SCREENING FOR COLORECTAL CANCER

Guidelines

1.       American Gastroenterological Association (AGA). Colorectal cancer screening: clinical guidelines and rationale. Gastroenterology 1997 Oct;113(4):1423-4 [220 references].

2.       U.S. Preventive Services Task Force (USPSTF). Screening for colorectal cancer. In: Guide to clinical preventive services. 2nd ed. Baltimore (MD): Williams & Wilkins, 1996. p. 89-103 [113 references].

3.       American Cancer Society (ACS). American Cancer Society guidelines on screening and surveillance for the early detection of adenomatous polyps and cancer-update 2001. In: American Cancer Society guidelines for the early detection of cancer. CA Cancer J Clin 2001 Jan-Feb;51(1):44-54 [181 references].

4.       Institute for Clinical Systems Improvement (ICSI). Colorectal cancer screening. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2000 Jan. 24 p. [49 references].

5.       Canadian Task Force on Preventive Health Care (CTFPHC). Preventive Health Care, 2001 Update: colorectal Cancer Screening. CMAJ 2001; 165(1):206-7 [97 references].

INTRODUCTION:

A direct comparison of AGA, USPSTF, ACS, ICSI, and CTFPHC recommendations for screening asymptomatic individuals and individuals at increased risk for colorectal cancer is provided in the following tables. In formulating their recommendations, ACS and CTFPHC review the conclusions drawn by AGA and USPSTF. ICSI considers the guideline released by USPSTF. Following the content comparison, areas of agreement and differences among the guidelines are discussed. In general, the timing of the guideline with respect to available data is an important factor to consider when evaluating areas of differences among guidelines. The rationale behind differences in practice recommendations that cannot be attributed to differences in the evidence base is also discussed.

The evidence supporting the major recommendations is also identified, with the definitions of the rating schemes used by USPSTF, ICSI and CTFPHC included in the last row of the table.

Abbreviations used in the text and tables follow:

·         ACS, American Cancer Society

·         AGA, American Gastroenterological Association

·         CRC, colorectal cancer

·         CTFPHC, Canadian Task Force on Preventive Health Care

·         DCBE, double contrast barium enema

·         DRE, digital rectal examination

·         FOBT, fecal occult blood testing

·         HNPCC, hereditary nonpolyposis colorectal cancer

·         ICSI, Institute for Clinical Systems Improvement

·         TCE, total colon examination

·         USPSTF, United States Preventive Services Task Force

 

OBJECTIVE AND SCOPE

AGA
(October, 1997)

  • To develop practical screening and surveillance guidelines for colorectal cancer (CRC) in average- and high-risk populations

USPSTF
(1996)

  • To present screening guidelines for colorectal cancer in adults at average and increased risk

ACS
(2001)

  • To address growing evidence concerning the benefits of early detection of colorectal cancer and adenomatous polyps

ICSI
(2000)

  • To reduce variation in screening for colorectal cancer (CRC)
  • To eliminate wasteful, unproductive processes for CRC screening
  • To increase patient participation in screening for CRC

CTFPHC
(2001)

  • To make recommendations on the effectiveness of specific screening techniques for colorectal cancer in asymptomatic patients

 

INTENDED USERS

AGA
(October, 1997)

Primary care clinicians and specialists

USPSTF
(1996)

Primary care clinicians

ACS
(2001)

Primary care clinicians and specialists

ICSI
(2000)

Primary care clinicians

CTFPHC
(2001)

Primary care clinicians and specialists

 

INTERVENTIONS AND PRACTICES CONSIDERED

AGA
(October, 1997)

Screening options:

  1. Fecal occult blood testing (FOBT), flexible sigmoidoscopy, or both
  2. Digital rectal examination (DRE) [Not recommended as the sole screening test but as a part of a screening examination]
  3. Double contrast barium enema (DCBE)
  4. Colonoscopy

Recommendations for high risk populations (i.e., counseling for genetic testing)

USPSTF
(1996)

Screening options:

  1. Fecal occult blood testing (FOBT), or sigmoidoscopy, or both
  2. Digital rectal examination (DRE) [Not recommended as the sole screening test]
  3. Double contrast barium enema (DCBE)
  4. Colonoscopy

High-risk patients are outside the scope of this guideline

ACS
(2001)

Screening options:

  1. Fecal occult blood testing (FOBT) or flexible sigmoidoscopy, or both
  2. Digital rectal examination (DRE) [Not recommended as the sole screening test but prior to sigmoidoscopy or colonoscopy]
  3. Double contrast barium enema (DCBE)
  4. Colonoscopy

Recommendations for high risk populations (i.e., counseling for genetic testing)

ICSI
(2000)

Screening options:

  1. Fecal occult blood testing (FOBT), flexible sigmoidoscopy, or both
  2. Digital rectal examination (DRE) [Not recommended as the sole screening test but as a part of a health evaluation]
  3. Double contrast barium enema (DCBE)
  4. Colonoscopy

High-risk patients are outside the scope of this guideline

CTFPHC
(2001)

Screening options:

  1. Fecal occult blood testing (FOBT), flexible sigmoidoscopy, or both as a part of multiphase screening
  2. Colonoscopy as a part of uniphase screening
  3. Genetic testing

Screening with digital rectal examination and double contrast barium enema were not considered because of the lack of direct evidence

COMPARISON OF RECOMMENDATIONS FOR SCREENING FOR COLORECTAL CANCER:
ADULTS, > 50 YEARS, NO OTHER RISK FACTORS

 

Fecal occult blood testing (FOBT)

AGA
(October, 1997)

  • An acceptable screening option is to offer FOBT on annual basis. This option is supported by strong evidence of effectiveness.

USPSTF
(1996)

  • Screening is recommended, based on fair evidence. Both FOBT and sigmoidoscopy are effective screening methods. There is insufficient evidence to determine which method is preferable.
  • There is good evidence to support FOBT on an annual basis.(B, II-1, II-2)

ACS
(2001)

  • FOBT annually is an acceptable screening option.
  • The take-home multiple sample method should be used.

ICSI
(2000)

  • An acceptable screening option is FOBT annually. (Evidence supporting the screening recommendations is of classes: C, R, B, D)

CTFPHC
(2001)

  • There is good evidence to include screening with Hemoccult test in the periodic health examination of asymptomatic patients over age 50 with no other risk factors [A, I].

    However, there remain concerns about the high rate of false-positive results, feasibility and small clinical benefit of such screening (over 1000 individuals must be screened for 10 years to avert one death from colorectal cancer). For patients being screened with Hemoccult, it is recommended that they avoid red meat, cantaloupe and melons, raw turnip, radishes, broccoli and cauliflower, vitamin C supplements and aspirin and non-steroidal anti-inflammatory drugs for 3 days before fecal samples are collected. However, a recent meta-analysis of 4 randomized controlled trials found no improvement in positivity rates or change in compliance rates with moderate dietary restrictions.

 

Flexible sigmoidoscopy

AGA
(October, 1997)

An acceptable screening option is to offer sigmoidoscopy every five years.

This option is supported by strong evidence of effectiveness. A five year interval is chosen because of strong (randomized trial) evidence that colonoscopy is equally effective at 1- or 1- and 3- year intervals, weaker (case control) evidence that sigmoidoscopy is effective at up to 10-year intervals, and the observation that few polyps arise and progress to advanced cancer in a 5 year period.

USPSTF
(1996)

Sigmoidoscopy is considered an effective screening technique; however, there is insufficient evidence to recommend a periodicity for sigmoidoscopy screening. (I-2, II-3)

ACS
(2001)

Flexible sigmoidoscopy performed every 5 years is an acceptable screening option.

This recommendation is supported by case-control studies of clinical effectiveness. The five year interval is chosen because of a range of factors that may affect the overall sensitivity of flexible sigmoidoscopy:

  • Flexible sigmoidoscopy is generally not done by specialists and thus the range of practitioner experience and expertise is variable.
  • Bowel preparation usually is less complete than for colonoscopy, meaning that important lesions may be obscured by stool.
  • Because no sedation is given with flexible sigmoidoscopy, patient discomfort or spasm may interfere with the completeness of the test.

ICSI
(2000)

An acceptable screening option is 60 cm flexible sigmoidoscopy every 5 years. (Evidence supporting the screening recommendations is of classes: C, R, B, D)

CTFPHC
(2001)

There is evidence from case control studies, to recommend that flexible sigmoidoscopy be included in the periodic health examination of patients over age 50 [B, II-2, III].

 

Combined fecal occult blood testing and flexible sigmoidoscopy

AGA
(October, 1997)

The individual components of this strategy are supported by strong evidence but the added value of combining the two, while theoretically present, is not well established by research evidence. Indirect evidence, including the panel’s decision analysis on the clinical consequences of CRC, supports this recommendation.

USPSTF
(1996)

There is insufficient evidence to determine whether this combination of tests produces greater benefits than either test alone.

ACS
(2001)

FOBT every year plus flexible sigmoidoscopy every 5 years is an acceptable screening option.

Because combining flexible sigmoidoscopy with FOBT can increase the benefits of either test alone, the ACS regards annual FOBT accompanied by flexible sigmoidoscopy every five years as a better choice than either FOBT or flexible sigmoidoscopy alone.

ICSI
(2000)

An acceptable screening option is a combination of both 60 cm flex sigmoidoscopy every 5 years and FOBT annually. (Evidence supporting the screening recommendations is of classes: C, R, B, D)

CTFPHC
(2001)

There is insufficient evidence to make recommendations about whether only 1 or both of FOBT and sigmoidoscopy should be performed [C, I].

 

Digital rectal examination (DRE)

AGA
(October, 1997)

DRE by itself has not been shown to be an effective way of screening for CRC.

However, it is part of other screening examinations for CRC (sigmoidoscopy, colonoscopy, and barium enema) and may be included in a comprehensive program of preventive health care for other reasons.

USPSTF
(1996)

DRE is of limited value as a screening test for CRC. There is insufficient evidence to recommend for or against routine screening with DRE.

Recommendations against using this test may be made on other grounds (e.g., availability of alternate tests of proven effectiveness, inaccuracy of DRE). (C, III)

ACS
(2001)

Although DRE is a useful method for identifying masses in the anal canal or lower rectum, it has very poor sensitivity for detecting colorectal cancer due to limited reach. While DRE is often included as part of a routine physical examination, it is not recommended as a stand-alone screening test for colorectal cancer. However, DRE should be performed prior to insertion of a sigmoidoscope or colonoscope.

ICSI
(2000)

DRE is a simple examination to perform with potential to discover a small percentage of colon cancers within reach of the examining finger. Palpation of any mass or polyp should lead to further investigation.

Separate health care encounters for the sole purpose of doing a DRE are not suggested. A DRE might be performed as part of a visit for either health evaluation or illness-related concerns.

CTFPHC
(2001)

Screening with digital rectal examination was not considered because of the lack of direct evidence.

 

Barium enema

AGA
(October, 1997)

An acceptable screening option is double contrast barium enema (DCBE) every 5-10 years.

This option is not supported by direct evidence (from randomized trial, nonrandomized trial, or case-control studies) that DCBE reduces mortality from CRC; but it is supported by the panel’s decision analysis on the clinical consequence of CRC.

USPSTF
(1996)

There is insufficient evidence to recommend for or against routine screening with barium enema.

Recommendations against using this test for screening average-risk persons may be made on other grounds (e.g., availability of alternate tests of proven effectiveness). (C, III)

ACS
(2001)

Examining the entire colorectum, either by colonoscopy every 10 years or by DCBE every 5 years is an acceptable screening option.

The choice of colonoscopy or DCBE for screening can be made on an individual basis, depending on factors such as personal preference, cost, feasibility, tolerance of potential complications, and the local availability of trained clinicians able to offer a high-quality examination. For those who elect either colonoscopy or DCBE for screening, there is no need for annual FOBT.

ICSI
(2000)

Acceptable screening option: perform total colon examination by flexible sigmoidoscopy combined with fluoroscopic barium enema or DCBE every 5 years. (Evidence supporting the screening recommendations is of classes: C, R, B, D)

CTFPHC
(2001)

Screening with double contrast barium enema was not considered because of the lack of direct evidence.

 

Colonoscopy

AGA
(October, 1997)

An acceptable screening option is colonoscopy every 10 years.

This option is not supported by direct evidence (from randomized trial, nonrandomized trial, or case-control studies) that colonoscopy reduces mortality from CRC; but it is supported by other evidence and the panel’s decision analysis on the clinical consequence of CRC.

USPSTF
(1996)

There is insufficient evidence to recommend for or against routine screening with colonoscopy.

Recommendations against using this test for screening average-risk persons may be made on other grounds (e.g., availability of alternate tests of proven effectiveness, costs and risks of colonoscopy). (C, III)

ACS
(2001)

Examining the entire colorectum, either by colonoscopy every 10 years or by DCBE every five years is an acceptable screening option.

The choice of colonoscopy or DCBE for screening can be made on an individual basis, depending on factors such as personal preference, cost, feasibility, tolerance of potential complications, and the local availability of trained clinicians able to offer a high-quality examination. For those who elect either colonoscopy or DCBE for screening, there is no need for annual FOBT.

ICSI
(2000)

An acceptable screening option is total colon examination, by colonoscopy every 5-10 years (Evidence supporting the screening recommendations is of classes: C, R, B, D)

CTFPHC
(2001)

There is insufficient evidence to include or exclude colonoscopy as an initial screen in the periodic health examination [C, II-3].

Although colonoscopy is the best method for detecting adenomas and carcinomas, it may not be feasible to screen asymptomatic patients because of patient compliance and the expertise and equipment required and the potential costs. On the other hand, if colonoscopy were an effective screening strategy when performed at less frequent intervals, these issues might be of less concern.

COMPARISON OF RECOMMENDATIONS FOR SCREENING FOR COLORECTAL CANCER:
PEOPLE AT INCREASED RISK FOR COLORECTAL CANCER

 

People with family history of colorectal cancer

AGA
(October, 1997)

People with a close relative (sibling, parent or child) who has had colorectal cancer or an adenomatous polyp should be offered the same options as average-risk people but beginning at age 40 years.

If the close relative was diagnosed with colorectal cancer before the age of 55 years or with an adenomatous polyp before age 60, special efforts should be made to assure that screening takes place.

USPSTF
(1996)

The increased risk of developing cancer at younger ages may justify beginning screening before age 50 (no specific age stated) in persons with a single first-degree relative with colon cancer, especially when affected relative developed CRC at younger ages.

ACS
(2001)

People with a family history of either colorectal cancer or colorectal adenomas that occurred in a first-degree relative before age 60, or in multiple first-degree relatives of any age (if not a hereditary syndrome), should have a colonoscopy* at age 40, or 10 years before the youngest case in the immediate family. Examination should be repeated every 5-10 years. Colorectal cancer in relatives more distant than first-degree does not increase risk substantially above the average risk group.

*Note: If a colonoscopy is not available, not feasible, or not desired by the patient, a DCBE, or flexible sigmoidoscopy followed by a DCBE can be used.

ICSI
(2000)

Patients at increased risk of developing colorectal cancer require colonoscopic surveillance at a 3 to 5 year interval, and are outside the scope of this guideline.

CTFPHC
(2001)

Patients who have only one or two first-degree relatives with colorectal cancer should be screened in the same way as average risk individuals. There is insufficient evidence to recommend colonoscopy for individuals who have a family history of colorectal polyps or cancer but do not fit the criteria for hereditary non-polyposis colon cancer [C, III]. While there is evidence that there is an increased prevalence of neoplasms in these individuals, there is insufficient information to recommend more intense screening than that of individuals at average risk. Further delineation of the risk for individuals with multiple affected family members and family members with early age of diagnosis of colorectal cancer is necessary.

 

People with a family history of familial adenomatous polyposis

AGA
(October, 1997)

Genetic counseling and consider genetic testing to see if they are gene carriers. Gene carriers or indeterminate cases should be offered flexible sigmoidoscopy every 12 months beginning at puberty to see if they are expressing the gene. If polyposis is present, they should begin to consider when they should have colectomy.

USPSTF
(1996)

Refer to specialist for regular endoscopic screening, diagnosis and management.

ACS
(2001)

Individuals with a family history of familial adenomatous polyposis are at high risk and should undergo early surveillance with endoscopy, and counseling to consider genetic testing beginning at puberty. If the genetic test is positive, colectomy is indicated; These patients are best referred to a center with experience in the management of familial adenomatous polyposis.

ICSI
(2000)

Patients at increased risk of developing colorectal cancer require colonoscopic surveillance at a 3 to 5 year interval, and are outside the scope of this guideline.

CTFPHC
(2001)

The Task Force recommends genetic testing of individuals at risk for familial adenomatous polyposis if the genetic mutation has been identified in the family and if genetic testing is available [B, II-3]. If the individual carries the mutation, then he or she should be screened with flexible sigmoidoscopy beginning at puberty [B, II-3]. Individuals from families where the gene mutation has been identified but are negative themselves, require screening similar to the average risk population. For at risk individuals where the mutation has not been identified in the family or where genetic testing is not available, screening with annual or biannual flexible sigmoidoscopy should be undertaken beginning at puberty. In all instances, genetic counseling should be performed prior to genetic testing.

 

People with a family history of hereditary nonpolyposis colorectal cancer (HNPCC)

AGA
(October, 1997)

Genetic counseling and consider genetic testing for HNPCC. Offer an examination of the entire colon every 1-2 years starting between the ages of 20 and 30 years and every year after age 40 years.

USPSTF
(1996)

Refer to specialist for regular endoscopic screening, diagnosis and management.

ACS
(2001)

Individuals with a family history of HNPCC should undergo colonoscopy and counseling to consider genetic testing beginning at age 21. If the genetic test is positive or if patient has not had genetic testing, colonoscopy is recommended every 1-2 years until age 40 years, then annually. These patients are best referred to a center with experience in the management of HNPCC.

ICSI
(2000)

Patients at increased risk of developing colorectal cancer require colonoscopic surveillance at a 3 to 5 year interval, and are outside the scope of this guideline.

CTFPHC
(2001)

Patients in kindreds with the cancer family syndrome (HNPCC) have a high risk of colorectal cancer and a high incidence of right-sided colon cancer. Thus, colonoscopy rather than sigmoidoscopy is recommended for screening such patients. Based on Level III evidence, the Task Force recommends screening with colonoscopy in individuals from hereditary non-polyposis colon cancer kindreds [B, II-3]. Although higher levels of evidence are usually required to give a B recommendation, the Task Force realizes that it is unlikely that more rigorous studies could be performed in this cohort of patients given the high risk of cancer and relative infrequency of hereditary non-polyposis colon cancer. The ages when screening should begin and the frequency at which colonoscopy should be performed are unclear.

 

People with a history of adenomatous polyps

AGA
(October, 1997)

Patients in whom large (>1-cm diameter) or multiple adenomatous polyps are found and removed at colonoscopy should have an examination of the colon 3 years after the initial examination. The interval for subsequent examinations depends on the type of polyps that were detected. If the first follow-up is normal or only a single, small, tubular adenoma is found, the next examination can be in 5 years. In special circumstances (e.g., polyps with invasive cancer, large sessile adenomas, or numerous adenomas), a shorter interval may be necessary, according to the judgment of the clinician and the wishes of the patient.

USPSTF
(1996)

Refer to specialist for regular endoscopic screening, diagnosis and management.

ACS
(2001)

People who have been diagnosed as having adenomatous polyps should have a colonoscopy to remove all polyps from the colorectum, after which a colonoscopic exam should be repeated at an interval to be determined on the basis of the size, multiplicity, and histologic appearance of the adenoma(s).

  • People with single, small (<1 cm) adenoma should be screened with colonoscopy* 3-6 years after the initial polypectomy. If the exam is normal, the patient can thereafter be screened as per average risk guidelines (see above).
  • People with a large (1 cm +) adenoma, multiple adenomas, or adenomas with high-grade dysplasia or villous change should be screened with colonoscopy* within 3 years after the initial polypectomy. If normal, repeat examination in 3 years; If normal then, the patient can thereafter be screened as per average risk guidelines (see above).

*Note: If a colonoscopy is not available, not feasible, or not desired by the patient, a DCBE, or flexible sigmoidoscopy followed by a DCBE can be used.

ICSI
(2000)

Patients at increased risk of developing colorectal cancer require colonoscopic surveillance at a 3 to 5 year interval, and are outside the scope of this guideline.

CTFPHC
(2001)

People with a history of adenomatous polyps are beyond the scope of the guideline.

 

People with a history of colorectal cancer

AGA
(October, 1997)

Patients with a colorectal cancer that has been resected with curative intent (but who did not undergo complete adequate colonoscopic examination preoperatively) should have a complete examination of the colon within 1 year after resection. If this or a complete preoperative examination is normal, subsequent examination should be offered after 3 years and then, if normal, every 5 years.

USPSTF
(1996)

Refer to specialist for regular endoscopic screening, diagnosis and management.

ACS
(2001)

Individuals with a personal history of curative-intent resection of colorectal cancer are at increased risk. Colonoscopy* is recommended within 1 year after resection. If normal, repeat examination in 3 years; if normal then, repeat examination every 5 years.

*Note: If a colonoscopy is not available, not feasible, or not desired by the patient, a DCBE, or flexible sigmoidoscopy followed by a DCBE can be used.

ICSI
(2000)

Patients at increased risk of developing colorectal cancer require colonoscopic surveillance at a 3 to 5 year interval, and are outside the scope of this guideline.

CTFPHC
(2001)

People with a history of colorectal cancer are beyond the scope of the guideline.

 

People with inflammatory bowel disease

AGA
(October, 1997)

Surveillance colonoscopy, looking for dysplasia as a marker of colorectal cancer risk, should be considered along with the extent and duration of the disease as a guide to when or if colectomy should be considered.

USPSTF
(1996)

Refer to specialist for regular endoscopic screening, diagnosis and management.

ACS
(2001)

Individuals with inflammatory bowel disease, chronic ulcerative colitis, or Crohn’s disease are at high risk. Colonoscopies with biopsies for dysplasia are recommended 8 years after the start of pancolitis; 12-15 years after the start of left-sided colitis. Examination should be repeated every 1-2 years. These patients are best referred to a center with experience in the surveillance and management of inflammatory bowel disease.

ICSI
(2000)

Patients at increase risk of developing colorectal cancer require colonoscopic surveillance at a 3 to 5 year interval, and are outside the scope of this guideline.

CTFPHC
(2001)

People with inflammatory bowel disease are beyond the scope of the guideline.

EVIDENCE RATING SCHEMES

 

Rating Scheme

USPSTF
(1996)

Levels of Evidence
In grading the quality of evidence, the Task Force gave greater weight to those study designs that, for methodologic reasons, are less subject to bias and inferential error. The following rating system was used:

I: Evidence obtained from at least one properly randomized controlled trial.
II-1: Evidence obtained from well-designed controlled trials without randomization.
II-2: Evidence obtained from well-designed cohort or case-control analytic studies, preferably from more than one center or research group.
II-3: Evidence obtained from multiple time series with or without the intervention. Dramatic results in uncontrolled experiments (such as the results of the introduction of penicillin treatment in the 1940s) could also be regarded as this type of evidence.
III: Opinions of respected authorities, based on clinical experience; descriptive studies and case reports; or reports of expert committees.

Well-designed and well-conducted meta-analyses were also considered, and were graded according to the quality of the studies on which the analyses were based (e.g., Grade I if the meta-analysis pooled properly randomized controlled trials).

Recommendation Grade
The strength of the recommendation for or against a preventive intervention was graded as follows:

A: There is good evidence to support the recommendation that the condition be specifically considered in a periodic health examination.
B: There is fair evidence to support the recommendation that the condition be specifically considered in a periodic health examination.
C: There is insufficient evidence to recommend for or against the inclusion of the condition in a periodic health examination, but recommendations may be made on other grounds.
D: There is fair evidence to support the recommendation that the condition be excluded from consideration in a periodic health examination.
E: There is good evidence to support the recommendation that the condition be excluded from consideration in a periodic health examination.

ICSI
(2000)

Evidence Grading System: Classes of Research Reports

A. Primary Reports of New Data Collection:

   Class A

  • Randomized, controlled trial

   Class B

  • Cohort study

   Class C

  • Non-randomized trial with concurrent or historical controls
  • Case-control study
  • Study of sensitivity and specificity of a diagnostic test
  • Population-based descriptive study

   Class D

  • Cross-sectional study
  • Case series
  • Case report

B. Reports that Synthesize or Reflect upon Collections of Primary Reports

   Class M

  • Meta-analysis
  • Decision analysis
  • Cost-benefit analysis
  • Cost-effectiveness study

   Class R

  • Review article
  • Consensus statement
  • Consensus report

   Class X

  • Medical opinion

CTFPHC
(2001)

Level of Evidence:

I - Evidence from at least 1 properly randomized controlled trial (RCT).
II-1 - Evidence from well-designed controlled trials without randomization.
II-2 - Evidence from well-designed cohort or case-control analytic studies, preferably from more than 1 centre or research group.
II-3 - Evidence from comparisons between times or places with or without the intervention. Dramatic results in uncontrolled experiments could also be included here.
III - Opinions of respected authorities, based on clinical experience, descriptive studies or reports of expert committees.

Recommendation Grade:

A. Good evidence to support the recommendation that the condition or manoeuvre be specifically considered in a periodic health examination (PHE).
B. Fair evidence to support the recommendation that the condition or manoeuvre be specifically considered in a periodic health examination.
C. Insufficient evidence regarding inclusion or exclusion of the condition or manoeuvre in a periodic health examination, but recommendations may be made on other grounds.
D. Fair evidence to support the recommendation that the condition or manoeuvre be specifically excluded from consideration in a periodic health examination.
E. Good evidence to support the recommendation that the condition or manoeuvre be specifically excluded from a periodic health examination.

 

GUIDELINE CONTENT COMPARISON

The American Gastroenterological Association (AGA), the U.S. Preventive Services Task Force (USPSTF), the American Cancer Society (ACS), the Institute for Clinical Systems Improvement (ICSI), and the Canadian Task Force on Preventive Health Care (CTFPHC) present recommendations for screening for colorectal cancer in people at average risk (asymptomatic, age > 50 years, no other risk factors) and provide explicit reasoning behind their judgments. The AGA, ACS, and CTFPHC also present screening recommendations for individuals at increased risk of colorectal cancer. Because the USPSTF and ICSI guidelines are intended for primary care clinicians and surveillance of high-risk populations requires referral to a specialist, further recommendations are not offered for these high-risk groups by the USPSTF and ICSI.

Areas of Agreement

The AGA, USPSTF, ACS, ICSI, and CTFPHC agree that asymptomatic adults > 50 years, with no other risk factors, should be screened for colorectal cancer, utilizing one of several acceptable screening tests such as fecal occult blood testing or flexible sigmoidoscopy. All five groups present two or more acceptable screening options and do not explicitly recommend one screening test over another. The ACS suggests that, whenever possible, patients participate in a shared decision-making process, where information about each of the screening options, such as accuracy, cost, potential for prevention, discomfort and risk is discussed. Similarly, the AGA concludes that decisions about which test or tests to use should take into account the patient’s preferences, the patient’s age, any existing comorbidity, and local resources and expertise. The USPSTF also recommends consideration of patient preferences and patient education in decision making rather than a uniform policy for all patients.

Due to several obstacles in the shared decision-making approach, such as availability of well trained personnel and the time it takes to explain options to patients, ACS acknowledges that clinicians may be able to successfully implement only one or two of the screening modalities, limiting options for patients. Consequently, ACS notes that of primary importance at this time is that clinicians recommend at least one of the appropriate screening options for all of their eligible patients.

The organizations acknowledge that the option of total colon examination (TCE) by colonoscopy or barium enema has not been supported by randomized controlled trials. Consequently, the USPSTF and CTFPHC do not recommend for or against colonoscopy, and USPSTF does not recommend for or against barium enema in asymptomatic individuals at average risk of colorectal cancer. CTFPHC did not consider screening with barium enema because of the lack of direct evidence. The AGA concluded total colon examination (TCE) by colonoscopy or barium enema were supported by indirect evidence, including the panel’s decision analysis conducted to investigate the clinical consequences of screening over time, despite the absence of direct evidence. ACS also cites compelling indirect evidence for benefit and efficacy of TCE. Consequently, the AGA, ACS and ICSI concluded that TCE by colonoscopy or barium enema is an acceptable screening option.

Areas of Differences

Although all the organizations share the fundamental recommendation for screening asymptomatic adults at average risk of colorectal cancer, there are subtle differences in what they propose as optimal screening measures. A difference between the ACS and the other groups concerns the recommendations for FOBT and sigmoidoscopy. Although ACS and the other groups recommend annual FOBT or flexible sigmoidoscopy every five years as acceptable screening options, ACS notes that annual FOBT accompanied by flexible sigmoidoscopy (every five years) is preferable to utilization of either test alone. AGA and ICSI also recommend the combination of FOBT and flexible sigmoidoscopy as a screening option; however, ACS is the only organization to advocate the combination strategy as the preferred approach (over either test alone). USPSTF and CTFPHC concluded there is insufficient evidence to determine whether this combination of tests produces greater benefits than either test alone.

Although all of the groups recommend screening with FOBT, CTFPHC is the only group that does not specifically recommend annual testing. However, they support screening in the periodic health examination of asymptomatic patients over age 50 with no other risk factors.

Screening recommendations for people with a family history of colorectal cancer vary among guidelines. AGA, USPSTF, ACS, and ICSI recommend increased surveillance or earlier screening for these individuals. In contrast, CTFPHC recommends that people with a family history of colorectal cancer or polyps undergo the same screening as average risk individuals, stating insufficient evidence to recommend colonsocopy for these individuals, unless the criteria for hereditary non-polyposis colon cancer is met. Although CTFPHC acknowledges that there is evidence of an increased prevalence of neoplasms in these individuals, there is insufficient information to recommend more intense screening than that of individuals at average risk.

Although there is general agreement among AGA, ACS, and CTFPHC regarding the need for genetic counseling in individuals at risk for familial adenomatous polyposis, CTFPHC is the only guideline to firmly recommend genetic testing. The Task Force for the CTFPHC recommends genetic testing of individuals at risk for familial adenematous polyposis if the genetic mutation has been identified in the family and if genetic testing is available. This recommendation is based on fair evidence to support the recommendation that the manoeuvre be specifically considered in a periodic health examination. USPSTF and ICSI do not comment on genetic counseling/screening as it is beyond the scope of their guidelines.

Updates in Progress: A third USPSTF was appointed in September 1998 by the Agency for Health Care Policy and Research (now known as the Agency for Healthcare Research and Quality [AHRQ]). USPSTF recommendations from the 2nd edition will be updated on an individual basis and new topics evaluated. Reviews and recommendations will be released as they are completed. This particular USPSTF guideline is currently under revision and is scheduled for release in 2002.

 

 

Edward E. Rylander, M.D.

Diplomat American Board of Family Practice.

Diplomat American Board of Palliative Medicine.