The survival rate for a carcinoid tumor depends on the stage of the tumor at the time of its diagnosis. Overall, the survival rates for carcinoid tumors have been observed to be good. Because they are often found at an earlier stage, it is easier to treat them.
The survival rate is analyzed in a large study, in which the lifespan of a large population, after the diagnosis of cancer, is observed for a specific timeframe. It is generally presented as a five-year survival rate—what percentage of people lived for at least five years after the diagnosis.
For example, the five-year survival rate (as shown in Table 1) for tumor limited only to the specific organ (localized tumor) is 97%. This means that 97 of 100 people who were diagnosed with carcinoid tumors could live for at least five years or more.
|*SEER Stage||Five-Year Relative Survival Rate|
|All SEER stages combined||94%|
*SEER Stage: Stage of the tumor as determined by the Surveillance, and End Results (SEER) Program of the National Cancer Institute (NCI); Digestive system: the stomach, small intestine, colon, appendix, cecum, and rectum; Reginal: Tumor that has spread to the adjacent lymph nodes; Distant: Tumor that has spread to the distant organs.
Carcinoid tumors of the lung generally have better survival outcomes than other forms of lung cancers. They have an overall 5-year survival rate of 78-95% and a 10-year survival rate of 77-90%.
Life expectancy is not good for the carcinoid tumor that has spread to other organs of the body.
What is a carcinoid tumor?
A carcinoid tumor is a rare cancer of the neuroendocrine system (a system of the nerve cells that also produces hormones in the body). It is usually a slow-growing tumor.
The tumor grows in the following organs:
“Carcinoid syndrome” is the advanced form of the carcinoid tumor. It is a term given for a set of symptoms that develop when the carcinoid tumor spreads to other organs and releases hormones such as serotonin that lead to hormonal imbalance.
What are the signs and symptoms of a carcinoid tumor?
The signs and symptoms produced by the tumor depend upon the organ on which the tumor has developed. As they are fair general, they can be easily mistaken for illnesses other than the tumor. Hence, the doctor will take your complete medical history and order various tests before diagnosing the carcinoid tumor.
It is also possible that you may have a carcinoid tumor with no signs and symptoms. For example, in a carcinoid tumor of the appendix, the doctor might discover it during surgery a such as removal of the appendix.
|Location of the carcinoid tumor||Signs and symptoms|
Abdominal pain, diarrhea, constipation, and bleeding from the rectum
Cough, blood in the cough, breathlessness, chest pain, and fatigue
Stomach pain, weight loss, tiredness, and weakness
What causes carcinoid tumors?
Doctors do not know the exact cause of carcinoid tumors. However, they have found out some factors that may increase your chances of developing one. These include:
- Having a close family member with a carcinoid tumor
- Multiple endocrine neoplasia type 1 (MEN1)
- Having parents with any of the following cancers:
- Neurofibromatosis (a genetic disorder that causes tumors to form on the nerve tissue)
- Tuberous sclerosis (a rare, multisystem genetic disease that causes tumors or growths in organs)
Can second cancers develop after carcinoid tumor treatment?
Unfortunately, you may develop other cancers (known as secondary cancers) unrelated to the carcinoid tumor even after you get treated for the carcinoid tumor.
As a survivor of a lung carcinoid tumor, you have a higher risk of
A carcinoid tumor of the digestive system puts you at a higher risk of
Can you lower your risk of second cancer?
A step like quitting tobacco certainly helps in lowering the risk of secondary cancer after treatment for a carcinoid tumor. This is true not only for lung carcinoid tumors specifically but also for carcinoid tumors in other organs.
To help maintain good health, you, as a carcinoid survivor, need to
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Carcinoid Lung Tumors. Available at: https://emedicine.medscape.com/article/426400-overview#a2
Carcinoid Tumor. Available at: https://emedicine.medscape.com/article/986050-overview