Früherkennung von Darmkrebs durch Screening

Colorectal cancers are common, and early detection improves prognosis. See the separate Colorectal Cancer article.

Why is early detection important?¹

Early detection is important because the estimated lifetime risk of being diagnosed with bowel cancer is 1 in 15 (7%) for males, and 1 in 18 (6%) for females born after 1960 in the UK and early detection improves outcome.

Colorectal cancer is common and has significant mortality. In the UK:

• Bowel cancer is the 4th most common cancer in the UK, accounting for 11% of all new cancer cases (2016-2018).

• 52.9% of people diagnosed with bowel cancer in England survive their disease for ten years or more, it is predicted (2013-2017).

• Bowel cancer survival has more than doubled in the last 50 years in the UK.

• Early detection improves outcome.²

Early detection can be achieved by:

• Identifying those at risk. For example, the risk of colorectal cancer increases with age. 95% of cases occur in people aged over 50. Those with an affected first-degree relative have an 80% higher risk.³ Around 5% are associated with the genetic syndromes familial adenomatous polyposis (FAP) and hereditary non-polyposis colon cancer (HNPCC). These patients tend to present at a younger age. Those with inflammatory bowel disease have a 70% increased risk and risk increases with duration of the disease.⁴

• Case recognition through clinical awareness of the disease, including knowledge of those at risk, clinical presentations and when and how to refer.

• Screening programmes. Screening involves a national screening programme for patients without symptoms, and normal population risk, and targeted surveillance programmes for those who are at special risk (eg, inflammatory bowel disease or a strong family history).⁵

A national call and recall system with local hubs has been rolled out across the UK.⁶

Currently patients are sent faecal immunochemical test kits every 2 years. Local screening centres analyse samples, despatch results, provide endoscopy investigation services, specialist screening nurse clinics and, if necessary, referral to a local hospital multidisciplinary team (MDT) for people with abnormal results.

Men and women are screened every two years, which was initially between the ages of 60 to 74 in England, Wales and Northern Ireland, and between the ages of 50 to 74 in Scotland. The screening programme is now being expanded to include 50-74 year olds in England, Wales and Northern Ireland.

People with an age above the screening age group can request a screening kit by calling the freephone helpline unique to each country's programme. Details are available via the UK screening portal.⁶

Results obtained from the first three years of screening indicated that on average 1.9% of tests are positive (rates are slighter higher as age increases, in men and in Scotland). Cancer was identified in 1.62 per 1,000 people screened; of these, 48% were Dukes' stage A, and only 1% were found to have metastasised at diagnosis. Of those with a positive initial test, 10.9% will have a cancer and 35% an adenoma.⁷

In 2018 an independent expert screening committee recommended that bowel cancer screening in England should start 10 years earlier at age 50.⁸ Therefore, the programme is expanding so that everyone aged 50 to 59 years will also be eligible for screening. This is happening gradually over 4 years and started in April 2021 with 56 year olds. Following a thorough review of the evidence, the committee also recommended that screening should use the Stuhl-Immunochemischer Test (FIT). This test is easier to use than the previously used faecal occult blood test kit and is more accurate in detecting potential cancers.

The American Cancer Society (ACS) recommends that people who do not have an increased risk of colorectal cancer start regular screening at age 45.⁹ This can be done either with a stool-based test, or with a test that looks at the colon and rectum - bowel scope. People who are in good health with a life expectancy of more than 10 years should continue regular colorectal cancer screening through the age of 75. Between 76 and 85 years, the decision to be screened should be based on a person's preferences, life expectancy, overall health, and prior screening history. People over 85 should no longer get colorectal cancer screening.

These are more targeted screening programmes and protocols which select out sectors of the population at particularly high risk of colorectal carcinoma. These groups usually require endoscopic screening methods. High-risk groups include patients with:

• Previous resection of a kolorektales Karzinom.

• Previous colorectal adenomatous polyps (see below).

• Inflammatory bowel disease (see below).

• Ureterosigmoidostomy - annual flexible sigmoidoscopy beginning 10 years after the original operation.

• Akromegalie - regular colonoscopic screening from the age of 40 years:
  

  • Patients with an adenoma at first screening or elevated IGF-1 level should be offered three-yearly screening.

  • The remainder should be offered screening colonoscopy every 5-10 years.

• Family history of colorectal cancer. Patients with a personal or close family history (first-degree relative) consistent with an autosomal dominant cancer syndrome or a characterised polyposis syndrome should be referred for assessment, genetic counselling and mutation analysis. High-risk patients are first-degree relatives (where the patient developed cancer aged <50). These genetic conditions are:
  

  • HNPCC, or Lynch's syndrome - colonoscopy every two years from the age of 25 until the number of polyps make prophylactic colectomy advisable. Upper gastrointestinal (GI) endoscopy every two years from the age of 50.

  • FAP - usually requires prophylactic colectomy between the ages of 16 and 25 years. Upper GI endoscopy surveillance three-yearly from the age of 30.

  • MUTYH-associated polyposis (MAP) - colonoscopy every 2-3 years from the age of 25, upper GI endoscopy every 3-5 years from the age of 30.

  • Juvenile polyposis - colonoscopy every 18-24 months from the age of 18 (or earlier if there are any symptoms) and upper GI endoscopy every 1-2 years from the age of 25.

  • Peutz-Jeghers syndrome - two-yearly colonoscopy and upper GI endoscopy from the age of 25.

Recommendations for screening protocols for individuals identified as having moderate-to-high risk or low-to-moderate risk are complex - see the British Society of Gastroenterology (BSG) guideline.⁵

Adenomas

• Low risk (one or two adenomas smaller than 10 mm):
  

  • Consider colonoscopy after five years.

• Intermediate risk (three or four adenomas smaller than 10 mm, oder one or two adenomas if one is 10 mm or larger):
  

  • Offer colonoscopy after three years.

• High risk (2 or more premalignant polyps including at least one advanced colorectal polyp [defined as a serrated polyp of at least 10mm in size or containing any grade of dysplasia, or an adenoma of at least 10mm in size or containing high-grade dysplasia]; or 5 or more premalignant polyps:

  • One-off surveillance colonoscopy at 3 years.

• Post-colorectal cancer-resection patients should undergo a 1-year clearance colonoscopy, then a surveillance colonoscopy after 3 more years.

Entzündliche Darmerkrankung

• Colonoscopic surveillance should be offered to people whose symptoms started 10 years previously and who have Colitis ulcerosa (but not proctitis alone) or Morbus Crohn Kolitis involving more than one segment of colon.

• Offer a baseline colonoscopy with chromoscopy and targeted biopsy of any abnormal areas to determine the risk of developing colorectal cancer:
  

  • Low risk (left-sided ulcerative colitis or Crohn's colitis, oder extensive but quiescent ulcerative colitis oder extensive but quiescent Crohn's colitis):
    

    • Offer further colonoscopy with chromoscopy after five years.

  • Intermediate risk (extensive ulcerative or Crohn's colitis with mild active inflammation confirmed endoscopically or histologically, oder post-inflammatory polyps, oder family history of colorectal cancer in a first-degree relative aged 50 or over):
    

    • Offer further colonoscopy with chromoscopy after three years.

  • High risk (extensive ulcerative or Crohn's colitis with moderate or severe active inflammation confirmed endoscopically or histologically, oder Primäre sklerosierende Cholangitis (including after liver transplant), oder colonic stricture in the preceding five years, oder any grade of dysplasia in the preceding five years, oder family history of colorectal cancer in a first-degree relative aged under 50):
    

    • Offer further colonoscopy with chromoscopy after one year.