Pancreatic cancer starts when cells in the pancreas grow out of control. The pancreas is a gland about the size of your hand located behind your stomach. It has two main jobs: making digestive juices that help break down food, and making hormones like insulin that control blood sugar levels.
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When cancer develops in the pancreas, it usually begins in the cells that make digestive juices. This type is called ductal adenocarcinoma and accounts for about 85% of all pancreatic cancer cases. Cancer can also start in the hormone-producing cells, though this is less common.
According to the National Cancer Institute, pancreatic cancer accounts for about 3% of all cancer diagnoses in the United States, but it causes about 7% of cancer deaths. In 2024, an estimated 66,440 people were diagnosed with pancreatic cancer, and about 51,750 people died from it. The five-year survival rate is approximately 13%, though this varies based on the stage at diagnosis and other factors.
Pancreatic cancer grows differently than many other cancers. It often spreads to nearby organs and distant parts of the body before symptoms appear. This is one reason why early detection matters. When the cancer is caught while still in the pancreas, the five-year survival rate is about 48%. Once it has spread beyond the pancreas, this rate drops to 3%.
Understanding how pancreatic cancer develops helps explain why screening and awareness are important. The cancer typically progresses through stages, starting in the pancreas and potentially moving to the liver, lungs, and other organs if left undetected.
Takeaway: Pancreatic cancer is a serious disease that grows quickly and often spreads before symptoms appear. Learning about how it develops in the pancreas helps you understand why early detection could make a significant difference in outcomes.
Several factors can increase your risk of developing pancreatic cancer. Understanding these risk factors does not mean you will develop cancer if you have them—it simply means your risk may be higher than the general population.
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Age is one of the most significant risk factors. Pancreatic cancer is more common in older adults, with most cases occurring in people over age 65. The average age at diagnosis is 70 years old. However, pancreatic cancer can occur at any age.
Smoking is one of the most modifiable risk factors. People who smoke are about twice as likely to develop pancreatic cancer compared to people who have never smoked. Former smokers also have a higher risk than those who never smoked, though the risk decreases over time after quitting.
Obesity and diabetes are linked to pancreatic cancer risk. People with a body mass index (BMI) of 30 or higher have a slightly increased risk. People with type 2 diabetes, especially those diagnosed after age 50, also have an increased risk. Chronic pancreatitis—long-term inflammation of the pancreas—increases risk as well. Chronic pancreatitis can be caused by heavy alcohol use, gallstones, or genetic factors.
Family history and genetics play a role for some people. About 10% of pancreatic cancers are hereditary, meaning they run in families. People with genetic syndromes such as hereditary breast and ovarian cancer syndrome, Lynch syndrome, or familial atypical multiple mole melanoma syndrome may have higher risk. People with a family history of pancreatic cancer—especially if multiple relatives were diagnosed—should discuss screening options with their doctor.
Certain occupational exposures may increase risk. Workers in industries involving chemicals, pesticides, or metals may have slightly higher risk, though research is still ongoing in this area. Heavy alcohol use increases risk, partly because it can cause chronic pancreatitis.
Takeaway: Multiple factors can increase pancreatic cancer risk, including age, smoking, obesity, diabetes, family history, and chronic pancreatitis. Knowing your personal risk factors can help you make informed decisions about discussing screening and early detection with your healthcare provider.
One of the main challenges with pancreatic cancer is that early stages often do not cause noticeable symptoms. By the time symptoms appear, the cancer may have already advanced. However, recognizing possible warning signs and discussing them with a doctor is important.
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Abdominal pain or back pain is among the most common symptoms. The pain typically occurs in the upper abdomen and may spread to the back. It might feel worse after eating or when lying down, and may improve when you lean forward. This pain affects about 70% of people with pancreatic cancer.
Jaundice—yellowing of the skin and eyes—occurs when a tumor blocks the bile duct. The whites of your eyes may appear yellow, and your skin may take on a yellow tint. You might also notice dark urine or pale, clay-colored stools. Itching of the skin can accompany jaundice. About 70% of people with pancreatic cancer develop jaundice at some point.
Digestive problems are another warning sign. You might experience loss of appetite, nausea, vomiting, or unexplained weight loss. Some people develop new-onset diabetes or find their diabetes becomes harder to control. Loose, pale, or fatty-looking stools may indicate the pancreas is not making enough digestive enzymes.
General symptoms include fatigue, weakness, or a general feeling of not being well. Some people notice swelling in the legs or feet. Blood clots may develop in the veins of the legs, causing swelling and pain.
It is important to know that these symptoms can be caused by many different conditions, not just pancreatic cancer. However, if you experience any of these symptoms that last more than a couple of weeks, you should mention them to your doctor. Your doctor can perform tests to determine the cause. Symptoms are not a reason to panic, but they are a reason to seek medical evaluation.
Takeaway: Pancreatic cancer symptoms often appear only in later stages. While symptoms like abdominal pain, jaundice, digestive problems, and unexplained weight loss may have many causes, any symptom lasting more than a few weeks warrants discussion with your healthcare provider.
Early detection of pancreatic cancer remains challenging because there is no routine screening test recommended for the general population. Unlike mammograms for breast cancer or colonoscopy for colorectal cancer, pancreatic cancer screening is not standard practice. However, research is ongoing to develop better detection methods, and certain screening approaches may be considered for people at high risk.
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Imaging tests can help detect pancreatic cancer. CT scans (computed tomography) use X-rays to create detailed pictures of the pancreas and surrounding organs. MRI (magnetic resonance imaging) uses magnetic fields and radio waves to create images. Both can show tumors and help determine if cancer has spread. Endoscopic ultrasound (EUS) involves passing a thin tube with an ultrasound probe down the throat to get close-up images of the pancreas. This test can detect small tumors and obtain tissue samples for testing.
Blood tests may help in detection and monitoring. The CA 19-9 test measures a tumor marker—a substance produced by cancer cells—in the blood. Elevated CA 19-9 levels can suggest pancreatic cancer, but this test is not specific enough to use alone for screening. It is more often used in people already diagnosed with cancer to monitor treatment response. Other blood tests measure pancreatic enzymes and may indicate pancreatic problems.
For people with a family history of pancreatic cancer, researchers are studying whether screening with imaging and blood tests might help catch cancer earlier. Some medical centers offer screening programs for high-risk individuals. These programs typically involve annual or periodic imaging and blood tests. If you have a significant family history or genetic risk factors, discussing screening options with a gastroenterologist or oncologist may be beneficial.
Genetic testing may be recommended for people with a strong family history. If you have multiple relatives with pancreatic cancer or a personal or family history of hereditary cancer syndromes, genetic counseling and testing could help determine your risk level. Genetic counselors can explain what tests might be appropriate and what results mean for your health.
This guide is for general information only and is not medical, financial, legal, or other professional advice. For decisions specific to your situation, consult a qualified professional. See our Editorial Policy.