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| | __NOTOC__ |
| | {{Colon cancer}} |
| | To view familial adenomatous polyposis (FAP), click [[Familial adenomatous polyposis|'''here''']]<br> |
| | To view hereditary nonpolyposis colorectal cancer (HNPCC), click [[Hereditary nonpolyposis colorectal cancer|'''here''']]<br><br> |
| '''For patient information click [[{{PAGENAME}} (patient information)|here]]''' | | '''For patient information click [[{{PAGENAME}} (patient information)|here]]''' |
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| {{DiseaseDisorder infobox | | | {{CMG}}; {{AE}} Saarah T. Alkhairy, M.D |
| Name = Colorectal cancer |
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| ICD10 = {{ICD10|C|18||c|15}}-{{ICD10|C|20||c|15}} |
| | {{SK}} Colon cancer; bowel cancer |
| ICD9 = {{ICD9|153.0}}-{{ICD9|154.1}} |
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| ICDO = {{ICDO|8140|3}} (95% of cases) |
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| OMIM = 114500 |
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| OMIM_mult = |
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| MedlinePlus = 000262 |
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| DiseasesDB = 2975 |
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| }}
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| {{Colon cancer}}
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| '''Editor(s)-in-Chief:''' [[C. Michael Gibson]], M.S.,M.D. [mailto:mgibson@perfuse.org] Phone:617-632-7753; Elliot B. Tapper, M.D., Beth Israel Deaconess Medical Center
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| ==[[Colorectal cancer overview|Overview]]== | | ==[[Colorectal cancer overview|Overview]]== |
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| ==[[Colorectal cancer history and symptoms|History & Symptoms]]== | | ==[[Colorectal cancer historical perspective|Historical Perspective]]== |
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| ==[[Colorectal cancer risk factors|Risk factors]]==
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| ==[[Colorectal cancer screening|Screening]] ==
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| == Diagnosis ==
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| :[[Colorectal cancer history and symptoms| History and Symptoms]] | [[Colorectal cancer physical examination | Physical Examination]] | [[Colorectal cancer staging | Staging]] | [[Colorectal cancer laboratory studies | Lab Studies]] | [[Colorectal cancer electrocardiogram|Electrocardiogram]] | [[Colorectal cancer x ray|X Ray]] | [[Colorectal cancer MRI|MRI]] | [[Colorectal cancer CT|CT]] | [[Colorectal cancer echocardiography|Echocardiography]] | [[Colorectal cancer other imaging findings|Other imaging findings]]
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| ==[[Colorectal cancer pathophysiology|Pathophysiology]]== | | ==[[Colorectal cancer pathophysiology|Pathophysiology]]== |
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| ==Treatment== | | ==[[Colorectal cancer causes|Causes]]== |
| The treatment depends on the staging of the cancer. When colorectal cancer is caught at early stages (with little spread) it can be curable. However when it is detected at later stages (when distant [[metastasis|metastases]] are present) it is less likely to be curable.
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| [[Colorectal cancer medical therapy|Medical therapy]] | [[Colorectal cancer surgery|Surgical options]] | [[Colorectal cancer primary prevention|Primary prevention]] | [[Colorectal cancer secondary prevention|Secondary prevention]] | [[Colorectal cancer cost-effectiveness of therapy|Financial costs]] | [[Colorectal cancer future or investigational therapies|Future therapies]] | | ==[[Colorectal cancer differential diagnosis|Differentiating Colorectal cancer from other Diseases]]== |
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| ===Vaccine=== | | ==[[Colorectal cancer epidemiology and demographics|Epidemiology and Demographics]]== |
| In November 2006, it was announced that a [[vaccine]] had been developed and tested with very promising results.<ref>[http://www.dailymail.co.uk/pages/live/articles/news/news.html?in_article_id=416006&in_page_id=1770 Wheldon, Julie. Vaccine for kidney and bowel cancers 'within three years' ''The Daily Mail'' [[2006-11-13]]]]</ref> The new vaccine, called [[TroVax]], works in a totally different way to existing treatments by harnessing the patient's own immune system to fight the disease. Experts say this suggests that [[gene therapy]] vaccines could prove an effective treatment for a whole range of cancers. [http://www.oxfordbiomedica.co.uk/ Oxford BioMedica] is a British spin-out from Oxford University specializing in the development of gene-based treatments. Phase III trials are underway for renal cancers and planned for colon cancers.<ref>[http://www.medscape.com/viewarticle/561321?src=mp Vaccine Works With Chemotherapy in Colorectal Cancer (Reuters) [[2007-08-13]]]</ref>
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| ===Treatment of colorectal cancer metastasis to the liver=== | | ==[[Colorectal cancer risk factors|Risk factors]]== |
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| According to the American Cancer Society statistics in 2006 [http://www.cancer.org/docroot/PRO/content/PRO_1_1_Cancer_Statistics_2006_Presentation.asp]greater than 20% of patients present with metastatic (stage IV) colorectal cancer at the time of diagnosis, and up to 25% of this group will have isolated liver metastasis that is potentially resectable. Lesions which undergo curative resection have demonstrated 5-year survival outcomes now exceeding 50%.<ref> Simmonds PC, et al. Surgical Resection of hepatic metastasis from colorectal cancer: A systemic review of published studies. Br J Surg. 2006;94:982-999. PMID 16538219 </ref>
| | ==[[Colorectal cancer screening|Screening]] == |
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| Resectability of a liver met is determined using preoperative imaging studies (Ct or MRI), intraoperative ultrasound, and by direct palpation and visualization during resection. Lesions confined to the right lobe are amenable to en bloc removal with a right hepatectomy (liver resection) surgery. Smaller lesions of the central or left liver lobe may sometimes be resected in anatomic "segments", while large lesions of left hepatic lobe are resected by a procedure called hepatic trisegmentectomy. Treatment of lesions by smaller,non-anatomic "wedge" resections is associated with higher recurrence rates. Some lesions which are not initially amenable to surgical resection may become candidates if they have significant responses to preoperative chemotherapy or immunotherapy regimines. Lesions which are not amenable to surgical resection for cure can be treated with modalities including radio-frequency ablation (RFA), cryoablation, and chemoembolization.
| | ==[[Colorectal cancer natural history|Natural History, Complications and Prognosis]]== |
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| Patients with colon cancer and metastatic disease to the liver may be treated in either a single surgery or in staged surgeries (with the colon tumor traditionally removed first) depending upon the fitness of the patient for prolonged surgery, the difficulty expected with the procedure with either the colon or liver resection, and the comfort of the surgery performing potentially complex hepatic surgery.
| | == Diagnosis == |
| | [[Colorectal cancer staging|Staging]] | [[Colorectal cancer history and symptoms|History and Symptoms]] | [[Colorectal cancer physical examination|Physical Examination]] | [[Colorectal cancer laboratory tests|Laboratory Findings]] | [[Colorectal cancer x ray|X Ray]] | [[Colorectal cancer MRI|MRI]] | [[Colorectal cancer CT|CT]] | [[Colorectal cancer ultrasound|Ultrasound]] | [[Colorectal cancer other imaging findings|Other Imaging Findings]] | [[Colorectal cancer other diagnostic studies|Other Diagnostic Studies]] |
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| Poor pronostic factors of patients with liver metastasis include
| | ==Treatment== |
| * Synchronous (diagnosed simultaneously) liver and primary colorectal tumors
| | [[Colorectal cancer medical therapy|Medical Therapy]] | [[Colorectal cancer surgery|Surgery]] | [[Colorectal cancer metastasis treatment|Metastasis Treatment]] | [[Colorectal cancer primary prevention|Primary prevention]] | [[Colorectal cancer secondary prevention|Secondary prevention]] | [[Colorectal cancer follow up|Follow-up]] | [[Colorectal cancer cost-effectiveness of therapy|Cost-Effectiveness of Therapy]] | [[Colorectal cancer future or investigational therapies|Future or Investigational Therapies]] |
| * A short time between detecting the primary cancer and subsequent development of liver mets
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| * Multiple metastatic lesions
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| * High blood levels of the tumor marker, carcino-embryonic antigen ('''CEA'''), in the patient prior to resection
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| * Larger size metastatic lesions
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| ==Prognosis==
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| Survival is directly related to detection and the type of cancer involved. Survival rates for early stage detection is about 5 times that of late stage cancers. CEA level is also directly related to the prognosis of disease, since its level correlates with the bulk of tumor tissue.
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| ==Follow-up== | |
| The aims of follow-up are to diagnose in the earliest possible stage any metastasis or tumors that develop later but did not originate from the original cancer (metachronous lesions).
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| The U.S. [[National Comprehensive Cancer Network]] and [[American Society of Clinical Oncology]] provide guidelines for the follow-up of colon cancer.<ref name="NCCNguidelines">[http://www.nccn.org/professionals/physician_gls/PDF/colon.pdf NCCN Clinical Practice Guidelines in Oncology - Colon Cancer (version 1, 2008: September 19, 2007).]</ref><ref name="ASCOguidelines">{{cite journal |last=Desch CE, Benson AB 3rd, Somerfield MR, ''et al''; American Society of Clinical Oncology |first= |authorlink= |coauthors= |year=2005 |month= |title=Colorectal cancer surveillance: 2005 update of an American Society of Clinical Oncology practice guideline |journal=J Clin Oncol |volume=23 |issue=33 |pages=8512-9 |id= |url=http://jco.ascopubs.org/cgi/reprint/JCO.2005.04.0063v1.pdf |accessdate= |quote= }}</ref> A [[medical history]] and [[physical examination]] are recommended every 3 to 6 months for 2 years, then every 6 months for 5 years. [[Carcinoembryonic antigen]] blood level measurements follow the same timing, but are only advised for patients with T2 or greater lesions who are candidates for intervention. A [[Computed tomography|CT-scan]] of the chest, abdomen and pelvis can be considered annually for the first 3 years for patients who are at high risk of recurrence (for example, patients who had poorly differentiated tumors or venous or lymphatic invasion) and are candidates for curative surgery (with the aim to cure). A [[colonoscopy]] can be done after 1 year, except if it could not be done during the initial staging because of an obstructing mass, in which case it should be performed after 3 to 6 months. If a villous polyp, polyp >1 centimeter or high grade dysplasia is found, it can be repeated after 3 years, then every 5 years. For other abnormalities, the colonoscopy can be repeated after 1 year.
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| Routine [[Positron emission tomography|PET]] or [[Medical ultrasonography|ultrasound scanning]], [[chest X-ray]]s, [[complete blood count]] or [[liver function tests]] are not recommended.<ref name="NCCNguidelines"/><ref name="ASCOguidelines"/> These guidelines are based on recent meta-analyses showing that intensive surveillance and close follow-up can reduce the 5-year mortality rate from 37% to 30%.<ref name="Cochrane2002">{{cite journal |last=Jeffery M, Hickey BE, Hider PN|first=|authorlink= |coauthors=|year=2002 |month= |title=Follow-up strategies for patients treated for non-metastatic colorectal cancer |journal=Cochrane Database Syst Rev |volume= |issue= |pages= |id=CD002200 |url=http://mrw.interscience.wiley.com/cochrane/clsysrev/articles/CD002200/frame.html |accessdate= |quote= }}</ref><ref name="BMJfollowup">{{cite journal |last=Renehan AG, Egger M, Saunders MP, O'Dwyer ST|first= |authorlink= |coauthors= |year=2002 |month= |title=Impact on survival of intensive follow up after curative resection for colorectal cancer: systematic review and meta-analysis of randomised trials |journal=BMJ |volume=324 |issue=7341 |pages=831-8 |id= |url=http://www.bmj.com/cgi/reprint/324/7341/813 |accessdate= |quote= }}</ref><ref name="BMCCancerFollowup">{{cite journal |last=Figueredo A, Rumble RB, Maroun J, ''et al''; Gastrointestinal Cancer Disease Site Group of Cancer Care Ontario's Program in Evidence-based Care. |first= |authorlink= |coauthors= |year=2003 |month= |title=Follow-up of patients with curatively resected colorectal cancer: a practice guideline. |journal=BMC Cancer |volume=3 |issue= |pages=26 |id= |url=http://www.biomedcentral.com/1471-2407/3/26 |accessdate= |quote= }}</ref>
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| ==Prevention==
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| Most colorectal cancers should be preventable, through increased surveillance, improved lifestyle, and, probably, the use of dietary chemopreventative agents.
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| ===Surveillance===
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| Most colorectal cancer arise from adenomatous polyps. These lesions can be detected and removed during [[colonoscopy]]. Studies show this procedure would decrease by > 80% the risk of cancer death, provided it is started by the age of 50, and repeated every 5 or 10 years.<ref>Winawer SJ, Zauber AG, Ho MN, O'Brien MJ, Gottlieb LS, Sternberg SS, Waye JD, Schapiro M, Bond JH, Panish JF, Ackroyd F, Shike M, Kurtz RC, Hornsby-Lewis L, Gerdes H, Stewart ET, The National Polyp Study Workgroup. ''Prevention of colorectal cancer by colonoscopic polypectomy.'' [[N Engl J Med]] 1993;329:1977-81. PMID 8247072.</ref>
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| As per current guidelines under [[National Comprehensive Cancer Network]], in average risk individuals with negative family history of colon cancer and personal history negative for [[adenomas]] or [[Inflammatory Bowel diseases]], flexible sigmoidoscopy every 5 years with fecal occult blood testing annually or double contrast barium enema are other options acceptable for screening rather than colonoscopy every 10 years (which is currently the Gold-Standard of care).
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| ===Lifestyle & Nutrition===
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| The comparison of colorectal cancer incidence in various countries strongly suggests that sedentarity, overeating (i.e., high caloric intake), and perhaps a diet high in meat (red or processed) could increase the risk of colorectal cancer. In contrast, a healthy body weight, physical fitness, and good nutrition decreases cancer risk in general. Accordingly, lifestyle changes could decrease the risk of colorectal cancer as much as 60-80%.<ref>{{cite journal|last=Cummings |first=JH |coauthors=Bingham SA |title=Diet and the prevention of cancer |journal=[[British Medical Journal|BMJ]] |year=1998|issue317|pages=1636-40 |url=http://bmj.bmjjournals.com/ |id=PMID 9848907}}</ref>
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| A high intake of dietary fiber (from eating fruits, vegetables, cereals, and other high fiber food products) has, until recently, been thought to reduce the risk of colorectal cancer and adenoma. In the largest study ever to examine this theory (88,757 subjects tracked over 16 years), it has been found that a fiber rich diet does not reduce the risk of colon cancer. <ref>{{cite journal |title=Dietary Fiber and the Risk of Colorectal Cancer and Adenoma in Women |journal=New England Journal of Medicine |year=1999 |issue=340 |pages=169-76 |url=http://content.nejm.org/cgi/content/full/340/3/169}}</ref> A 2005 meta-analysis study further supports these findings.<ref>{{cite journal |title=Dietary Fiber and Colorectal Cancer: An Ongoing Saga |journal=Journal of the American Medical Association |year=2005 |issue=294(22) |pages=2904 - 2906 |url=http://jama.ama-assn.org/cgi/content/extract/294/22/2904 |id=PMID 16352792}}</ref>
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| The Harvard School of Public Health states:
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| "Health Effects of Eating Fiber: Long heralded as part of a healthy diet, fiber appears to reduce the risk of developing various conditions, including heart disease, diabetes, diverticular disease, and constipation. Despite what many people may think, however, fiber probably has little, if any effect on colon cancer risk." <ref>{{cite web|title=Health Effects of Eating Fiber |url=http://www.hsph.harvard.edu/nutritionsource/fiber.html}}</ref>
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| ===Chemoprevention===
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| More than 200 agents, including the above cited phytochemicals, and other food components like calcium or folic acid (a B vitamin), and [[NSAID]]s like aspirin, are able to decrease carcinogenesis in preclinical models: Some studies show full inhibition of carcinogen-induced tumours in the colon of rats. Other studies show strong inhibition of spontaneous intestinal polyps in mutated mice (Min mice). Chemoprevention clinical trials in human volunteers have shown smaller prevention, but few intervention studies have been completed today. Calcium, aspirin and celecoxib supplements, given for 3 to 5 years after the removal of a polyp, decreased the recurrence of polyps in volunteers (by 15-40%). The "chemoprevention database" shows the results of all published scientific studies of chemopreventive agents, in people and in animals.<ref>{{cite web |url=http://www.inra.fr/reseau-nacre/sci-memb/corpet/indexan.html |title=Colorectal Cancer Prevention: Chemoprevention Database |accessdate=2007-08-23 |format= |work=}}</ref>
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| ====Aspirin chemoprophylaxis====
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| Aspirin should not be taken routinely to prevent colorectal cancer, even in people with a family history of the disease, because the risk of bleeding and kidney failure from high dose aspirin (300mg or more) outweigh the possible benefits.<ref>{{cite web |title=Task Force Recommends Against Use of Aspirin and Non-Steroidal Anti-Inflammatory Drugs to Prevent Colorectal Cancer |url=http://www.ahrq.gov/news/press/pr2007/aspnsaidpr.htm |author=Agency for Healthcare Research and Quality | accessdate=2007-05-07 |date=2007-03-05 |publisher=United States Department of Health & Human Services }}</ref>
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| A [[clinical practice guideline]] by the [http://www.ahrq.gov/clinic/uspstfix.htm U.S. Preventive Services Task Force (USPSTF)] recommended against taking [[aspirin]] ([http://www.ahrq.gov/clinic/3rduspstf/ratings.htm grade D recommendation]).<ref name="pmid17339621">{{cite journal |author= |title=Routine aspirin or nonsteroidal anti-inflammatory drugs for the primary prevention of colorectal cancer: U.S. Preventive Services Task Force recommendation statement |journal=Ann. Intern. Med. |volume=146 |issue=5 |pages=361-4 |year=2007 |id=pmid=17339621 |doi=}} PMID 17339621</ref> The Task Force acknowledged that aspirin may reduce the incidence of colorectal cancer, but "concluded that harms outweigh the benefits of aspirin and NSAID use for the prevention of colorectal cancer". A subsequent [[meta-analysis]] concluded "300 mg or more of aspirin a day for about 5 years is effective in primary prevention of colorectal cancer in randomised controlled trials, with a latency of about 10 years".<ref name="pmid17499602">{{cite journal |author=Flossmann E, Rothwell PM |title=Effect of aspirin on long-term risk of colorectal cancer: consistent evidence from randomised and observational studies |journal=Lancet |volume=369 |issue=9573 |pages=1603-13 |year=2007 |pmid=17499602 |doi=10.1016/S0140-6736(07)60747-8}} PMID 17499602</ref> However, long-term doses over 81 mg per day may increase bleeding events.<ref name="pmid17488967">{{cite journal |author=Campbell CL, Smyth S, Montalescot G, Steinhubl SR |title=Aspirin dose for the prevention of cardiovascular disease: a systematic review |journal=JAMA |volume=297 |issue=18 |pages=2018-24 |year=2007 |pmid=17488967 |doi=10.1001/jama.297.18.2018}} PMID 17488967</ref>
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| ====Calcium====
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| A [[meta-analysis]] by the [[Cochrane Collaboration]] of [[randomized controlled trials]] published through 2002 concluded "Although the evidence from two RCTs suggests that calcium supplementation might contribute to a moderate degree to the prevention of colorectal adenomatous polyps, this does not constitute sufficient evidence to recommend the general use of calcium supplements to prevent colorectal cancer.".<ref name="pmid16034903">{{cite journal |author=Weingarten MA, Zalmanovici A, Yaphe J |title=Dietary calcium supplementation for preventing colorectal cancer and adenomatous polyps |journal=Cochrane database of systematic reviews (Online) |volume= |issue=3 |pages=CD003548 |year=2005 |pmid=16034903 |doi=10.1002/14651858.CD003548.pub3}}</ref> Subsequently, one [[randomized controlled trial]] by the [[Women's Health Initiative]] (WHI) reported negative results.<ref name="pmid16481636">{{cite journal |author=Wactawski-Wende J, Kotchen JM, Anderson GL, ''et al'' |title=Calcium plus vitamin D supplementation and the risk of colorectal cancer |journal=N. Engl. J. Med. |volume=354 |issue=7 |pages=684-96 |year=2006 |pmid=16481636 |doi=10.1056/NEJMoa055222}}</ref> A second [[randomized controlled trial]] reported reduction in all cancers, but had insufficient colorectal cancers for analysis.<ref name="pmid17556697">{{cite journal |author=Lappe JM, Travers-Gustafson D, Davies KM, Recker RR, Heaney RP |title=Vitamin D and calcium supplementation reduces cancer risk: results of a randomized trial |journal=Am. J. Clin. Nutr. |volume=85 |issue=6 |pages=1586-91 |year=2007 |pmid=17556697 |doi=|url=http://www.ajcn.org/cgi/content/full/85/6/1586}}</ref>
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| ==Mathematical modeling== | | ==Case Studies== |
| Colorectal cancer has been for years subject of mathematical modeling.<ref>{{cite journal | author = van Leeuwen I, Byrne H, Jensen O, King J | title = Crypt dynamics and colorectal cancer: advances in mathematical modelling. | journal = Cell Prolif | volume = 39 | issue = 3 | pages = 157-81 | year = 2006 | id = PMID 16671995}}[http://www.maths.nottingham.ac.uk/personal/pmzivl/LeeuByrn2006.html Full text]</ref> For a comprehensive overview of current computational approaches on colorectal cancer see the [http://www.maths.nottingham.ac.uk/personal/pmzivl/crc.html Integrative Biology] web page.
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| ==References==
| | [[Colorectal cancer case study one|Case #1]] |
| {{Reflist|2}}
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| ==See also== | | ==Related Chapters== |
| * [[Hereditary nonpolyposis colorectal cancer]] | | * [[Hereditary nonpolyposis colorectal cancer]] |
| * [[Diet and cancer]] | | * [[Diet and cancer]] |
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| == External links == | | ==External Links== |
| *[http://www.cancer.gov/cancerinfo/wyntk/colon-and-rectum National Cancer Institute (Cancer.gov)] colorectal cancer
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| *[http://clinicaltrials.gov/ct/search?term=colorectal+cancer Current clinical trials] | | *[http://clinicaltrials.gov/ct/search?term=colorectal+cancer Current clinical trials] |
| *[http://nccam.nih.gov/clinicaltrials/colorectalcancer.htm Complementary medical clinical trials]
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| {{Gastroenterology}} | | {{Gastroenterology}} |
| {{Tumors}} | | {{Tumors}} |
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| [[ar:سرطان القولون]] | | [[ar:سرطان القولون]] |
| [[bs:Rak debelog crijeva]] | | [[bs:Rak debelog crijeva]] |
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| [[Category:Disease]] | | [[Category:Disease]] |
| [[Category:Gastroenterology]] | | [[Category:Gastroenterology]] |
| | [[Category:Oncology]] |
| [[Category:Types of cancer]] | | [[Category:Types of cancer]] |
| [[Category:Conditions diagnosed by stool test]] | | [[Category:Conditions diagnosed by stool test]] |
| [[Category:Mature chapter]] | | [[Category:Mature chapter]] |
| | [[Category:Up-To-Date]] |
| | [[Category:Medicine]] |
| | [[Category:Surgery]] |