From the Guidelines
Patients with Inflammatory Bowel Disease (IBD) have a significantly increased risk of developing colorectal cancer, with a cumulative risk of 1%, 2%, and 5% after 10,20, and >20 years from an initial IBD diagnosis, respectively, as reported in a recent meta-analysis 1.
Incidence of Colon Cancer in IBD Patients
The incidence of colon cancer in patients with IBD is a significant concern, with chronic colonic inflammation being a direct consequence of the disease.
- The risk of colorectal cancer (CRC) in IBD patients is attributed to chronic inflammation causing DNA damage, promoting cellular proliferation, and creating an environment conducive to malignant transformation.
- The cumulative risk of CRC in IBD patients has been reported to be 1%, 2%, and 5% after 10,20, and >20 years from an initial IBD diagnosis, respectively 1.
- The risk is particularly elevated in patients with extensive colitis, longer disease duration, primary sclerosing cholangitis, family history of colorectal cancer, and persistent inflammation.
Surveillance and Screening
Due to the elevated risk of CRC in IBD patients, regular surveillance colonoscopies with multiple biopsies are essential for improving outcomes in these high-risk patients.
- The British Society of Gastroenterology consensus guidelines recommend commencement of surveillance endoscopy for dysplasia in IBD to begin at between 6 and 10 years following diagnosis 1.
- Patients with primary sclerosing cholangitis (PSC) should have annual surveillance colonoscopy from diagnosis, while others should begin surveillance 8 years after diagnosis or after the onset of symptoms if there was a significant delay before diagnosis 1.
Importance of Early Detection
Early detection through surveillance colonoscopies is crucial for improving outcomes in IBD patients with CRC.
- A study of 149 IBD-associated cancers showed that those with prior surveillance had greater 5-year survival and earlier tumor stage at detection 1.
- The use of chromoendoscopy and targeted biopsies can increase the detection rate of CRC in IBD patients, especially in those with PSC-IBD 1.
From the Research
Incidence of Colon Cancer in Patients with Inflammatory Bowel Disease
The incidence of colon cancer in patients with inflammatory bowel disease (IBD) is a significant concern, with various studies highlighting the increased risk of colorectal cancer (CRC) in these patients.
- Patients with IBD are at significantly increased risk of CRC, principally resulting from the pro-neoplastic effects of chronic intestinal inflammation 2.
- The incidence of CRC in IBD patients has declined over the past 30 years, attributed to both successful CRC-surveillance programs and improved control of mucosal inflammation 2.
- Risk factors that further increase the risk of IBD-related CRC include disease duration, extent and severity, the presence of inflammatory pseudopolyps, coexistent primary sclerosing cholangitis, and a family history of CRC 2.
Surveillance and Detection
Surveillance and detection of CRC in IBD patients are crucial for early detection and prevention of neoplasia.
- High-definition endoscopy systems and chromoendoscopy can provide increased contrast and improved detection of dysplastic lesions 3, 4.
- International specialty society guidelines differ in their recommendations regarding use of chromoendoscopy for dysplasia surveillance, with some guidelines advocating a risk-stratified surveillance strategy 3.
- Longitudinal data showing a benefit in morbidity or mortality from the use of chromoendoscopy are still lacking 4.
Epidemiology and Prognosis
The epidemiology and prognosis of IBD-related CRCs are important considerations.
- IBD-related CRC is responsible for approximately 2% of the annual mortality from CRC overall, but 10-15% of the annual deaths in IBD patients 5.
- IBD-related CRC patients are also affected at a younger age than sporadic CRC patients, and have a 5-year survival rate of 50% 5.
- Patients with IBD-related CRCs exhibit a poorer prognosis than those with sporadic CRCs, owing to their aggressive histological characteristics and lower curative resection rate 6.