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Dr. Smith is Director of Cancer Screening, Cancer Control Science Department, American Cancer Society, Atlanta, GA.
Dr. Cokkinides is Program Director for Risk Factor Surveillance, Department of Epidemiology and Research Surveillance, American Cancer Society, Atlanta, GA.
Dr. Eyre is Executive Vice President for Research and Medical Affairs, American Cancer Society, Atlanta, GA, and Editor in Chief of CA.
| ABSTRACT |
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| INTRODUCTION |
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In 2001, the ACS published revisions in the early detection guidelines for colorectal, endometrial, and prostate cancers, and also an updated narrative related to testing for early lung cancer detection.2 Guidelines for cervical cancer screening were updated in 2002.5 In 2003, guidelines for the early detection of breast cancer and a modification of the recommendations for fecal occult blood testing for colorectal cancer screening were published.6,7
In addition to providing an overview of existing ACS recommendations for early cancer detection, in this issue we provide (1) a brief summary of updated ACS guidelines for breast cancer screening; (2) a brief update on guidelines and new technologies for colorectal cancer screening; (3) a summary of updated recommendations for cervical cancer screening issued by the US Preventive Services Task Force (USPSTF) and a comparison of USPSTF guidelines and ACS guidelines for cervical cancer screening; and (4) a summary of current screening rates among adults in the United States.
| SCREENING FOR BREAST CANCER |
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The ACS recommendations for clinical breast examination remain unchanged with respect to age-specific periodicity. Clinical breast examination should be performed every three years in women between the ages of 20 and 39 years, and annually for women aged 40 and older. This examination, which should occur during periodic health checkups, provides an opportunity to access risk, to discuss the importance of early detection, to discuss the importance of regular mammography in women aged 40 years and older, and to answer any questions patients may have about their own risk, new technologies, or other matters related to breast cancer. There may be some benefit to performing the clinical breast examination before the mammogram.6 Women who choose to do BSE can have their technique reviewed during these encounters.
Guidelines for mammography remain unchanged. Women at average risk should begin regular mammography at age 40 years. Women also should be informed about the benefits, limitations, and potential harms associated with screening. The importance of adherence to a schedule of annual mammograms should be stressed.
The update of the breast cancer screening guidelines also addressed issues related to screening high-risk groups, the age to stop screening, and screening with new technologies. Although there are not yet sufficient data to recommend a specific surveillance strategy for women at higher risk, the update states that women at increased risk for breast cancer may benefit from earlier initiation of screening, screening at shorter intervals, and screening with additional methods such as ultrasound or magnetic resonance imaging. With respect to the age to stop screening mammography, the ACS recommends that these decisions should be individualized by considering the potential benefits and risks of screening in the context of overall health status and longevity. The guidelines narrative stressed the tendency of clinicians to underestimate longevity in older women who would still likely benefit from preventive health strategies. As long as a woman is in good health and would be a candidate for treatment, she should continue to be screened with mammography.
| SCREENING FOR CERVICAL CANCER |
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The ACS recommends that cervical cancer screening should begin approximately three years after the onset of vaginal intercourse, but no later than age 21 years. Cervical screening should be performed annually until age 30 with conventional cervical cytology, or every two years until age 30 using liquid-based cytology, after which screening may continue every two to three years for those women who have had three consecutive, technically satisfactory normal/negative cytology results. Women aged 70 and older with an intact cervix may choose to cease cervical cancer screening if they have had three or more documented, consecutive, technically satisfactory normal/negative cervical cytologic test results and also no abnormal/positive cytologic test results within the 10-year period before age 70.
The update of the guidelines also addressed screening for cervical cancer in women for whom additional guidance is relevant. Women with a history of cervical cancer, in utero exposure to diethylstilbestrol, or who are immunocompromised (including those who test positive for the human immunodeficiency virus) should continue cervical cancer screening for as long as they are in reasonably good health.
Cervical cancer screening is not indicated for women who have had a total hysterectomy (with removal of the cervix) for benign gynecologic disease. However, women who have had a subtotal hysterectomy should be screened according to the recommendations for women at average risk. Women with a history of cervical intraepithelial neoplasia (CIN) 2/3 who have undergone hysterectomy, or for whom it is not possible to document the absence of CIN 2/3 as an indication for hysterectomy, should be screened until three documented, consecutive, technically satisfactory normal/negative cervical cytology results and no abnormal/positive cytology results (within a 10-year period) are achieved. Women with a history of in utero diethylstilbestrol exposure or a history of cervical carcinoma should continue screening after hysterectomy for as long as they are in reasonably good health and do not have a life-limiting chronic condition.
When the updated guidelines were published,5 the ACS addressed the use of human papilloma virus (HPV) DNA testing with cytology as a primary screening test for cervical cancer. There are several potential benefits of HPV DNA testing. Women who have negative results of both cervical cytology and HPV DNA tests are further reassured that they are at low risk for cervical cancer. Women who have repeated positive results for high-risk HPV subtypes are at higher risk for cervical cancer and may potentially benefit from more intensive surveillance. Although the Food and Drug Administration (FDA) had not yet approved HPV DNA testing with cytology as a screening test when the guidelines were published in 2002, the ACS recommended, pending FDA approval, that HPV DNA testing with cytology would be reasonable for screening women aged 30 years and older as an alternative to cytologic examination alone. Based on both published and unpublished data reviewed in the guidelines development process, the ACS recommended that cervical cancer screening with HPV DNA testing and conventional or liquid-based cytology could be performed every three years. The ACS guidelines update also stressed the need to develop management algorithms for women with normal/negative cytology results but positive test results for high-risk HPV DNA subtypes.
The ACS discouraged HPV testing any more frequently than every three years and stressed that women who choose to undergo HPV DNA testing should receive counseling and education about HPV. For instance, a positive HPV test result should not be viewed as indicating the presence of a sexually transmitted disease, but rather a sexually acquired infection. Nearly every person who has had sexual intercourse has been exposed to HPV, and the infection is extremely common and usually not detectable or harmful. Testing positive for HPV does not indicate the presence of cancer, nor will the large majority of infections foretell an eventual cancer.
In March 2003, the FDA approved expanded use of Digene Corporations Hybrid Capture 2 (HC2) HPV DNA test, which can screen for 13 high-risk strains of HPV associated with cervical cancer.
In January 2003, the USPSTF also updated guidelines for cervical cancer screening, with recommendations for average-risk women, women over age 65, and use of new technologies similar to the ACS update.10 The USPSTF found good evidence that screening with cervical cytology reduces incidence and mortality from cervical cancer, and indirect evidence indicating that most of the benefit can be obtained by beginning screening within three years of onset of sexual activity or age 21 (whichever comes first) and screening at least every three years. The USPSTF recommended against continuing cytologic screening for women aged 65 and older who have had adequate recent screening with normal results, and cited ACS criteria for continuing screening in instances where this criteria could not be met.
| SCREENING AND SURVEILLANCE FOR THE EARLY DETECTION OF ADENOMATOUS POLYPS AND COLORECTAL CANCER |
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The ACS recommends more intensive surveillance for (1) persons at increased risk due to a history of adenomatous polyps; (2) persons with a history of curative-intent resection of colorectal cancer; (3) persons with a family history of either colorectal cancer or colorectal adenomas diagnosed in a first-degree relative before age 60 years; (4) persons at significantly higher risk due to a history of inflammatory bowel disease of significant duration; or (5) persons at significantly higher risk due to a family history of or genetic testing indicating the presence of one of two hereditary syndromes.
In 2003, a consortium of gastroenterology societies also updated clinical guidelines for colorectal cancer screening and surveillance.12 The guideline stresses that persons at average risk who are 50 years and older should be screened for colorectal cancer using one of the acceptable options listed previously.
| SCREENING FOR ENDOMETRIAL CANCER |
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| SCREENING FOR PROSTATE CANCER |
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Men at high risk, including those of African descent (specifically sub-Saharan African descent) and those with a first-degree relative with the disease diagnosed at a younger age (ie, younger than 65 years) should begin testing at age 45. Men at even greater risk for prostate cancer because they have more than one first-degree relative with prostate cancer diagnosed before age 65 could begin testing at age 40. However, if the PSA level is less than 1 ng/mL, no additional testing is needed until age 45. If the PSA is greater than 1 ng/mL but less than 2.5 ng/mL, annual testing is recommended. If the PSA is 2.5 ng/mL or greater, further evaluation with biopsy should be considered. Men at high risk also should be informed about the benefits and limitations of testing for early prostate cancer detection and treatment of early prostate cancer.
| TESTING FOR EARLY LUNG CANCER DETECTION |
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The ACS historically has maintained that persons at high risk for lung cancer due to significant exposure to tobacco smoke or occupational exposures and their physicians may choose to have these screening tests done on an individual basis.13 The challenge associated with these personal decisions is more complicated today because of favorable findings from investigations using low-dose spiral CT to test for early lung cancer14,15 and aggressive promotion of these tests to persons at risk. Although these case series reports have demonstrated impressive performance of imaging with spiral CT and positron emission tomography, most organizations that issue screening guidelines likely will require more conventionally definitive results from the ongoing National Cancer Institute and American College of Radiology Imaging Networks collaborative National Lung Screening Trial before issuing guidelines for lung cancer screening.16 However, because these tests are being aggressively marketed to individuals, the ACS revised the narrative related to lung cancer screening to emphasize the importance of informed decision making for persons who choose to be tested for early lung cancer detection and to recommend that, ideally, testing should be done only in experienced centers that also are linked to multidisciplinary specialty groups for diagnosis and follow-up. Current smokers should be informed that the more immediate preventive health priority is the elimination of tobacco use altogether, because smoking cessation offers the surest route at this time to reducing the risk for premature death from lung cancer.17
| THE CANCER-RELATED CHECKUP |
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The ACS now recommends that the cancer-related checkup occur during a general periodic health examination, rather than as a stand-alone examination done at a specific interval based on a persons age (Table 1).
| SURVEILLANCE OF CANCER SCREENING: COLORECTAL, BREAST, CERVICAL, AND PROSTATE CANCERS |
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These data are from the Centers for Disease Control and Preventions (CDC) Behavioral Risk Factor Surveillance System (BRFSS) for 2002. They represent the most current data for estimating the prevalence of cancer screening in the United States. From its inception, the focus of the BRFSS has been to establish a surveillance system to collect data regarding population-based sociodemographics, health behaviors, and related health care factors known to affect chronic diseases and the health status of the general population.18 The BRFSS provides state-specific estimates for behavioral risk factors from ongoing statewide telephone surveys of civilian, noninstitutionalized adults aged 18 years or older living in households with a telephone.
The BRFSS is conducted annually in all 50 states, the District of Columbia, and Puerto Rico by state health departments in collaboration with the CDC. The BRFSS survey method includes standardized core questionnaires, complex multistage cluster sampling designs, and random-digit dialing methods to select households with telephones. Data are weighted to provide prevalence estimates representative of the states adult population. Weighted estimates (prevalence) and the standard error of the estimates were computed for the US population based on the combined state-level weighted data from states participating in the BRFSS in 2002.
Cervical Cancer Screening
In 2002, 86.2% of women aged 18 and older reported having a Pap test in the preceding three years. The high rate of participation in cervical cancer screening reflects a high acceptance of the Pap test among women and their providers as well as the convenience of testing during routine encounters with health care providers. Women who were 18 to 44 years old were more likely to have had a Pap test in the preceding three years compared with women aged 45 and older (88.1% versus 83.4%). In contrast, the prevalence of recent cervical cancer screening is 15% lower among women 65 and older compared with those aged 18 to 44 years (Table 2).
Breast Cancer Screening
In 2002, 61.5% of women aged 40 and older reported having a mammogram in the last year. The proportion of women who reported having a mammogram in the last year was 60.5% among those aged 40 to 64 years and 63.8% among those 65 and older. When considering breast cancer screening with both mammography and clinical breast examination, the estimates are lower, just slightly more than 50%. The proportion of women, aged 40 to 64 years, who reported having both a mammogram and a clinical breast examination in the previous year was 54.9%, and the proportion was 52.3% among women ages 65 and older (Table 2).
Prostate Cancer Screening
In 2002, the proportion of men aged 50 and older who reported having a PSA test in the previous year was 53.7%. The proportion of men reporting digital rectal examination in the previous year was 52% (Table 2).
Colorectal Cancer Screening
The proportion of adults aged 50 and older reporting recent colorectal cancer screening with an endoscopic procedure (either a sigmoidoscopy or colonoscopy) was nearly twice that of adults reporting recent screening with an FOBT. In 2002, 40.4% of adults in this age group reported having received either a sigmoidoscopy or colonoscopy procedure within the past five years, whereas the prevalence of having an FOBT within the past year was 21.8%. However, because the nationwide prevalence of colorectal cancer screening is only approximately 50% (ie, 53.1% of adults aged 50 years and older had an FOBT or lower endoscopy, or both), the substantial problem of too many average risk adults not being screened with any of the recommended tests persists.
It is important to note that this comparison represents an estimate of the prevalence of adults who are current with ACS guidelines in terms of the kind of testing they have undergone. However, because the BRFSS does not distinguish between sigmoidoscopy and colonoscopy, persons who had colonoscopy more than five years but less than 10 years before the survey was conducted would not be included in the estimate.2 No data are available from the BRFSS to estimate use of the double-contrast barium enema. There were no differences in the sex-specific prevalence of colorectal cancer screening (Table 2).
| STATE-SPECIFIC PREVALENCE IN THE LACK OF UTILIZATION OF BREAST AND COLORECTAL CANCER SCREENING |
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State-Specific Prevalence in the Lack of Breast Cancer Screening
Timely mammographic screening among women aged 40 years and older could prevent 30% to 48% of all deaths from breast cancer.6,19,20 In 2002, approximately 40% of American women aged 40 years and older reported that they had not had a mammogram within the last year. Despite the fact that mammography has been widely available since the late 1980s, in some states the prevalence of lack of mammographic screening among age-eligible women is notable. The state-specific prevalence in the lack of mammographic screening among age-eligible women was greater than 45% in nine states: Alaska, Arkansas, Idaho, Mississippi, New Mexico, Oklahoma, Texas, Utah, and Wyoming, with rates ranging from 45.1% to 48.9% (Figure 1).
State-Specific Prevalence in the Lack of Colorectal Cancer Screening
Colorectal cancer screening could reduce the colorectal cancer mortality rate by 50% or more through early detection of invasive disease and detection and removal of adenomatous polyps.21 In 2002, 50% of American men and women aged 50 years and older reported that they had not had any colorectal cancer screening (an FOBT within the last year or sigmoidoscopic screening). The state-specific prevalence of not having had any colorectal cancer screening tests (either an FOBT or a sigmoidoscopic examination according to screening guideline intervals) was more than 55% in South Dakota, Utah, Idaho, Hawaii, Louisiana, Mississippi, Nevada, Indiana, New Mexico, West Virginia, Arkansas, Oklahoma, and Wyoming, with rates ranging from 55.6% to 64.3% (Figure 2).
A recent report from the CDC showed slight improvements in the utilization of colorectal cancer screening procedures among persons at average risk between 1997 and 2001: 21% increase in FOBT use within the past year and 29% increase in lower endoscopy within the past five years.22 Compared with the use of other cancer screening tests, low colorectal cancer screening rates are a function of incomplete diffusion of proven and efficacious methods for screening in the health care systems, low engagement by health care providers in recommending screening to their patients, and lower awareness in the population about the need for and importance of screening.23–25
| CONCLUSIONS |
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A 2003 report from the Institute of Medicine highlighted the need for new strategies to prevent cancer and, when cancer occurs, to detect and treat it at its earliest stages.27 This report notes that the principal challenges to optimizing the delivery of effective cancer screening services, and reducing inappropriate testing, lie in changing the behaviors of three sectors of society: (1) systems of care, which should make cancer screening available to eligible populations; (2) health care providers, who should counsel patients about recommended cancer screening and assure that screening is performed in a timely manner; and (3) individuals, who should heed the recommendations made by public health agencies and their physicians on screening and obtain recommended screening tests and pursue follow-up tests. Among the recommendations for the nation to make progress in cancer prevention and early detection were specific recommendations related to early cancer detection. That is, there should be: (1) access to and coverage for early detection services by public and private insurers; (2) support for programs that provide primary care to the uninsured and underserved; (3) support for the CDCs National Breast and Cervical Cancer Early Detection Program; (4) the design and implementation of programs to improve health care provider education and training and adherence to evidence-based guidelines for early detection services; and (5) promotion of partnerships between public and private organizations to work toward improving the publics understanding of cancer prevention and early detection with a focus on prevention and early detection of cancer and reduction of disparities in the cancer burden. If key organizations would act on these recommendations with a vision toward improving adherence and efficiency in cancer screening and reducing disparities, then we could anticipate greater reductions in disease burden than we are achieving today.
| Footnotes |
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| REFERENCES |
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