Colon Cancer: The Basics
Carolyn Vachani, RN, MSN, AOCN
Updated by: Elizabeth Prechtel-Dunphy, MSN, CRNP
The Abramson Cancer Center of the University of Pennsylvania
Last Modified: February 12, 2015
What is the colon?
The colon is the longest portion of the large intestine, also known as the large bowel. The large intestine is the last part of the digestive tract. It is a tube that is about 5 to 6 feet in length; the first 5 feet make up the colon, which then connects to about 6 inches of rectum, and finally ends with the anus. By the time food reaches the colon (about 3 to 8 hours after eating), the nutrients have been absorbed and the remainder is liquid waste product. The colon's function is to change this liquid waste into solid stool. The stool can spend anywhere from 10 hours to several days in the colon before being expelled through the anus. It has been suggested that the longer stool remains in the colon, the higher the risk for colon cancer, but this has not been proven.
What is colon cancer?
Colon cancer is malignant tissue that grows in the wall of the colon. The majority of tumors begin when normal tissue in the colon wall forms an adenomatous polyp, or pre-cancerous growth projecting from the colon wall. As this polyp grows larger, the tumor is formed. This process can take many years, which allows time for early detection with screening tests.
Am I at Risk for Colon Cancer?
Colon cancer is the third most common type of cancer, in both males and females, in the Western world. The incidence is highest in African Americans, who are also more likely to die of the disease. Certain factors put people at higher risk. It is estimated that in the United States in 2015 there will 93,090 new case and 49,700 deaths related to colon cancer. The risk of colon cancer rises substantially after age 50, but every year there are numerous cases reported in younger people. Individuals with a personal or family history of colon cancer, polyps, or inherited colon cancer syndromes (i.e., FAP and HNPCC), as well as patients with ulcerative colitis or Crohn's disease, are all at higher risk and may require screening at an earlier age than the general population. A person with one first degree relative (parent, sibling or child) with colon cancer is 2 to 3 times as likely to develop the cancer as someone who does not have an affected relative.
However, this does not mean that people without a family history are not at risk. In fact, about 80% of new colon cancer cases are diagnosed in people who would not be identified as "high risk". Studies of colon cancer cases found that lifestyle factors may put a person at higher risk. These factors include: a diet high in fat and red meat but low in fruits and vegetables, high caloric intake, low levels of physical activity, and obesity. In addition, smoking and excessive alcohol intake may play a role in colon cancer development. Despite avoiding all of these factors, some people will still develop colon cancer. With screening and early detection, these patients can be effectively treated in a majority of the cases.
How Can I Prevent Colon Cancer?
Given the things that put a person at higher risk, a low-fat diet high in fruits and vegetables and low in red meat, together with regular exercise and maintaining a healthy body weight, may aide in prevention. The term chemoprevention can be defined as 'the use of a chemical compound to prevent, inhibit, or reverse the formation of the cancer'. There are ongoing studies looking at vitamins A, E, D, and C, folic acid, calcium, selenium, aspirin, cox-2 inhibitors, statin medications (traditionally used to lower cholesterol) and hormone replacement therapy as potential chemopreventive agents that may prevent or reverse the formation of polyps and colon cancer. Thus far, these studies have been inconclusive, so no specific recommendations can be made for the general population. Some of these agents continue to be evaluated in clinical trials.
What Screening Tests are Available?
Some tumors and polyps may bleed intermittently, and this blood can be detected in stool samples by a test called fecal occult blood testing (FOBT). By itself, FOBT only finds about 24% of cancers. It is recommended by the American Cancer Society that FOBT be done annually, in conjunction with a flexible sigmoidoscopy every 5 years after age 50. This combination of tests detects about 76% of colon tumors. The sigmoidoscope is a slender, flexible tube that has the ability to view about 1/3 of the colon. If a polyp or tumor is detected with this test, the patient must be referred for a full colonoscopy to have the polyp removed and tested for cancer.
The colonoscope is similar to the sigmoidoscope, but is longer and thus can view the entire colon. If a polyp is found, the physician can remove it and send it to a pathology lab to determine if it is adenomatous (cancerous). As a screening method, the American Cancer Society (ACS) recommends that a colonoscopy be done every 10 years after age 50; alternatives include CT colonography (virtual colonoscopy) every 5 years or flexible sigmoidoscopy every 5 years. Patients with a family or personal history should have more frequent screenings; beginning at an earlier age than their relative was when he or she was diagnosed. Patients with a history of inflammatory bowel disease, including ulcerative colitis, are also at increased risk and should have more frequent screening than the general public. No screening modality is perfect. For colonoscopy, the rate of missed lesions is 2-12%.
If a polyp is found on CT colonography, the person would need to have a colonoscopy to biopsy the polyp. The US Preventive Task Force does not recommend CT colonography for general screening. This test is not as good at finding flat polyps, and large flat polyps have a higher risk of developing into colon cancer. Up to 16% of people having their first CT colonography are found to have abnormalities outside the colon that require further testing. In identifying and investigating these abnormalities, there is potential for both benefit and harm. Potential harms arise from additional diagnostic testing and procedures for these lesions found incidentally, which may have no clinical significance. This additional testing also has the potential to burden the patient with additional time off work and costs.
Radiation exposure resulting from CT colonography is reported to be 10 mSv per examination. The harms of radiation at this dose are not certain, but one model predicts that 1 additional individual per 1000 would develop cancer in his or her lifetime at this level of exposure. There is growing research about increased cancer risk due to cumulative radiation exposure from the use of diagnostic and screening tests that involve radiation exposure. On the other hand, improvements in CT colonography technology and practice are lowering this radiation dose.
Patients should talk with their physicians about which screening method is best for them, and how often it should be performed.
Evidence that colonoscopy actually decreases colon cancer deaths is derived from cohort and case control studies (indirect evidence). For example, a study from Ontario, Canada comparing rates of colonoscopy found that for every 1% increase in colonoscopy screening there was a 3% decrease in death from colon cancer. Randomized trials are ongoing.
Despite the effectiveness of screening tests for colon cancer, one study found that only 44% of adults who are age 50 and older had undergone testing. Media focus has helped to raise public awareness of this cancer, but more education is needed.
What are the Signs of Colon Cancer?
Unfortunately, the early stages of colon cancer may not have any symptoms. This is why it is important to have screening tests done even though you may feel well. As the polyp grows into a tumor, it may bleed or obstruct the colon, causing symptoms. These symptoms include:
- Bleeding from the rectum
- Blood in the stool or toilet after a bowel movement
- A change in the shape of the stool (i.e. thinning)
- Cramping pain in the abdomen
- Feeling the need to have a bowel movement when you don't actually have to
As you can see, these symptoms can also be caused by conditions other than cancer. If you experience these symptoms, you should be checked by a doctor.
How is Colon Cancer Diagnosed and Staged?
Once colon cancer is found by the screening tests, further tests are needed to determine the extent of the tumor. The tests used to determine spread of the tumor are CT scans, MRIs, PET/CT scan and lab work. Positron Emission tomography (PET) provides a whole body evaluation and highlight active tumors in the body. Malignant tumors have an increased rate of glycolysis shown by an increase uptake of glucose tracer. PET/CT scan is used to evaluate potential resectable metastasis in the lung and liver. Carcinoembryonic antigen (CEA) level is a marker for colon cancer that is found in the blood and which is elevated in 95% of cases. With these tests, a stage is determined to help dictate the necessary treatment. The TNM staging system assesses the extent of the tumor, nodal involvement, and distant metastases.
After the tumor and lymph nodes are removed by a surgeon, they are examined by a pathologist, who determines how much of the colon wall and lymph nodes have been invaded by tumor. This is reported on your pathology report – you may want to ask for a copy of this report for your personal files.
Using the results from these tests and reports, a stage is determined, which is used to determine the necessary treatment. The TNM staging system assesses the extent of the Tumor, Nodal involvement, and distant Metastases. The stage tells how far the tumor has invaded into the colon wall, and if it has spread to other parts of the body, and is an important piece to deciding on further treatment.
The American Joint Committee on Cancer (AJCC) publishes the TNM staging system for colon cancer, which is as follows:
- Tx- Primary tumor able to be assessed
- Tis- Carcinoma in situ
- T0- No evidence of primary tumor
- T1 - invades submucosa
- T2 - invades muscularis propria
- T3 - invades through muscularis propria into pericolorectal tissues
- T4a - penetrates to the surface of the visceral peritoneum
- T4b - directly invades or is adherent to other organs or structures
- Nx- Lymph nodes not able to be assessed
- N0- No lymph nodes involved with cancer
- N1 - 1 to 3 lymph nodes
- N1a - 1 lymph node
- N1b - 2-3 lymph nodes
- N1c - tumor deposits in the subserosa, mesentery, or nonperitonealized pericolic or perirectal tissues without regional nodal metastasis
- N2 - 4 or more
- N2a - 4-6 lymph nodes
- N2b - 7 or more lymph nodes
- M0 - No evidence for metastatic disease
- M1 - Evidence for distant metastatic disease
- M1a - metastasis confined to one organ or site
- M1b - metastasis in more than one organ/site or the peritoneum
The TNM groupings are combined to give a stage of 0 through IVB. TNM Stage Groupings:
- 0- Tis N0 M0
- I - T1-2 N0 M0
- IIA - T3 N0 M0
- IIB - T4a N0 M0
- IIC - T4b N0 M0
- IIIA - T1-2 N1/1c M0, T1 N2a M0
- IIIB - T3-T4a N1/1c M0, T2-T3 N2a M0, T1-T2 N2b M0
- IIIC - T4a N2a M0, T3-T4a N2b M0, T4b N1-N2 M0
- IVA – Any T Any N M1a
- IVB – Any T Any N M1b
Because the staging system is relatively detailed, a more simplified way of understanding the stage groupings is:
- Stage 0 (also called carcinoma in situ) - the cancer is confined to the outermost portion of the colon wall.
- Stage I - the cancer has spread to the second and third layer of the colon wall, but not to the outer colon wall or beyond. This is also called Dukes' A colon cancer.
- Stage II - the cancer has spread through the colon wall, but has not invaded any lymph nodes (these are small structures that help in fighting infection and disease). This is also called Dukes' B colon cancer.
- Stage III - the cancer has spread through the colon wall and into lymph nodes, but has not spread to other areas of the body. This is also called Dukes' C colon cancer.
- Stage IV - the cancer has spread to other areas of the body (i.e. liver and lungs). This is also called Dukes' D colon cancer.
What are the Treatments for Colon Cancer?
Surgery is the most common treatment for colon cancer. If the cancer is limited to a polyp, the patient can undergo a polypectomy (removal of the polyp), or a local excision, where a small amount of surrounding tissue is also removed. If the tumor invades the bowel wall or surrounding tissues, the patient will require a partial resection (removal of the cancer and a portion of the bowel) and removal of local lymph nodes to determine if the cancer has spread into them. After the tumor is removed, the two ends of the remaining colon are reconnected, allowing normal bowel function. In some situations, it may not be possible to reconnect the colon, and a colostomy (an opening in the abdominal wall to allow passage of stool) is needed, which may be temporary or permanent.
Despite the fact that a majority of patients have the entire tumor removed by surgery, as many as 50 to 60% will develop a recurrence without further treatment. Chemotherapy is given to reduce this chance of recurrence, particularly when initiated within 4 week of surgery. There is some controversy over whether or not patients with stage II disease should receive chemotherapy. Studies have not consistently shown a benefit in treating these patients or have shown only a very small benefit. Many patients with stage II disease are followed closely, but receive no chemotherapy. Generally, patients with stage II disease who present with a bowel perforation or obstruction, or who have large or poorly differentiated tumors (determined by a pathologist looking at the tumor under a microscope), are considered at higher risk for recurrence and are treated with 6 months of fluorouracil (5-FU), leucovorin (LV), with or without oxaliplatin chemotherapy. Work is being done to further clarify who among the stage II group is high risk, which will be helpful to providers making treatment decisions. There are assays available to assess molecular and genetic markers in stage II patients, which can be helpful in treatment decisions.
Patients who present with stage III colon cancer are treated with a regimen of chemotherapy, including some combination of fluorouracil (5-FU), leucovorin, and oxaliplatin for 6 months, resulting in improved survival rates when compared with surgery alone. The addition of other agents, including irinotecan and bevacizumab, in combination with 5-FU/LV has not been shown to benefit stage III patients. After completion of this therapy, they are monitored for recurrence of the disease. Capecitabine (Xeloda) is an oral form of fluorouracil, that is used frequently as a replacement for intravenous 5-FU.
Forty to fifty percent of patients have metastatic disease (cancer that has spread to other organs, also called stage IV) at the time of diagnosis, or have a recurrence of the disease after therapy. Unfortunately, with the exception of selected patients who have limited liver/lung metastases, stage IV disease is not considered cureable. Nevertheless, patients can have improved quality of life and longer survival with chemotherapy treatment. The standard therapy for patients with advanced disease is some combination of fluorouracil, leucovorin, irinotecan (CPT-11 or Camptosar), oxaliplatin (Eloxitin), bevacizumab (Avastin), cetuximab (Erbitux), and capecitabine. Regimens adding either irinotecan or oxaliplatin to fluorouracil and leucovorin were found to be more effective than using the fluorouracil and leucovorin alone.
Targeted therapies are drug treatments that target a specific abnormality found in the cancer cells. The following are targeted therapies that are commonly used in the treatment of colon cancer.
Bevacizumab (Avastin) is a type of treatment called anti-angiogenic therapy. Tumors need nutrients to survive and are able to get these nutrients by growing new blood vessels. This medication works by attacking the new blood vessels the tumor has formed -- in other words, by cutting off its food source. Bevacizumab is used in combination with chemotherapy for patients with metastatic disease.
Epidermal growth factor receptor (EGFR) is abnormally over expressed in many cancers (including those of the colon and rectum), so inhibition of EGFR can result in a decrease in tumor cell growth and decreased production of other factors responsible for metastasis (tumor spread). Panitumumab and cetuximab are monoclonal antibodies that exert cancer fighting properties by competitively inhibiting the binding of epidermal growth factor to EGFR, which prevents epidermal growth factor from working, and hence not allowing cancer growth to occur. These agents are generally used for patients who tumor type is deemed “KRAS wild-type”. This means that there is no mutation with the KRAS protein.
Treatment recommendations for patients with metastatic disease depend on whether the patient is appropriate for intensive therapy. Chemotherapy options for patients with metastatic disease depend on what treatment they initially received. Clinical trial participation may be recommended before standard therapy.
Colon cancer is not typically treated with radiation therapy. If the cancer has invaded another organ, or attached itself to the abdominal wall, radiation therapy may be a treatment option. One reason for the limited role of radiation is that it is a local treatment typically aimed at a "target." Once the colon cancer has been surgically resected, the "target" or high-risk area for disease recurrence is not very easy to define. Furthermore, if the cancer has spread to other organs, chemotherapy (rather than radiation therapy) is able to reach distant areas of spread of tumor cells.
Interventional radiologists are specialists who use radiology techniques, such as CT scan, to access areas of the body and treat diseases without traditional surgery. These techniques are sometimes called "minimally invasive". In some cases, these physicians are able to help patients with colon cancer that has metastasized to the liver or lung. The techniques currently being used by these specialists include: CT directed biopsies, chemoembolization, radiofrequency ablation and radioembolization. By entering a patient's blood vessels, the physician can thread a catheter all the way to the liver and give treatment directly to the tumor.
Radiofrequency ablation (RFA) is a local treatment that kills the tumor cells with heat, while sparing healthy liver tissue. When the tumor is too large or in a location not amenable to RFA, embolization may be used to cut off the blood supply to the tumor, deliver radiation to a tumor (called radioembolization), or combine this technique with chemotherapy to deliver the cancer drug directly to the tumor (called chemoembolization). These therapies are not considered curative, but can provide improved quality of life and extend survival.
Some patients may benefit from having an infusion pump inserted to infuse chemotherapy directly into the liver. IR physicians can also perform palliative procedures, such as inserting a stent to relieve an obstruction, treating certain types of pain, inserting central catheters or treating blood clots.
Once a patient has completed chemotherapy, they must be followed closely for recurrence. The guidelines for follow-up surveillance, written by the National Comprehensive Cancer Network (NCCN) are: physical exam (including digital rectal exam) every 3 months for 2 years, then every 6 months for 3 years; CEA level (if elevated preoperatively) checked every 3 months for 2 years, then every 6 months for 3 years; and colonoscopy in 1 year, with a repeat in 1 year if abnormal, or every 2-3 years if no polyps are found. Patients who are at high risk of developing colon cancer recurrence, a yearly CT scan is recommended.
Clinical trials have played and continue to play an important role in the treatment of colon cancer. In the past 20 years, considerable improvements have been made in colon cancer therapy, with overall survival rates increasing from 45 to 75 percent. The treatments we have today were refined through clinical trials, and many new avenues continue to be explored. Talk with your physician about current clinical trials for colon cancer in your area or use the OncoLink Clinical Trials Matching Service.
After treatment, talk with your oncology team about receiving a survivorship care plan, which can help you manage the transition to survivorship and learn about long-term concerns and life after cancer. You can create a survivorship care plan on OncoLink.
This article is meant to give you a better understanding of colon cancer. Use this knowledge when meeting with your physician, making treatment decisions, and continuing your search for information.
Colon Cancer Alliance - The Colon Cancer Alliance brings the voice of survivors to battle colorectal cancer through patient support, education, research and advocacy.
Fight Colorectal Cancer - Provides advocacy, education and support.
Chris 4 Life Colon Cancer Foundation - Provides education, support and funds research.
The Colon Club - Promotes education and awareness in interesting and out of the box ways.
American Society of Colon and Rectal Surgeons - Society for colon and rectal surgeons and other surgeons dedicated to the treatment of patients with diseases and disorders affecting the colon, rectum and anus.
Colon-Rectal.com - Physicians with decades of experience and specialized training in caring for these types of problems have contributed text and images to this website.
Abeloff, M., Armitage, J., Niederhuber, J., Kastan, M. & McKenna, G. (Eds.): Clinical Oncology (2004). Elsevier, Philadelphia, PA.
The American Cancer Society. Facts and Figures 2015. www.cancer.org
Baxter NN, Goldwasser MA, Paszat LF, Saskin R, Urbach DR, Rabeneck L. Association of colonoscopy and death from colorectal cancer. Ann Intern Med. 2009;150:1-8.
Benson, Al New Approaches to the Adjuvant Therapy of Colon Cancer. The Oncologist. 2006; 11(9): 973-980.
Biagi JJ, Raphael M, King WD, et al. The impact of time to adjuvant chemotherapy (AC) on survival in colorectal cancer (CRC): A systematic review and meta-analysis. Abstract #364. ASCO 2011 Gastrointestinal Cancers Symposium. San Francisco, CA.
Blumberg, D. & Ramanathan, R. K. (Treatment of Colon and Rectal Cancer. Journal of Clinical Gastroenterology. 2002; 34(1): 15-26.
Brown, DB et al. Society of Interventional Radiology Position Statement on Chemoembolization of Hepatic Malignancies. J Vasc Interv Rad. 2006; 17 (2): 217-223.
DeGramont A, Van Cutsem E, Taberno J, et al. AVANT: Results from a randomized, three-arm multinational phase III study to investigate bevacizumab with either XELOX or FOLFOX4 versus FOLFOX4 alone as adjuvant treatment for colon cancer. Abstract#362. ASCO 2011 Gastrointestinal Cancers Symposium. San Francisco, CA.
Haller, D, Cassidy J, Tabernero, J, et al. First efficacy findings from a randomized phase III trial of capecitabine + oxaliplatin vs. bolus 5-FU/LV for stage III colon cancer (NO16968): No impact of age on disease-free survival (DFS). Abstract#284. ASCO 2010 Gastrointestinal Cancers Symposium. Orlando, FL.
Lieberman, D. A. & Weiss, D. G. (2001) One-Time Screening for Colorectal Cancer with Combined Fecal Occult Blood Testing and Examination of the Distal Colon. New Eng J Med 2001;345(8): 555-560.
National Cancer Institute. General Information About Colon Cancer.
NCCN Clinical Practice Guidelines: Colon Cancer (V.2.2015).
Pickhardt, PJ. "Colorectal Cancer Screening: Virtual Colonscopy vs Conventional Colonscopy: Virtual Colonscopy" Oral Presentation. ASCO 2011 Gastrointestinal Cancers Symposium. Jan 22, 2011. San Francisco, CA.
Rosenberg R, Maak M, Simon I, et al. Independent validation of a prognostic genomic profile (ColoPrint) for stage II colon cancer (CC) patients. Abstract #358. ASCO 2011 Gastrointestinal Cancers Symposium. San Francisco, CA.
Siegel, R.L, Miller, K. D. & Jemal, A. (2015). Cancer Statistics, 2015. CA: A Cancer Journal for Clinicians, 65(1). 5-29.
Society of Interventional Radiology: Patient information.
Van Cutsem E, Labianca R, Bodoky G, et al: Randomized phase III trial comparing biweekly infusional fluorouracil/leucovorin alone or with irinotecan in the adjuvant treatment of stage III colon cancer: PETACC-3. J Clin Oncol. 2009; 27: 3117.
Wilkes, G.M. (2011). Colon, Rectal & Anal Cancer. In Yarbro C.H, Wujcik, D. & Gobel, B.H. (Eds.). Cancer Nursing (pp. 1205-1237). Sudbury, MA: Jones and Bartlett.
Ychou M, Raoul JL, Douillard JY, et al: A phase III randomised trial of LV5FU2 + irinotecan versus LV5FU2 alone in adjuvant high-risk colon cancer (FNCLCC Accord02/FFCD9802). Ann Onc 2009; 20:674.
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