Colorectal cancer secondary prevention: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Colon cancer}} | {{Colon cancer}} | ||
To view the secondary prevention of familial adenomatous polyposis (FAP), click [[Familial adenomatous polyposis secondary prevention|'''here''']]<br> | |||
To view the secondary prevention of hereditary nonpolyposis colorectal cancer (HNPCC), click [[Hereditary nonpolyposis colorectal cancer secondary prevention|'''here''']]<br><br> | |||
{{CMG}} {{AE}} Saarah T. Alkhairy, M.D. | |||
==Overview== | ==Overview== | ||
Secondary prevention of colorectal cancer, as opposed to primary prevention, indicates that a person has already had the disease and there are steps being taken to prevent cancer recurrence, usually as metachronous tumors. This involves annual surveillance with colonoscopy after surgical removal an possibly an adjunct after the initial operation. The timing for secondary prevention is critical to prevent recurrent advanced disease<ref name="Carethers2010">{{cite journal|last1=Carethers|first1=John M.|title=Secondary Prevention of Colorectal Cancer: Is There an Optimal Follow-up for Patients with Colorectal Cancer?|journal=Current Colorectal Cancer Reports|volume=6|issue=1|year=2010|pages=24–29|issn=1556-3790|doi=10.1007/s11888-009-0038-1}}</ref>. | |||
==Colorectal Cancer Secondary Prevention== | |||
===Familial Colorectal Cancer Syndromes=== | |||
*Surgical resection followed by a colonoscopy yearly for most polyposis syndromes | |||
:*Criteria for surveilling patients and categorizing them as polyposis patients include | |||
::*The presence of multiple polyps in the colon | |||
::*Young age at onset of colorectal cancer, particularly age less than 50 years | |||
::*A strong family history suggesting a familial syndrome | |||
::*Evidence for a syndrome based on genetic testing | |||
*Chemoprevention has been used as an adjunct to colonoscopy in some FAP patients, such as cyclooxygenase (COX) inhibitors | |||
===Sporadic Colorectal Cancer Syndromes=== | |||
*An individual may develop sporadic colorectal cancer for the following reasons: | |||
:*The patient has an unrecognized familial syndrome | |||
:*The residual tumor may be present after resection | |||
:*The patient has strong risk factors | |||
:*The patient has genetic risk factors that do not fit into a familial syndrome | |||
*After diagnosis, a colonoscopy should be performed to rule out synchronous tumors and polyps | |||
*A primary tumor resection should be performed | |||
*Within 1 year after the primary tumor resection, another colonoscopy should take place | |||
:*If this examination is negative for lesions, the next colonoscopy generally may be performed after 3 years | |||
:*If that colonoscopy is negative, then secondary prevention by colonoscopy may be extended to every 5 years | |||
==References== | ==References== | ||
Revision as of 15:45, 15 July 2015
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To view the secondary prevention of familial adenomatous polyposis (FAP), click here
To view the secondary prevention of hereditary nonpolyposis colorectal cancer (HNPCC), click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Saarah T. Alkhairy, M.D.
Overview
Secondary prevention of colorectal cancer, as opposed to primary prevention, indicates that a person has already had the disease and there are steps being taken to prevent cancer recurrence, usually as metachronous tumors. This involves annual surveillance with colonoscopy after surgical removal an possibly an adjunct after the initial operation. The timing for secondary prevention is critical to prevent recurrent advanced disease[1].
Colorectal Cancer Secondary Prevention
Familial Colorectal Cancer Syndromes
- Surgical resection followed by a colonoscopy yearly for most polyposis syndromes
- Criteria for surveilling patients and categorizing them as polyposis patients include
- The presence of multiple polyps in the colon
- Young age at onset of colorectal cancer, particularly age less than 50 years
- A strong family history suggesting a familial syndrome
- Evidence for a syndrome based on genetic testing
- Chemoprevention has been used as an adjunct to colonoscopy in some FAP patients, such as cyclooxygenase (COX) inhibitors
Sporadic Colorectal Cancer Syndromes
- An individual may develop sporadic colorectal cancer for the following reasons:
- The patient has an unrecognized familial syndrome
- The residual tumor may be present after resection
- The patient has strong risk factors
- The patient has genetic risk factors that do not fit into a familial syndrome
- After diagnosis, a colonoscopy should be performed to rule out synchronous tumors and polyps
- A primary tumor resection should be performed
- Within 1 year after the primary tumor resection, another colonoscopy should take place
- If this examination is negative for lesions, the next colonoscopy generally may be performed after 3 years
- If that colonoscopy is negative, then secondary prevention by colonoscopy may be extended to every 5 years
References
- ↑ Carethers, John M. (2010). "Secondary Prevention of Colorectal Cancer: Is There an Optimal Follow-up for Patients with Colorectal Cancer?". Current Colorectal Cancer Reports. 6 (1): 24–29. doi:10.1007/s11888-009-0038-1. ISSN 1556-3790.