCCPS, Cancer Surveillance Research Program, Cancer Statistics Branch, issued April 1999, based on the August 1998 submission.
9. Surawicz TS, McCarthy BJ, Jukich PJ, Davis FG. The accuracy and completeness of primary brain and central system tumor data: Results from the Central Brain Tumor Registry of the United States. Journal of Registry Management. 27(2):51-55, 2000.
10. Gurney JG, Smith MA, and Bunin GR. Chapter III CNS and miscellaneous intracranial and intraspinal neoplasms. In: Ries LAG, Smith MA, Gurney JG, Linet M, Tamra T, Young JL, Bunin GR (eds). Cancer Incidence and Survival among Children and Adolescents: United States SEER Program 1975-1995, National Cancer Institute, SEER Program. NIH Pub. No. 99-4649. Bethesda, MD, 1999. http://www-seer.ims.nci.nih.gov
11. McCarthy B, Davis F, Freels S, Surawicz T, Damek D, Grutsch J, Menck H, Laws E (1998) Factors associated with survival in patients with meningioma. Journal of Neurosurgery, 88:831-839.

Disclaimer

The Central Brain Tumor Registry of the United States (CBTRUS) is a not-for-profit corporation which gathers and disseminates epidemiologic data on primary brain tumors in order to facilitate research and establish awareness of the disease. CBTRUS makes no representations or warranties, and gives no other assurances or guarantees, express or implied, with respect to the accuracy or completeness of the data presented. The information provided in this website is not intended to assist in the evaluation, diagnosis or treatment of individual diseases. Persons with questions regarding individual diseases should contact their own physician to obtain medical assistance.