Rectal Cancer: The Basics

Carolyn Vachani, MSN, RN, AOCN
Updated by: Lara Bonner Millar, MD
The Abramson Cancer Center of the University of Pennsylvania
Last Modified: February 18, 2011

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What is the rectum?

The rectum is located at the end of the colon and is about 5 inches in length. The rectum is normally empty, except when stool is propelled by the upper colon into the rectum just prior to a bowel movement. At that time, stool is ready to be excreted through the anal canal. The anal canal has two muscular "valves", called the internal and external sphincters, through which the stool must pass. The sphincters allow us to retain stool until we are ready to have a bowel movement, at which time the sphincters relax, releasing the stool.

What is rectal cancer?

Rectal cancer is malignant (or cancerous) tissue that grows in the wall of the rectum. The majority of tumors begin when normal tissue in the rectum wall forms an adenomatous polyp, or pre-cancerous growth, projecting from the rectal wall lining. 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 rectal cancer?

In 2008, there will be an estimated 40,740 new cases of rectal cancer in the United States (23,490 in men and 17,250 in women). In general, colon and rectal cancers are grouped together and have the same risk factors associated with them. The average age of diagnosis is 66 years of age, and risk increases with age. Individuals with a personal or family history of colorectal cancer or polyps, inherited colorectal cancer syndromes (i.e., FAP and HNPCC, and patients with ulcerative colitis or Crohn's disease are at higher risk, and thus 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. About 80% of new colorectal cancer cases are diagnosed in people who would not be identified as "high risk". Studies of colorectal 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 colorectal cancer development.

Despite avoiding all of these factors, some people will still develop colon or rectal cancer. With screening and early detection, these patients can be cured in a majority of the cases.

How can I prevent rectal 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, regular exercise, and maintaining a healthy body weight may all aid 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, and hormone replacement therapy as potential chemopreventive agents that may prevent or reverse the formation of polyps and colorectal cancer. Thus far, these studies have been inconclusive, and thus no specific recommendations have been made for the general population. Some of these agents continue to be evaluated in clinical trials. Recently, an interesting case-control study of 1,800 Israeli women found that women taking bisphosphonates (medication for osteoporosis) for a year or more had about a 50% reduction in the diagnosis of colorectal cancer compared to women not taking the drug. This reduction has not yet been “proven” by a randomized clinical trial, but many in the oncology community are calling for more studies on the use of bisphosphonates as chemoprevention.

What screening tests are available?

The one screening test that is specific to rectal cancer is a digital rectal exam (DRE). This test consists of a physician inserting a gloved finger into the patient's rectum and feeling for abnormal growths or strictures. Studies have not proven that screening with DRE actually decreases deaths due to rectal cancer. Other screening tests are the same as those used for colon cancer screening, including fecal occult blood testing, colonoscopy, and sigmoidoscopy. These tests screen both the colon and the rectum.

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 colorectal tumors. The sigmoidoscope is a slender, flexible tube that has the ability to view the rectum and the lowest part of the colon. If a polyp or tumor is detected with this test, the patient must be referred for a full colonoscopy.

The colonoscope is similar to the sigmoidoscope, but is longer and can view the entire rectum and 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 recommends that a colonoscopy be done every 10 years after age 50. Patients with a family or personal history should have more frequent screenings; these should begin at an age that is ten years younger than their relative was at diagnosis. Patients with a history of ulcerative colitis are also at increased risk and should have more frequent screening than the general public. Patients should talk with their physicians about which screening method is best for them, and how often it should be performed. You can learn more about screening by reading Basic Information about Colorectal Cancer and Colorectal Cancer Screening.

What are the signs of rectal cancer?

Unlike colon cancers, most rectal cancers cause symptoms. These include: red blood seen in the stool, unexplained constipation alternating with diarrhea, changes in the diameter of stool (patients may notice "pencil-thin stools"), and tenesmus, which is a sensation of needing to have a bowel movement when you don ' t and/or being unable to empty the rectum. If tumors have become more advanced, they can invade the nearby tissues and cause bladder incontinence or pain due to pressure in the buttocks or perineum.

How is rectal cancer diagnosed and staged?

Once rectal 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, and endoscopic ultrasound (EUS). The EUS is a type of ultrasound that uses sound waves to determine the depth of the tumor and whether or not surrounding lymph nodes are involved. A biopsy is typically done during an EUS, colonoscopy or proctoscopy (a test which allows the doctor to view only the rectal area) to verify the type of tumor. Carcinoembryonic antigen (CEA) level is a marker for colon cancer that is found in the blood and which is elevated in 95% of cases. Women with advanced tumors should also have a pelvic exam to assess if the tumor has invaded into the vagina or cervix. 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.

Primary Tumor:

  • T1 - invades submucosa
  • T2 - invades muscularis propria
  • T3 - invades through muscularis propria into pericolorectal tissues
  • T4
    • T4a - penetrates to the surface of the visceral peritoneum
    • T4b - directly invades or is adherent to other organs or structures

Lymph Nodes:

  • 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

Distant Metastasis:

  • M0 - none
  • M1 - yes
    • M1a - metastasis confined to one organ or site
    • M1b - metastasis in more than one organ/site or the peritoneum

Stage Grouping:

  • I - T1-2 N0 M0
  • IIA - T3 N0 M0
  • IIB - T4a N0 M0
  • IIC - T4b N0 M0
  • IIIA - T1-2 N1 M0, T1 N2a M0
  • IIIB - T3-T4a N1 M0, T2-T3 N2a, T1-T2 N2b
  • IIIC - T4a N2a, T3-T4a N2b, T4b N1-N2
  • IVA - M1a
  • IVB - M1b

Because the staging system is relatively detailed, a more simplified way of understanding the stage groupings is:

  • Stage 0: the tumor is confined to the first layer of the rectal tissue. It is also called carcinoma in situ
  • Stage I: the tumor has spread through the innermost lining of the rectum into the second and third layers of the inside wall of the rectum, but has not spread outside the rectum
  • Stage II: the tumor has spread through the rectal wall into surrounding tissue, but has not spread to the lymph nodes
  • Stage III: the tumor has spread to the surrounding lymph nodes, but has not spread to other areas of the body
  • Stage IV: the tumor has spread to other areas of the body, such as the liver and lungs

There are other staging systems used in clinical practice, but this one is the most commonly used. See Understanding Your Pathology Report for more information.

What are the treatments for rectal cancer?

Surgery

Over the past twenty years, there have been significant improvements in surgical techniques for the treatment of rectal cancer. In the past, a majority of patients required a colostomy after rectal cancer surgery and developed significant side effects (such as incontinence and male impotence) from nerve damage that frequently occurred during the surgery. The utilization of pre-operative chemoradiation (combination of chemotherapy and radiation) and improved surgical techniques has led to fewer side effects and fewer patients requiring colostomy.

Surgery is the most common treatment for rectal cancers. If the tumor is relatively small, it can be removed by a surgical procedure called local excision, which removes only the cancerous area.

A larger tumor requires a resection (removal of the tumor and some healthy tissue surrounding it) and anastomosis (the two tumor-free ends of the bowel are reconnected). If the bowel ends cannot be reconnected, a colostomy is made. Preoperative chemotherapy & radiation (called neoadjuvant therapy) can improve how successful the surgeon is at completely removing the tumor.

The most commonly performed surgical procedure today is the total mesorectal excision or TME. This procedure removes the rectum and the mesorectum, an area of fatty tissue below the rectum that contains lymph nodes, which are the most common area for the cancer to spread. In the hands of an experienced surgeon, the number of patients requiring colostomy with this procedure is low. TME, along with neoadjuvant chemoradiation, has led to decreases in recurrences in the rectal area from 40% to less than 10% and has improved overall survival from 50 to 75% in the last 40 years.

Diagram of TME excision

Rectal Cancer The Basics

In addition, surgeons used to perform the resection through the abdomen (called abdomino-perineal resection or APR). Today, the TME is most often performed with a low anterior resection (LAR), which

In some cases, even though the surgeon is able to remove all of the visible tumor, a person may also be recommended chemotherapy and/or radiation therapy to prevent the cancer from coming back (also called recurrence). These recommendations are based on what the pathologist finds when examining the tumor under a microscope, including if the margins of the specimen are free of tumor, the tumor size, and if any blood vessels or lymph nodes are involved.

The normal rectum acts as a holding area for stool. When an ultra low rectal resection and anastomosis are needed, the holding area is lost, leading to more frequent bowel movements and/or incontinence. To alleviate this problem, the colonic J-pouch was developed. This procedure uses the remaining bowel to create a J-shaped pouch, which then acts as a new holding area for the stool. It is usually about 5-6 cm in length and significantly reduces the number of bowel movements and incontinence.

Radiation and Chemotherapy

Patients with stage 0 and I disease are typically treated with surgery only. Patients with stage II and III disease are at a high risk of recurrence and should be treated with chemotherapy and radiation either pre-operatively (called neoadjuvant therapy) alone or in conjunction with post-operative therapy (called adjuvant therapy).

Due to the large size of the pelvis (the bony structure in which the rectum lies), it is often difficult for a surgeon to remove enough normal surrounding tissue to obtain adequate tumor-free margins. This is especially true for larger tumors. Giving chemoradiation pre-operatively can shrink a tumor that would not have been surgically removable initially, therefore making these patients candidates for potentially curative surgery. This is known as "downstaging" the tumor. Downstaging with chemoradiation has also allowed patients with tumors that would otherwise require a colostomy to now have a resection and anastomosis following treatment. Studies have shown that giving fluorouracil (5-FU) in combination with radiation therapy (called chemoradiation) before surgery (called neoadjuvant therapy) results in less short and long term toxicity and fewer recurrences of the tumor in the rectal area, when compared to giving the therapy after surgery. Because of this, neoadjuvant therapy has become the standard of care for rectal cancer.

Patients with stage IV rectal cancer may be offered resection of the tumor, radiation and/or chemotherapy. Some patients may be candidates for surgical management of cancer that has spread to other nearby organs (i.e. liver, ovaries). Most of these treatments are to alleviate symptoms, but are not considered curable.

Therapy for patients with advanced disease includes a combination of fluorouracil, leucovorin, and irinotecan (CPT-11 or Camptosar) or oxaliplatin (Eloxitin). Regimens incorporating irinotecan or oxaliplatin were found to be more effective than fluorouracil and leucovorin alone in these patients.

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.

Cetuximab (Erbitux) and panitumumab (Vectibix) are types of monoclonal antibodies that target cancer cells specifically, sparing the normal cells and therefore causing fewer side effects. Cetuximab causes the patient's immune system to recognize the cancer cells as foreign and attack them and is given either alone or in conjunction with chemotherapy agents.

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 exerts its 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.

Capecitabine (Xeloda), an oral form of fluorouracil, is also being used in the treatment of rectal cancers when the patient cannot tolerate the above therapies or has progressed on these therapies.

Follow-up care

Once a patient has completed chemotherapy, he or she must be followed closely for recurrence. The guidelines for follow-up surveillance, written by the National Comprehensive Cancer Network, are: physical exam (including digital rectal exam) every 3 months for 2 years, then every 6 months for 3 years; CEA level checked (if elevated at diagnosis) 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. There is not enough evidence to support or refute the use of chest x-ray or CT scan for surveillance at this time, so this varies from physician to physician and is more likely used in higher risk cases.

Clinical trials have played and continue to play an important role in the treatment of colorectal cancer. In the past 20 years, considerable improvements have been made in colorectal 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 rectal cancer available in your area.

This article is meant to give you a better understanding of rectal cancer. Use this knowledge when meeting with your physician, making treatment decisions, and continuing your search for information.

You can also learn more about colorectal cancer on OncoLink through the related links on the left.

References

  • Abeloff, M., Armitage, J., Niederhuber, J., Kastan, M. & McKenna, G. (Eds.): Clinical Oncology (2004). Elsevier, Philadelphia, PA.
  • The American Cancer Society. Facts and Figures 2005. www.cancer.org
  • Blumberg, D. & Ramanathan, R. K. (2002) Treatment of Colon and Rectal Cancer. Journal of Clinical Gastroenterology, 34(1), 15-26.
  • DeVita, V., Hellman, S., & Rosenberg, S. Cancer: Principles and Practice of Oncology, Seventh Edition (2005). Lippincott, Williams & Wilkins, Philadelphia, Pennsylvania.
  • 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. The New England Journal of Medicine, 345(8), 555-560.
  • National Cancer Institute. General Information About Rectal Cancer.
  • National Comprehensive Cancer Network Practice Guidelines for Colorectal Cancer (2005). www.nccn.org
  • Rennert G, Pinchev M. Rennert HS, et al. Association of bisphosphonate use and risk of colorectal cancer J Clin Oncol 2011; 29 (suppl 4; abstr 371)