Pancreatic cancer (pancreatic carcinoma):
late signs, enzyme replacement & diabetes

At a glance

How commonAround 19,900 new cases a year in Germany; fourth most common cause of cancer death in both men and women, average age at diagnosis over 70
DefinitionMalignant tumour of the part of the pancreas that produces digestive juices — usually a ductal adenocarcinoma
Typical signsOften late: painless jaundice, upper abdominal and back pain, weight loss, fatty stools, newly developed diabetes
TreatmentWhere possible, surgery plus chemotherapy; otherwise chemotherapy, symptom control and early palliative care
Medicines in daily lifeEnzyme capsules with every meal, often insulin, blood thinners and painkillers — many doses, many interactions
Guideline & ICD-10German S3 guideline on exocrine pancreatic carcinoma (German Guideline Program in Oncology, AWMF 032-010OL) · C25

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1. What is pancreatic cancer?

The pancreas lies across the upper abdomen behind the stomach. It has two jobs: its exocrine part produces digestive enzymes for fat, protein and carbohydrates, and its endocrine part produces the hormones insulin and glucagon, which control blood sugar. In the vast majority of cases, pancreatic cancer arises from the duct cells of the exocrine part; specialists call it ductal adenocarcinoma.¹ Neuroendocrine tumours of the pancreas are a separate, often slower-growing disease with different treatment.

In Germany, around 19,900 people are newly diagnosed each year, women and men about equally often. Almost as many die of it each year — pancreatic cancer is the fourth most common cause of cancer death in both men and women. The relative five-year survival rate is around 11 per cent, one of the lowest of all cancers.²

These figures are sobering, but they are averages. If the tumour is found while it can still be operated on, the outlook is considerably better, and even at advanced stages treatment can gain time and quality of life. The cancer should not be confused with inflammation of the pancreas (pancreatitis) — even though chronic inflammation increases the risk of cancer and both can cause similar symptoms.


2. Types and stages: what does “operable” mean?

Where the tumour sits determines the first symptoms; how far it has grown into the surrounding blood vessels determines the treatment.¹,³

  • Head of the pancreas: the most common site. The bile duct runs through here — a tumour can compress it and cause jaundice, sometimes comparatively early.
  • Body and tail of the pancreas: tumours here often go unnoticed for a long time and only show up through pain or metastases.
ClassificationWhat it meansUsual approach
ResectableTumour without relevant contact with major blood vessels, no metastasesSurgery, followed by chemotherapy
Borderline resectableTumour touches major blood vessels; complete removal is uncertainUsually chemotherapy first, then surgery is reassessed
Locally advancedTumour surrounds important blood vessels, no distant metastasesChemotherapy, possibly radiotherapy; rarely the tumour becomes operable afterwards
MetastaticSecondary tumours, for example in the liver, peritoneum or lungsChemotherapy, symptom control, palliative care
Table scrolls to the right

By the time of diagnosis, the tumour can no longer be operated on in the majority of people affected — the main reason for the poor overall prognosis.³


3. Symptoms: why they often appear late

The pancreas lies deep in the abdomen, and a small tumour does not disrupt any function for a long time. The first signs are often inconspicuous and easily attributed to other causes:¹,³

  • Painless jaundice: yellow eyes and skin, dark urine, pale stools and often severe itching. Jaundice without pain and without fever should always be investigated promptly.
  • Upper abdominal and back pain: dull, belt-like, often worse at night or when lying down, better when leaning forward.
  • Unintentional weight loss and loss of appetite — sometimes with an aversion to certain foods and nausea.
  • Digestive problems: fatty stools (shiny, foul-smelling, hard to flush away), bloating and diarrhoea, because enzymes are missing.
  • Newly developed diabetes: especially over the age of 50, without excess weight or together with weight loss. Known diabetes that suddenly becomes hard to control can also be a sign.
  • Thromboses: a deep vein thrombosis in the leg or a pulmonary embolism with no apparent cause can be the first sign of a tumour.
New diabetes over 50 with weight loss: ask about it. The vast majority of new diabetes cases are ordinary type 2 diabetes. But if the picture does not fit — no excess weight, unintentional weight loss, upper abdominal or back pain — ask your practice specifically about the pancreas. Jaundice with fever and shivering, on the other hand, is an emergency (possible inflammation of the bile ducts): go to the emergency department immediately or call 112 (emergency number in Germany).

4. Causes and risk factors

In most people affected, no single cause can be identified. Known risk factors are:²

  • Smoking: the most important avoidable risk factor — both active and passive.
  • Severe obesity and type 2 diabetes: both increase the risk; conversely, new diabetes can also be a consequence of the tumour.
  • Chronic pancreatitis: inflammation lasting years, often due to very heavy alcohol consumption, increases the risk considerably.
  • Family and genes: pancreatic cancer in first-degree relatives, hereditary changes in genes such as BRCA1, BRCA2 or PALB2 — which are also linked to breast cancer and ovarian cancer — and hereditary pancreatitis.¹
  • Infections: Helicobacter pylori, hepatitis B and HIV are being discussed as risk factors.
  • Diet: very frequent consumption of processed meat and smoked or grilled food is suspected of increasing the risk.
Screening for everyone? No. There is no screening programme for the general population, because no test is reliable enough and the disadvantages would outweigh the benefits. The blood marker CA 19-9 is not suitable for early detection either. For people with a very high familial or hereditary risk, there are specialised centres and programmes — ask about them if several relatives are affected.¹ According to current knowledge, there is no evidence that common medicines trigger pancreatic cancer; medicine-induced acute pancreatitis is a different matter.

5. Diagnosis: from suspicion to tumour board

The aim of the tests is to clarify whether there is a tumour, how far it has spread and whether it can be operated on.¹

  • Ultrasound: often the first step, showing for example blocked bile ducts; however, a normal ultrasound does not rule out a tumour.
  • CT with contrast agent: the most important test for assessing the tumour, contact with blood vessels and metastases; MRI in addition, especially for the liver.
  • Endoscopic ultrasound: ultrasound from the inside via the stomach, very precise for small tumours; tissue can be taken at the same time. A tissue sample is not always necessary before planned surgery.
  • Laparoscopy: for certain findings before surgery, to detect small metastases on the peritoneum.
  • Relieving the bile duct: in jaundice, often via a small plastic or metal stent inserted endoscopically.
  • Blood tests: CA 19-9 is used to monitor progress during treatment, not for diagnosis. In addition, liver, blood sugar and nutritional values.
  • Molecular and hereditary testing: at an advanced stage, tumour tissue can be tested for rare changes that can be treated in a targeted way; many people are also asked about hereditary changes such as BRCA.
  • Tumour board: a team from gastroenterology, surgery, oncology, radiology, radiotherapy and pathology agrees on the recommendation — ideally at a certified pancreatic cancer centre.

Many terms, many appointments: a list of questions and your current medicines helps — see Preparing for a doctor's appointment.

6. Treatment: surgery, chemotherapy, palliative care

Treatment depends on the stage, your general condition and your own goals. It is planned at the tumour board; you make the decision together with your treatment team. A cure is only possible if the tumour can be removed completely — and even then, chemotherapy is part of it.¹

Operable Surgery and chemotherapy
Surgery
For tumours in the head of the pancreas, usually the so-called Whipple procedure (partial pancreatoduodenectomy): the head of the pancreas, the duodenum, the gallbladder and parts of the bile duct are removed, often preserving the stomach. For tumours in the tail, the left part of the gland is removed together with the spleen. Such operations belong in hospitals with extensive experience.
Chemotherapy after surgery
For about six months, to reduce the high risk of recurrence. Patients who are fit enough usually receive a multi-drug combination (modified FOLFIRINOX); others receive treatment based on gemcitabine, for example combined with capecitabine.¹
Borderline / locally advanced Chemotherapy first, then reassess
Chemotherapy before surgery
It aims to shrink the tumour and treat undetected metastases at the same time. Afterwards, it is checked whether surgery is possible; occasionally radiotherapy is added.
Metastatic Time and quality of life
Chemotherapy
Depending on general condition, FOLFIRINOX or gemcitabine with nab-paclitaxel, and for people in a weakened condition also gemcitabine alone. The aim is to slow growth and relieve symptoms.¹
Targeted therapy for particular features
With a hereditary BRCA mutation, maintenance treatment with a PARP inhibitor may be considered after successful platinum-based chemotherapy; other rare changes have their own active ingredients. This applies only to a small proportion of those affected.
Early palliative care
The guideline recommends involving it early — alongside chemotherapy, not only afterwards. It takes care of pain, nutrition, nausea, jaundice and anxiety and can measurably improve quality of life.¹,⁴

7. Supportive medicines: pain, thrombosis, nausea

Alongside chemotherapy, many people need several supportive medicines — and often also take long-term medication for high blood pressure, diabetes or heart disease. This makes planning and checking for interactions particularly important.⁵

Pain: enough, and on schedule

Cancer pain is treated according to a fixed schedule, not only when needed. Commonly used are metamizole and opioids such as morphine, oxycodone or a fentanyl patch. Opioids almost always cause constipation; that is why a laxative such as macrogol belongs with them from the start. For severe pain, blocking the nerve network behind the pancreas (coeliac plexus) can help reduce the need for opioids.⁴

Thrombosis: high risk, special rules

Pancreatic cancer is one of the cancers with the highest risk of thrombosis and pulmonary embolism. It is treated with a low-molecular-weight heparin such as enoxaparin or with an anticoagulant in tablet form; which one is suitable depends, among other things, on the bleeding risk, blood values and interactions with chemotherapy.⁵ Everyday tips in the guide Living with blood thinners.

Nausea and cortisone

Nausea caused by chemotherapy can be prevented effectively, for example with ondansetron, often combined with dexamethasone. The cortisone can make blood sugar rise sharply — if you have diabetes, measure more often on these days.⁵

These signs are an emergency. A fever of 38 °C or higher during chemotherapy, fever with shivering when a bile duct stent is in place, sudden shortness of breath or chest pain, a badly swollen leg, vomiting blood or black stools: contact your centre's emergency number, the emergency department or 112 immediately. Do not stop opioids, blood thinners or insulin on your own — withdrawal symptoms, thromboses or blood sugar going out of control can be the result; see Stopping medications.

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8. Enzyme replacement: taking capsules correctly

If the tumour blocks the pancreatic duct or part of the gland has been removed, digestive enzymes are missing. This exocrine pancreatic insufficiency is very common and shows itself through fatty stools, bloating, abdominal cramps and weight loss despite eating enough. The solution is enzyme capsules containing pancreatin, which replace the missing enzymes. The guideline expressly recommends enzyme replacement when these symptoms are present, because it improves nutritional status and quality of life.¹,⁶

  1. With every meal: the capsules only work if they reach the intestine together with the food — so take them with your meal, not before it or hours afterwards. With larger meals, the dose can be split between the beginning and the middle of the meal.⁶
  2. With snacks too: every snack containing fat or protein also needs enzymes, usually at a lower dose. A glass of water or tea without milk does not need any.
  3. Do not chew: the capsules contain gastro-resistant pellets. If you cannot swallow them, open the capsule and take the contents, as described in the package leaflet, with a little soft, slightly acidic food such as apple sauce — without chewing.⁶
  4. Dose by effect: the amount is given in lipase units and adjusted by the practice to your meals and symptoms. If fatty stools and weight loss persist, the dose is often too low — report this rather than going hungry on a low-fat diet.
  5. Keep an eye on vitamins: when fat digestion is impaired, the fat-soluble vitamins A, D, E and K can be lacking; they are checked and replaced if needed.
Timing is everything here. Enzyme capsules are one of the few medicines whose effect depends entirely on timing — not on the time of day, but on the meal. If the effect is too weak despite an adequate dose, the practice may additionally prescribe an acid blocker such as pantoprazole, so that the enzymes are not broken down too early by stomach acid. More on medicines and mealtimes in the guide Medications before or after eating.

9. Diabetes caused by pancreatic cancer

The tumour or an operation can also destroy the cells that produce insulin. This results in a form of diabetes that differs from ordinary diabetes — specialists call it pancreatogenic diabetes or type 3c diabetes.¹,³

  • Glucagon is missing too: this hormone raises blood sugar again when it is too low. If it is missing, for example after removal of the whole pancreas, hypoglycaemia develops faster and is more severe. Always keep glucose tablets to hand.
  • Insulin is often needed: always after removal of the whole gland, and frequently otherwise. How injecting works in everyday life is explained in the guide Injecting insulin correctly; information on the active ingredient under insulin.
  • Measure blood sugar more closely: appetite fluctuates, meals are skipped, cortisone days push sugar up — the insulin dose often needs adjusting. Tips in the guide Measuring blood sugar correctly.
  • Enzymes and insulin go together: without enzyme replacement, food is poorly absorbed and blood sugar rises less than expected — hypoglycaemia becomes a risk. If you take both, clarify how to coordinate them with your practice.
  • Adjust the targets: at an advanced stage, the priority is not perfect long-term control but avoiding hypoglycaemia and very high blood sugar. Strict dietary rules are then usually not sensible.

If you already had type 2 diabetes and take tablets such as metformin, have your medication reviewed at the start of cancer treatment — weight loss, loss of appetite and chemotherapy change what you need.


10. Everyday life with pancreatic cancer

  • Maintaining weight comes first — eat energy- and protein-rich food, ideally several small meals. Involve nutritional counselling early, not only once there is marked weight loss.³
  • Keep a complete medication plan — chemotherapy, enzymes, insulin, heparin, painkillers and laxatives, long-term medication and anything you buy yourself. Instructions under Creating a medication plan.
  • Note stools and symptoms — fatty stools, pain, blood sugar and weight, with the date. This helps when adjusting enzymes, insulin and painkillers.
  • Keep moving — suitably adapted exercise maintains strength and lowers the risk of thrombosis, even during chemotherapy.
  • Discuss herbal products and supplements — some products affect chemotherapy or blood clotting, see Supplements and medications.
  • Accept help — psycho-oncology services, cancer counselling centres, the hospital social services and outpatient palliative care teams. Relatives can come along to appointments and should know the centre's emergency number.

Pancreatic cancer is a serious diagnosis. That is precisely why anything that eases everyday life is worthwhile: clear plans, fewer forgotten doses, less guesswork about symptoms — and time for what matters to you.

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FAQ: Common questions about pancreatic cancer

Early signs are often absent or non-specific. Possible signs include painless jaundice with dark urine and pale stools, upper abdominal and back pain, unintentional weight loss, fatty stools and newly developed diabetes from around the age of 50. Such symptoms should be checked by a doctor.
A cure is only possible if the tumour can be removed completely by surgery, and even then chemotherapy is part of the treatment because the risk of recurrence is high. In most people, the tumour can no longer be operated on at the time of diagnosis. Chemotherapy and palliative care can then gain time and relieve symptoms.
Enzyme capsules are taken together with every meal and every snack containing fat or protein; with larger meals, the dose is split between the beginning and the middle of the meal. The capsules are not chewed. If fatty stools or weight loss persist, the dose should be adjusted with the practice.
Rarely, yes. The vast majority of new diabetes cases are ordinary type 2 diabetes. However, if diabetes develops after the age of 50 without excess weight, or together with weight loss and abdominal or back pain, the pancreas should be examined specifically.
Yes, but only with permanent replacement of both functions. Digestive enzymes are taken as capsules with every meal, and insulin has to be injected. Because the hormone glucagon is also missing, the risk of severe hypoglycaemia is increased, which is why glucose tablets should always be to hand.
No. CA 19-9 can also be raised in harmless conditions such as a blocked bile duct and is normal in some tumours. The marker is therefore only used to monitor progress during treatment, not for early detection or a definite diagnosis.
In a small proportion of those affected, hereditary changes play a role, for example in the genes BRCA1, BRCA2 or PALB2, or there is hereditary pancreatitis. If several relatives are affected, genetic counselling may be worthwhile. Specialised early detection programmes exist for people at very high risk.

Sources

  1. German S3 guideline on exocrine pancreatic carcinoma, German Guideline Program in Oncology (German Cancer Society, German Cancer Aid, AWMF), AWMF reg. no. 032-010OL, version 3.1 (2024) — German source. awmf.org
  2. German Centre for Cancer Registry Data at the Robert Koch Institute: Pancreatic cancer, data for 2023. Accessed 2026 — German source. krebsdaten.de
  3. Cancer Information Service of the German Cancer Research Center (Krebsinformationsdienst, DKFZ): Pancreatic cancer — symptoms, treatment, nutrition. Accessed 2026 — German source. krebsinformationsdienst.de
  4. German S3 guideline on palliative care for patients with incurable cancer, German Guideline Program in Oncology (AWMF reg. no. 128-001OL, current version) — German source. awmf.org
  5. German S3 guideline on supportive therapy for cancer patients, German Guideline Program in Oncology (AWMF reg. no. 032-054OL, current version) — German source. awmf.org
  6. Summaries of Product Characteristics (SmPCs) for medicines containing pancreatin (taking with meals, use in swallowing difficulties) — German source. fachinfo.de

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Medical disclaimer: This article is for general information and does not replace medical advice, diagnosis or treatment. Painless jaundice, unintentional weight loss or new diabetes with abdominal or back pain should be checked by a doctor promptly; a fever of 38 °C or higher during chemotherapy, or fever with shivering when a bile duct stent is in place, is an emergency. Do not stop opioids, blood thinners or insulin on your own. The choice of medicine and its dose are always set individually by the treating practice. Last updated: October 2026.