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| Volume 3 Issue 61 | Editor: Susan K. Boyer, RN © RAmEx Ars Medica, Inc. All rights reserved. |
Questions And Answers:
Annual Report To The Nation On The Status Of Cancer, 1973-1998; Feature Focuses On Cancers With Recent Increasing Trends
1. What is the purpose of this report and who created it? This report provides an update on the trends in cancer incidence (new cases reported) and death rates in the United States. It also features a section on a dozen cancers with upward trends compared to the majority of cancers which are decreasing. The North American Association of Central Cancer Registries (NAACCR); the Centers for Disease Control and Prevention (CDC), including the National Center for Health Statistics (NCHS); the American Cancer Society (ACS); and the National Cancer Institute (NCI) collaborated to create this report. These reports are issued annually.
Information on newly diagnosed cancer cases occurring in the United States is based on data collected by registries in the NCI's Surveillance, Epidemiology, and End Results (SEER) Program and the CDC's National Program of Cancer Registries (NPCR), which are put together annually and published by the North American Association of Central Cancer Registries (NAACCR). The SEER Program, which began in 1973, collects cancer incidence data from geographic areas comprising 14 percent of the U.S. population. The NPCR, authorized in 1992, expands data collection and operations in existing cancer incidence registries and plans and implements new registries in states and U.S. territories where ones did not previously exist. NAACCR evaluates and publishes data annually from registries in both programs. Cancer mortality information in the United States is based on causes of death reported by physicians on death certificates. The mortality information is processed and consolidated into a national database by the NCHS through the National Vital Statistics System.
Cancer incidence rates increased from 1973 to 1982 and the increase accelerated from 1982 to 1992. Incidence rates for all cancer sites combined decreased on average 1.1 percent per year from 1992 to 1998. This confirms the continued downward trend that has been reported to the nation for the past four years. Cancer death rates increased from 1973 to 1991, were level from 1991
to 1994, and declined 1.4 percent per year from 1994 to 1998. In this report, cancer incidence and death rates are described for whites, blacks, Asian and Pacific Islanders, American Indians/Alaska Natives, and Hispanics. Hispanic is not mutually exclusive from whites, blacks, and Asian and Pacific Islanders. Supplemental information on the report can be found at http://seer.cancer.gov. Additional information on trends can be found on SEER's Cancer Statistics Review at http://seer.cancer.gov/Publications/CSR1973_1998/.
Continued higher incidence and death rates among some racial and ethnic groups suggest that not all populations have benefitted equally from cancer prevention and treatment control efforts. Such disparities may be due to multiple factors, such as late stage of disease at diagnosis, barriers to health care access, history of other diseases, biologic and genetic differences in tumors, health behaviors, and the presence of risk factors. The four leading cancer incidence sites for the five racial and ethnic populations were: lung and bronchus, prostate, female breast, and colorectum. Together these four sites account for over half of all new diagnoses. When these four cancer sites were examined by race and ethnicity, it was found that except for female breast cancer, blacks had higher incidence and death rates than the other racial and ethnic populations. Some cancer sites tended to be unique to a specific population. For example, melanoma and leukemia were among the top 10 sites only in whites; liver cancer was among the top 10 sites only in Asian and Pacific Islanders; kidney and renal pelvis cancers were among the top 10 only in American Indian/Alaska Natives; and bladder cancer was among the top 10 only in whites and Hispanics. The four leading cancer death sites from 1992 to 1998 for the racial and ethnic groups were the same sites as for incidence: lung and bronchus, prostate, female breast, and colorectum. When these four mortality sites were examined by race and ethnicity, blacks had higher cancer death rates than whites, Asian and Pacific Islanders, American Indians/Alaska Natives, or Hispanics. In April 2000, the NCI established Special Populations Networks, which will distribute a total of $60 million in grants over five years to address some of these disparities. In collaboration with other state and nonprofit organizations, CDC and NCI support various activities aimed toward reducing disparities in cancer, including the CDC's Initiative to Eliminate Racial and Ethnic Disparities and the National Institutes of Health Disparities Plan.
Lung cancer is the number one cause of cancer death among men and women in all racial and ethnic groups except for Hispanic women. Female lung cancer is one of the 12 cancers showing increasing trends. Due to a lag in smoking cessation trends, death rates for women have increased 0.8 percent per year between 1992 to 1998, although there has been a gradual slowing in female lung cancer death rates over the past three decades. Death rates for men decreased 1.9 percent per year from 1992 to 1998. Lung cancer mortality began to decrease in 1990 in men but the increase in mortality continued until at least 1998 in women.
7. What is happening with breast cancer rates in women? Female breast cancer represents one of the dozen cancers with an upward statistical trend, showing a 1.2 percent per year increase in incidence rates from 1992 to 1998. Long-term trends in invasive breast cancer incidence rates show an increase of more than 40 percent, from 82.6 per 100,000 to 118.1 per 100,000 from 1973 to 1998. Increases were limited to early stage (I and II) cancers. In addition, in situ cancer is also increasing in women over the age of 50. These trends may be related to increased screening during this period, particularly with mammograms. The extent to which other factors, such as increases in obesity and post-menopausal hormone use, may contribute to the increase is unknown. Breast cancer death rates decreased 1.6 percent annually from 1989 to
1995, then declined more rapidly to 3.4 percent per year between 1995
and 1998, probably due to improvements in early detection and treatment.
Breast cancer was the leading cause of cancer deaths in Hispanic women
and the death rate was highest among black women. 8. What is happening with prostate cancer rates? Prostate cancer incidence rates have fluctuated dramatically. Incidence
rates increased rapidly between 1988 and 1992 with the introduction of
Prostate Specific Antigen testing and then decreased after 1992. Prostate
cancer is the most commonly diagnosed cancer incidence site in men for
all racial and ethnic groups. Incidence rates varied from 101.0 per 100,000
for white men in Kentucky to 262.6 per 100,000 for black men in the Atlanta
metropolitan area. Prostate cancer death rates have also varied over time,
and death rates for blacks and whites have steadily declined since the
mid-1990s. Death rates in black men are double those of other racial and
ethnic groups. 9. What is happening with colorectum cancer rates? 10. What are the 10 other cancers that are showing upward trends? In addition to the recent rise in female breast cancer incidence rates and the long-term increase in female lung cancer death rates, an increase in either incidence or death rates between 1992 to 1998 has been observed for ten other cancer sites. Below is a list of those less common cancers, in descending order of their contribution to total cancer deaths:
A number of strategies were identified, with reduction in tobacco use
being the most significant since tobacco smoking causes an estimated 30
percent of all cancer deaths. Other prevention programs, such as sunscreen
education to reduce melanoma rates, immunization against hepatitis B to
prevent chronic hepatitis B virus (HBV) infection A second strategy identified was improved use of effective but underutilized screening techniques, such as colonoscopy for colorectal cancer and mammography for breast cancer. Coupled with this strategy is the need to develop more effective screening and detection tools. Thirdly, development of state-of-the-art diagnostic tests and treatments and the use of these tests to more accurately guide and direct treatment were suggested. This is particularly important in the drive to develop and use molecularly targeted drug regimens. The fourth strategy was identifying and reducing disparities across diverse populations by disseminating cancer treatment to all populations to increase survival, improve quality of life, and decrease mortality. Training programs to increase the diversity of scientists in biomedical research and to enhance existing careers were offered as viable strategies. Finally, support of a national cancer surveillance system that collects information across the entire life cycle was seen as important. Information could be used to target populations with prevention and early detection initiatives, to focus research, and to improve access to treatment and palliative care for all cancer patients and survivors.
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