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Cholangiocarcinoma (Bile Duct Cancer)

Cholangiocarcinoma, or bile duct cancer, is a rare form of cancer. It often affects older adults

and has usually spread beyond the bile ducts by the time it’s diagnosed. Treatment usually

involves a combination of surgery, chemotherapy or radiation therapy.

Most people receive a cholangiocarcinoma diagnosis after the cancer has already spread

outside of their bile ducts. It’s difficult to treat and the prognosis (chance of recovery) is

usually poor. However, a growing number of targeted therapies and clinical trials are starting

to change that.

Are there different types of cholangiocarcinoma?

There are three types of cholangiocarcinoma:

Extrahepatic cholangiocarcinoma is bile duct cancer outside the liver. Cancer may be in the

ducts as they exit the liver, or in the ducts when they end in the small intestine. This is the

most common type of bile duct cancer. A subset within extrahepatic cholangiocarcinoma is

hilar cholangiocarcinoma, meaning a bile duct cancer that is outside the liver, but starts in the

hilum, which is the area where the bile ducts and important blood vessels connect with the

liver.

Intrahepatic cholangiocarcinoma is bile duct cancer inside the liver. This should not be

confused with liver cancer, which is more often referred to as hepatocellular carcinoma, or

HCC.

Gallbladder canceris cholangiocarcinoma that starts in the gallbladder.

Who is at risk of getting cholangiocarcinoma?

In the United States, Hispanic Americans are at a higher risk of cholangiocarcinoma. You

may also be more likely to develop cholangiocarcinoma if you have:

 Abnormalities where the bile duct and pancreatic duct meet.

 Bile duct stones or choledochal cyst disease (bile duct cysts).

 Chronic ulcerative colitis.

 Cirrhosis of the liver.

 Clonorchiasis (infection with a Chinese liver fluke parasite).

 Hepatitis B or Hepatitis C.

 Human immunodeficiency virus (HIV).

 Inflammatory bowel disease (IBD).

 Non-alcohol related fatty liver disease.

 Primary sclerosing cholangitis (inflammation and scarring block the bile ducts).

Additional risk factors include:

 Alcohol use disorder.

 Diabetes.

 Exposure to toxins.

 Obesity.

 Smoking.

How common is cholangiocarcinoma?

Cholangiocarcinoma is rare. About 8,000 people in the U.S. develop this cancer each year.

It’s most common in older people around age 70.

Symptoms and Causes

What causes cholangiocarcinoma?

Experts don’t know exactly what causes cholangiocarcinoma. The risk factors suggest that

health conditions that cause chronic (long-term) inflammation in the bile ducts may play a

role in the development of this cancer. Persistent damage like inflammation can also lead to

DNA changes, which may change the way certain cells grow, divide and behave. These

changes probably aren’t inherited, which means parents don’t pass them to their children.

Instead, the changes likely happen during a person’s lifetime.

What are the symptoms of cholangiocarcinoma?

Bile duct cancer symptoms include:

 Abdominal pain.

 Dark urine.

 Fever.

 Itchy skin.

 Jaundice (skin and whites of eyes turn yellow).

 Light-colored stool.

 Nausea and vomiting.

 Unexplained weight loss.

Diagnosis and Tests

How is cholangiocarcinoma diagnosed?

Your healthcare provider evaluates your symptoms, reviews your medical history and does a

physical exam. Tests for cholangiocarcinoma may include:

Liver function tests: These liver tests check your blood for high levels of substances that

might indicate your liver isn’t working as it should or there is a bile duct blockage, such as

elevated liver enzymes.

Tumor marker tests: These tests check your blood or urine for proteins and other substances

that could mean you have cancer.

Abdominal ultrasound: An abdominal ultrasound uses sound waves to create pictures of your

liver, pancreas and gallbladder. This may be the first imaging exam you have if your

healthcare provider suspects bile duct cancer.

Magnetic resonance cholangiopancreatography (MRCP): MRCP is a specialized imaging

exam that uses an MRI machine. It creates detailed pictures of the liver, bile ducts,

gallbladder, pancreas and pancreatic duct.

Endoscopic retrograde cholangiopancreatography (ERCP): ERCP uses an endoscope and a

catheter (thin, flexible tubes) to examine your bile ducts. The endoscope goes into your

mouth and down to your small intestine while you’re sedated (in a light sleep). The catheter

delivers contrast dye to outline the shape of your bile ducts on X-rays. If you have a bile duct

blockage, a stent device can be placed during an ERCP in the blocked bile duct to open it

back up.

Percutaneous transhepatic cholangiography (PTC): A PTC creates X-rays of your bile ducts

like an ERCP. But instead of an endoscope and catheter, your healthcare provider delivers
contrast dye by inserting a needle directly into your bile ducts and liver. A PTC is usually

only for people who can’t have an ERCP.

If imaging and lab tests indicate cancer, your healthcare provider will perform a biopsy. A

biopsy is a procedure to take a sample of tissue from your body. A pathologist examines the

tissue under a microscope in a laboratory to check for cancer. Your healthcare provider can

take bile duct tissue samples during an ERCP, PTC or by using a small needle through the

skin.

How is cholangiocarcinoma staged?

A biopsy tells your healthcare provider if you have cancer, but it can also tell them the

cancer’s stage. Staging is the process of finding out how much cancer is in your body. This

information helps your healthcare provider plan treatment. For bile duct cancer, staging looks

at the size of the tumor and whether cancer has spread from the bile ducts to the:

Blood vessels.

Lymph vessels and lymph nodes.

Organs near the bile ducts, such as the liver or gallbladder.

Distant organs, such as the lungs, bones or abdominal cavity (called the peritoneum).

Management and Treatment

How is cholangiocarcinoma treated?

Your treatment plan for cholangiocarcinoma depends on the location of the cancer and if it

has spread. Surgery can treat early bile duct cancers that haven’t spread. But most bile duct
cancers have spread by the time they’re diagnosed. In these cases, your healthcare provider

may recommend a combination of multiple treatments.

How does surgery treat cholangiocarcinoma?

Your options for bile duct cancer surgery may include:

Bile duct removal to get rid of part of the bile duct if the cancer hasn’t spread.

Partial hepatectomy to remove part of the bile duct and sections of the liver.

Whipple procedure to remove the bile duct, gallbladder and part of the pancreas, stomach and

small intestine.

Liver transplant to replace the liver with a donor liver, though this is only for early-stage

cancers and it may be difficult to find a donor.

Palliative surgery to ease symptoms of cancer by removing blockages in the bile duct. Your

healthcare provider may place a stent (small, hollow tube) in your bile duct to help it drain

into your small intestine or place a drain that connects to a bag outside your body.

How does radiation therapy treat cholangiocarcinoma?

Radiation therapy uses powerful beams of radiation to destroy tumors. You might receive

radiation therapy after surgery to kill any remaining cancer cells. Or your healthcare provider

may suggest it before surgery to shrink tumors before removing them. Radiation can also be

delivered through transarterial radioembolization (TARE), which uses a catheter to implant

tiny beads of radiation (often referred to as “Y90”) in the blood vessels supplying the tumor.
The beads block the vessel to prevent blood from getting to the tumor. At the same time, the

beads release radiation to shrink the tumor.

How does chemotherapy treat cholangiocarcinoma?

Chemotherapy (chemo) uses drugs to destroy cancer. Systemic chemotherapy that goes

through your entire body can be used to shrink your tumor to make surgery possible. If the

cancer is too advanced for surgery, chemotherapy is used to prolong life and reduce the

symptoms of the cancer. In some cases, procedures can be done to deliver chemo directly to

your bile duct:

Transarterial chemoembolization (TACE), which uses a catheter to implant tiny beads of

chemo in the blood vessels supplying the tumor. The beads block the vessel to prevent blood

from getting to the tumor. At the same time, the beads release chemo medications to shrink

the tumor.

Hepatic artery infusion (HAI), which uses a surgically implanted pump to inject chemo

directly into the main artery that brings blood to the liver. It’s controversial whether these are

truly effective or not.

How does targeted therapy treat cholangiocarcinoma?

Targeted therapies target specific parts of cancer cells. Some people with bile duct cancer

that’s the result of an abnormal gene have specific proteins on their cancer cells. Targeted

therapies can attack these cells to keep them from dividing.

How does immunotherapy treat cholangiocarcinoma?

Immunotherapy helps your body’s own immune system fight cancer. In bile duct cancer,

some cancer cells contain a protein that prevents immune cells from attacking the cancer.

Immunotherapy disables the proteins so immune cells can do their job better.

Prevention

How can I prevent cholangiocarcinoma?

There’s no way to completely prevent bile duct cancer, but you may be able to reduce your

risk by:

 Avoiding viruses such as hepatitis B, hepatitis C and HIV.

 Getting vaccinated against hepatitis B.

 Limiting the amount of alcohol you drink.

 Maintaining a healthy body weight.

 Quitting smoking.

What is the prognosis for people with cholangiocarcinoma?

The outlook (prognosis) for people with cholangiocarcinoma is usually poor. The five-year

survival rate for bile duct cancer that hasn’t spread outside of the bile ducts is 10% to 15%.

This rate drops to 2% if the cancer spreads to areas of the body that are far from the bile

ducts, such as the lungs. But newer treatments mean these rates will improve over time.

Cholangiocarcinoma is cancer of the bile ducts. It’s a rare disease that’s more common in

older people. You have a higher risk of cholangiocarcinoma if you have certain viruses or
chronic inflammation in your bile ducts or liver. This type of cancer usually requires a

combination of treatments including surgery, radiation therapy or chemotherapy.