Kaposi sarcoma (KS) is a rare cancer that starts in cells that line the lymph or blood vessels. It differs from other sarcomas because it can appear in several parts of the body at the same time.
KS usually develops on or under the skin. It may also happen in lymph nodes or in the layers of tissue that line the mouth, nose, throat or anus. KS can also develop in the lungs or parts of the
Risk factors @(Model.HeadingTag)>
These are the main risk factors for KS:
- infection with human herpesvirus 8, or HHV-8 (also called Kaposi sarcoma-associated herpesvirus, or KSHV) – a virus found in the tumours of people with AIDS-related KS
- having a weakened immune system (immunosuppression)
Types of Kaposi sarcoma @(Model.HeadingTag)>
There are 4 main types of KS.
Classic Kaposi sarcoma @(Model.HeadingTag)>
Classic KS is not common. It mainly happens in older people of Mediterranean, Middle Eastern and eastern European ancestry. It is more common in men than in women.
Classic KS grows slowly. It is usually found only in the skin, particularly on the lower legs, ankles and soles of the feet. But it can spread to the GI tract, lymph nodes or other organs. Some people with classic KS develop a second cancer, most often non-Hodgkin lymphoma.
African Kaposi sarcoma @(Model.HeadingTag)>
African KS is also called endemic KS. It is found in parts of Africa near the equator. It is more common in young adult males.
African KS can grow slowly like classic KS, but there is also a form that grows very quickly (is aggressive). Along with causing skin tumours, African KS can grow into tissues under the skin (subcutaneous tissue) and into bone.
One form of African KS happens commonly in young children. It develops in lymph nodes and other organs. It tends to have a very poor prognosis.
KS usually appears on the skin first. The signs or symptoms of KS include:
- growths, patches or bumps on the skin that are often red, purple or brown
- patches or bumps in the mouth or throat
- swollen feet and ankles that can be painful
- enlarged lymph nodes
- GI bleeding, such as blood in the stool
- pain in the abdomen
- difficulty breathing
- weight loss
Diagnosing KS usually begins with a visit to your family doctor. Your doctor will ask you about any symptoms you have and will do a physical exam. Based on this information, your doctor may refer you to a specialist or order tests to check for KS or other health problems. These tests may be done:
Stages and risk groups @(Model.HeadingTag)>
Staging describes or classifies a cancer based on how much cancer is in the body and where it is when first diagnosed. This is often called the extent of cancer. Your healthcare team uses the stage to plan treatment and estimate the outcome (your prognosis).
There is a staging system for AIDS-related KS developed by the AIDS Clinical Trials Group. It is based on 3 factors:
- where KS is in the body – only in the skin and lymph nodes or widespread throughout the body
- health of the immune system – a high or low number of CD4 cells (a type of
lymphocyte) in the blood
- how much illness is in the body – having or not having symptoms and illness throughout the body, such as fever, night sweats or infections
Doctors then classify the KS as good risk or poor risk based on these factors.
KS is different than other soft tissue sarcomas, so it is treated differently. When deciding which treatments to offer for a KS, your healthcare team will consider:
- the type of KS
- if the KS is only in a certain area (local disease) or in many parts of the body (widespread disease)
- how well your immune system is working
- your general health
Treatments for infections and immunosuppression @(Model.HeadingTag)>
An important part of treatment for KS is to treat any infections and manage
Combined antiretroviral treatment (cART) is a combination of drugs used to treat HIV. It is also the first treatment for AIDS-related KS. Sometimes cART may be the only treatment needed or it can be combined with chemotherapy.
Stopping immunosuppressive therapy may be the first step in treating transplant-related KS. Transplant-related KS sometimes improves if immunosuppressant drugs are stopped or the dose is lowered, but this can increase the risk of organ rejection.
Antibiotics are used to treat and prevent infections with bacteria.
Surgery can be used to remove small areas of KS on the skin, especially when the KS is classified as a good risk. The following types of surgery may be used.
Surgical excision removes the cancer along with some normal tissue around it.
Curettage and electrodesiccation uses a sharp tool (called a curette) to scrape the cancer. Then the area is treated with an electrical current to destroy any remaining cancer cells.
Cryosurgery uses extreme cold to freeze and destroy tissue. Find out more about cryosurgery.
Radiation therapy @(Model.HeadingTag)>
External radiation therapy (also called external beam radiation therapy) uses a machine to direct a beam of radiation to the area of skin and a small amount of nearby tissue. It may be used to treat one or a few skin tumours in a specific area. In some cases, it may also be used to control more widespread disease.
Find out more about radiation therapy.
Topical therapy @(Model.HeadingTag)>
Topical therapy uses a cream or gel to put drugs directly on the skin. Alitretinoin (Panretin) is a topical therapy that may be used for AIDS-related KS of the skin.
Chemotherapy uses anticancer (cytotoxic) drugs to destroy cancer cells. It is usually given as a systemic therapy, which means that the drugs travel through the blood to reach and destroy cancer cells all over the body. Chemotherapy drugs used alone or in combination for KS include:
- pegylated liposomal doxorubicin (Caelyx)
- paclitaxel (Taxol)
- docetaxel (Taxotere)
- vinorelbine (Navelbine)
- gemcitabine (Gemzar)
- bleomycin (Blenoxane)
- etoposide (Vepesid, VP-16)
- vincristine (Oncovin)
A small amount of chemotherapy drug may be injected directly into the skin tumour to kill the cancer cells (called intralesional chemotherapy). Vinblastine is used most often.
Find out more about chemotherapy.
Immunotherapy uses drugs to help the body’s immune system fight cancer cells. It is sometimes used alone or in combination with chemotherapy for AIDS-related KS. Immunotherapy drugs that may be used include interferon alfa-2a, interferon alfa-2b and interleukin-12.
Find out more about immunotherapy.
Targeted therapy @(Model.HeadingTag)>
Targeted therapy uses drugs to target specific molecules (such as proteins) on or inside cancer cells to stop the growth and spread of cancer and limit harm to normal cells. It is used in some people with AIDS-related KS. Targeted therapy drugs used include imatinib (Gleevec) and bevacizumab (Avastin).
Find out more about targeted therapy.
For more detailed information on specific drugs, go to sources of drug information.
International Agency for Research on Cancer (IARC). Volume 70: Epstein-Barr virus and Kaposi's sarcoma herpesvirus/human herpesvirus 8. 1997: http://monographs.iarc.fr/ENG/Monographs/vol70/mono70.pdf.
National Cancer Institute. Kaposi Sarcoma Treatment (PDQ®) Health Professional Version. 2018: https://www.cancer.gov/types/soft-tissue-sarcoma/hp/kaposi-treatment-pdq.
National Cancer Institute. Kaposi Sarcoma Treatment (PDQ®) Patient Version. 2018: https://www.cancer.gov/types/soft-tissue-sarcoma/patient/kaposi-treatment-pdq.
Pyakurel P, Pak F, Mwakigonja AR, Kaaya E, Biberfeld P . KSHV/HHV-8 and HIV infection in Kaposi's sarcoma development. Infectious Agents and Cancer. 2007.