Colorectal cancer natural history: Difference between revisions
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*The progression from an [[adenomatous]] polyp to colorectal cancer may take 10-15 years<ref name="pmid10089106">{{cite journal| author=Winawer SJ| title=Natural history of colorectal cancer. | journal=Am J Med | year= 1999 | volume= 106 | issue= 1A | pages= 3S-6S; discussion 50S-51S | pmid=10089106 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10089106 }} </ref> | *The progression from an [[adenomatous]] polyp to colorectal cancer may take 10-15 years<ref name="pmid10089106">{{cite journal| author=Winawer SJ| title=Natural history of colorectal cancer. | journal=Am J Med | year= 1999 | volume= 106 | issue= 1A | pages= 3S-6S; discussion 50S-51S | pmid=10089106 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10089106 }} </ref> | ||
*It is a multistep process that involves genetics, abnormalities of cell regulation, and environmental triggers | *It is a multistep process that involves genetics, abnormalities of cell regulation, and environmental triggers | ||
*The patient may present with | *The patient may present with the following: | ||
:*Change in bowel habits such as change in frequency, change in the quality of stools, change in consistency of stools | :*Change in bowel habits such as change in frequency, change in the quality of stools, change in consistency of stools | ||
:*[[Intestinal obstruction]] | :*[[Intestinal obstruction]] | ||
:*Intestinal [[perforation]] | :*Intestinal [[perforation]] | ||
:*Hematochezia or bleeding per rectum | :*[[Hematochezia]] or bleeding per rectum | ||
:*Mucus in stools | :*Mucus in stools | ||
:*Abdominal cramps or discomfort | :*Abdominal cramps or discomfort | ||
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:*Nausea/vomiting | :*Nausea/vomiting | ||
:*Unexplained weight loss | :*Unexplained weight loss | ||
:*Unexplained loss of appetite | :*Unexplained loss of [[appetite]] | ||
:*[[Weakness]] | :*[[Weakness]] | ||
:*[[Fatigue]] | :*[[Fatigue]] | ||
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:*Lungs - dyspnea, cough with blood-stained sputum, persistent pain or discomfort in the chest | :*Lungs - dyspnea, cough with blood-stained sputum, persistent pain or discomfort in the chest | ||
:*Liver - abdominal pain, swelling in hands/feet, [[itchiness]], [[jaundice]], dark-colored urine | :*Liver - abdominal pain, swelling in hands/feet, [[itchiness]], [[jaundice]], dark-colored urine | ||
:*Bones - pain, fractures | :*Bones - pain, [[fractures]] | ||
:*Brain/spinal cord - pain, confusion, memory loss, headache, blurred or double vision, difficulty with speech, difficulty with movement or [[seizures]] | :*Brain/spinal cord - pain, [[confusion]], memory loss, [[headache]], blurred or double vision, difficulty with speech, difficulty with movement or [[seizures]] | ||
*Once the cancer spreads to the other organs, it is most likely fatal | *Once the cancer spreads to the other organs, it is most likely fatal | ||
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*[[Fistula]] formation | *[[Fistula]] formation | ||
*Gastrointestinal bleeding | *Gastrointestinal bleeding | ||
*[[Metastasis]] - usually | *[[Metastasis]] - usually in the liver and lungs but may occur in other sites | ||
*Cancer recurrence - local (site of the original tumor), regional (in the lymph nodes near the primary tumor) or distal (in another part of the body) | *Cancer recurrence - local (site of the original tumor), regional (in the lymph nodes near the primary tumor) or distal (in another part of the body) | ||
*Common [[radiation therapy]] adverse effects - skin discoloration, skin burns, [[headache]], [[fatigue]], [[hair loss]], [[nausea]], [[vomiting]], and/or [[confusion]] | *Common [[radiation therapy]] adverse effects - skin discoloration, skin burns, [[headache]], [[fatigue]], [[hair loss]], [[nausea]], [[vomiting]], and/or [[confusion]] | ||
*Common [[chemotherapy]] adverse effects - [[hair loss]], [[fatigue]], [[weakness]], [[nausea]], [[vomiting]], risk of [[infection]], and/or [[diarrhea]] | *Common [[chemotherapy]] adverse effects - [[hair loss]], [[fatigue]], [[weakness]], [[nausea]], [[vomiting]], risk of [[infection]], and/or [[diarrhea]] | ||
*Common post-surgical complications - colon leakage, organ damage, hematoma, bleeding, infection | *Common post-surgical complications - colon leakage, organ damage, [[hematoma]], [[bleeding]], [[infection]] | ||
*Metachronous colon cancer (development of a second primary cancer) - develops six or more months after the primary tumor and is often in another site | *Metachronous colon cancer (development of a second primary cancer) - develops six or more months after the primary tumor and is often in another site | ||
*Death | *Death | ||
==Prognosis== | ==Prognosis== | ||
Survival is directly related to the detection and the type of cancer involved. Survival rates for early stage detection is | Survival is directly related to the detection and the type of cancer involved. Survival rates for early stage detection is approximately 5 times that of late stage cancers. | ||
The 5 year survival rates depending upon the stage of colorectal cancer are as follows: | The 5 year survival rates depending upon the stage of colorectal cancer are as follows: | ||
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CEA level may also be directly related to the prognosis of disease, since its concentration correlates with the bulk of tumor tissue. | CEA level may also be directly related to the prognosis of disease, since its concentration correlates with the bulk of tumor tissue. | ||
'''Poor prognostic factors of patients with | '''Poor prognostic factors of patients with hepatic metastasis include the following:''' | ||
*[[Synchronous]] (diagnosed simultaneously) liver and primary colorectal tumors | *[[Synchronous]] (diagnosed simultaneously) liver and primary colorectal tumors | ||
*A short time between detecting the primary cancer and subsequent development of liver metastasis | *A short time between detecting the primary cancer and subsequent development of liver metastasis |
Revision as of 18:50, 16 July 2015
Colorectal cancer Microchapters |
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Treatment |
Case Studies |
Colorectal cancer natural history On the Web |
American Roentgen Ray Society Images of Colorectal cancer natural history |
Risk calculators and risk factors for Colorectal cancer natural history |
To view the natural history of familial adenomatous polyposis (FAP), click here
To view the natural history 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.; Elliot B. Tapper, M.D.
Overview
The progression from an edematous polyp to colorectal cancer may take 10-15 years. Complications may arise if the cancer is not eradicated or from the treatment itself. Complications include intestinal obstruction, gastrointestinal bleeding, metastasis, cancer recurrence, radiation therapy adverse effects, chemotherapy adverse effects, post-surgical complications, metachronous colon cancer, and death. The 5 year survival rates depend upon the stage of colorectal cancer.
Natural history
- The progression from an adenomatous polyp to colorectal cancer may take 10-15 years[1]
- It is a multistep process that involves genetics, abnormalities of cell regulation, and environmental triggers
- The patient may present with the following:
- Change in bowel habits such as change in frequency, change in the quality of stools, change in consistency of stools
- Intestinal obstruction
- Intestinal perforation
- Hematochezia or bleeding per rectum
- Mucus in stools
- Abdominal cramps or discomfort
- Tenesmus
- Diminished caliber of stools
- Rectal pain (usually associated with rectal cancer)
- Nausea/vomiting
- Unexplained weight loss
- Unexplained loss of appetite
- Weakness
- Fatigue
- Dizziness
- Palpitations
- If the cancer spreads to other organs, the following symptoms may develop:
- Lungs - dyspnea, cough with blood-stained sputum, persistent pain or discomfort in the chest
- Liver - abdominal pain, swelling in hands/feet, itchiness, jaundice, dark-colored urine
- Bones - pain, fractures
- Brain/spinal cord - pain, confusion, memory loss, headache, blurred or double vision, difficulty with speech, difficulty with movement or seizures
- Once the cancer spreads to the other organs, it is most likely fatal
Complications
Complications of colorectal cancer include[2]:
- Intestinal obstruction
- Intestinal perforation
- Fistula formation
- Gastrointestinal bleeding
- Metastasis - usually in the liver and lungs but may occur in other sites
- Cancer recurrence - local (site of the original tumor), regional (in the lymph nodes near the primary tumor) or distal (in another part of the body)
- Common radiation therapy adverse effects - skin discoloration, skin burns, headache, fatigue, hair loss, nausea, vomiting, and/or confusion
- Common chemotherapy adverse effects - hair loss, fatigue, weakness, nausea, vomiting, risk of infection, and/or diarrhea
- Common post-surgical complications - colon leakage, organ damage, hematoma, bleeding, infection
- Metachronous colon cancer (development of a second primary cancer) - develops six or more months after the primary tumor and is often in another site
- Death
Prognosis
Survival is directly related to the detection and the type of cancer involved. Survival rates for early stage detection is approximately 5 times that of late stage cancers.
The 5 year survival rates depending upon the stage of colorectal cancer are as follows:
The numbers below come from the National Cancer Institute's SEER database, looking at people diagnosed with colon cancer between 2004 and 2010.
Stage | 5-year Relative Survival Rate |
I | 92% |
IIA | 87% |
IIB | 63% |
IIIA | 89% |
IIIB | 69% |
IIIC | 53% |
IV | 11% |
The numbers below come from the National Cancer Institute's SEER database, looking at people diagnosed with rectal cancer between 2004 and 2010.
Stage | 5-year Relative Survival Rate |
I | 87% |
IIA | 80% |
IIB | 49% |
IIIA | 84% |
IIIB | 71% |
IIIC | 58% |
IV | 12% |
CEA level may also be directly related to the prognosis of disease, since its concentration correlates with the bulk of tumor tissue.
Poor prognostic factors of patients with hepatic metastasis include the following:
- Synchronous (diagnosed simultaneously) liver and primary colorectal tumors
- A short time between detecting the primary cancer and subsequent development of liver metastasis
- Multiple metastatic lesions
- Large-sized metastatic lesions, which can be measured by a high concentration of carcino-embryonic antigen (CEA)
References
- ↑ 1.0 1.1 Winawer SJ (1999). "Natural history of colorectal cancer". Am J Med. 106 (1A): 3S–6S, discussion 50S-51S. PMID 10089106.
- ↑ Tebbutt, N C (2003). "Intestinal complications after chemotherapy for patients with unresected primary colorectal cancer and synchronous metastases". Gut. 52 (4): 568–573. doi:10.1136/gut.52.4.568. ISSN 0017-5749.