You should have one main doctor who coordinates your care. This is often:

• a medical oncologist (if chemotherapy is your main treatment)
• a surgeon (if surgery is planned)
• a gastroenterologist (if you're having tests to diagnose the cancer)

The rest of your multidisciplinary team will be made up of a mix of medical specialists, allied health professionals and supportive care professionals.

Each team member brings special skills to make sure all parts of your care are looked after. They meet regularly to talk about your case and agree on the best treatment approach.

The make-up of this multidisciplinary team may change at different stages of your treatment, but may include:

To make an informed decision, it helps to know as much as you can about your treatment choices. Your treatment team will explain:

• the different treatment options available to you
• the goals of each treatment (for example, cure, control, or symptom relief)
• the benefits and risks of each option
• possible side effects and how they might affect you
• what treatment involves — how long it takes, where it happens, and how often
• how it might affect your daily life

Everyone’s situation is different. When making treatment decisions, you might want to think about:

• your personal goals and what matters most to you
• your overall health and how fit you feel
• the side effects and how they could affect your quality of life
• practical issues such as travel, time off work, or caring for family
• your own values, beliefs and preferences

It can help to write down your questions before appointments. You might like to ask:

• what treatment do you recommend, and why?
• what is the goal of this treatment?
• what are the benefits and possible risks?
• what side effects could I expect?
• how will treatment affect my everyday life?
• are there other treatment options?
• what happens if I choose not to have treatment?
• is there a clinical trial that might be suitable for me?
• how much will treatment cost?
• who should I contact if I have questions or feel unwell?

Although some treatments need to start quickly, you usually have time to:

• ask questions and get clear answers
• talk about your options with your family or friends
• ask for a second opinion if you want one
• think about what matters most to you before deciding.

Taking time to understand your options can help you feel more confident about your decisions.

You may be able to have surgery if the cancer is only in your pancreas or close by, and it hasn’t grown into major blood vessels. You also need to be well enough to manage a big operation.

Doctors use certain words to describe whether surgery is possible:

• Resectable (operable): The cancer can be removed with surgery.
• Borderline resectable: Surgery might be possible after chemotherapy to shrink the tumour.
• Locally advanced or metastatic: The cancer has spread too far, so surgery isn’t an option.

The type of surgery depends on where the cancer is in your pancreas.

Whipple procedure (Pancreaticoduodenectomy)

This is the most common operation when the cancer is in the head of the pancreas.

The surgeon removes:

• the head of the pancreas
• the first part of the small intestine (duodenum)
• the gallbladder and part of the bile duct
• sometimes the bottom part of the stomach.

The remaining pancreas, bile duct and stomach are reconnected to the small intestine so your digestive system still works.

Distal pancreatectomy

This type of surgery is used when the cancer is in the body or tail of the pancreas.

The surgeon removes:

• the body and tail of the pancreas
• usually the spleen.

The head of the pancreas stays in place.

Total pancreatectomy

This operation removes the whole pancreas. It may also remove the gallbladder, part of the bile duct, parts of the stomach and small intestine, and often the spleen.

After this surgery, your body will no longer make insulin, so you’ll need insulin injections for life.

Bypass surgery

If the cancer can’t be removed, surgery may be done to ease symptoms.

This might include:

• creating a new path for food to pass from the stomach to the bowel
• creating a new path for bile to flow around a blockage.
  
  

Stent insertion

Instead of bypass surgery, a thin tube called a stent can be placed in a blocked bile duct to keep it open and relieve jaundice.

Before surgery

• You’ll have several tests to check you’re ready for the operation.
• You’ll meet your surgical team to talk about the benefits, risks and what recovery will look like.

During your hospital stay

• Most people stay in hospital for 1–2 weeks after surgery for pancreatic cancer.
• You may start your recovery in an intensive care or high-dependency unit.
• You’ll slowly begin to eat and drink again.
• Your team will help manage pain and watch for any problems.

Recovery at home

• Recovery can often take a few months. You’ll need some help at home, and it’s important to build up your strength slowly.
• Your care team will schedule follow-up appointments to check your progress.
• Surgery changes how your pancreas works. You might:
• Notice changes in digestion
• need pancreatic enzyme supplements (like Creon^®)
• experience blood-sugar changes or diabetes
• notice appetite and weight changes.

Your healthcare team will help you manage these effects and adjust your diet if needed. A dietitian can support you with meal ideas and supplements.

Having pancreatic surgery is a big step. It’s normal to feel anxious or tired.
You can ask for help from your care team, social worker or cancer support groups.

Pancare’s Support service can connect you with others who’ve been through surgery and recovery.

Your oncologist may recommend chemotherapy:

• before surgery (called neoadjuvant therapy) to shrink the tumour and make surgery easier.
• after surgery (called adjuvant therapy) to lower the chance of the cancer coming back.
• as your main treatment when surgery isn’t possible.

Chemotherapy can be given in two main ways.

• Through a drip (IV chemotherapy). The medicine goes into a vein through a drip, usually in a hospital or cancer clinic. Each session can take a few hours, depending on your treatment plan.
• As tablets or capsules (oral chemotherapy). Some chemotherapy medicines come as tablets or capsules you take at home. Your oncologist will explain exactly when and how to take them.

Your chemotherapy plan

Your oncologist will design a plan based on:

• the stage of your cancer
• your overall health
• whether you’ve had surgery
• previous treatments
• clinical trials that might be suitable.

Most plans use a combination of drugs that work together to fight cancer cells.

Chemotherapy is usually given in cycles. This means you’ll have a period of treatment followed by a rest period so your body can recover.

A full course of chemotherapy often lasts several months. Your care team will explain the exact schedule for you.

Access devices

If you’re having IV chemotherapy through a drip, your doctor may recommend a device to make treatment easier. This might be:

• a PICC line: a soft tube placed in a vein in your arm and threaded near your heart. It stays in during your treatment so you don’t need needles each time.

• a Port (Port-a-Cath): a small device placed under the skin of your chest that connects to a vein. It’s accessed with a special needle and can stay in for months.

These devices help protect your veins and make treatment more comfortable.

Monitoring during treatment

You’ll have regular check-ups to make sure chemotherapy is working safely.
 These may include:

• blood tests to check your blood counts and organ function
• scans to see how the cancer is responding
• check-ins to talk about how you’re feeling and any side effects

Side effects and how to manage them

Chemotherapy can affect healthy cells too, which causes side effects. Not everyone gets the same effects, and most can be managed well.

Common side effects include:

• feeling tired or weak
• feeling sick (nausea) or vomiting
• loss of appetite or changes in taste
• hair thinning or loss
• diarrhoea or constipation
• mouth sores
• numbness or tingling in your hands and feet
• higher risk of infections.

Your team can help by:

• prescribing anti-sickness or infection-preventing medicines
• adjusting your chemotherapy dose if needed
• providing nutrition and pain-management advice
• offering emotional and practical support.

Always tell your nurse or doctor about any side effects. There are often ways to make you feel more comfortable.

It’s normal to feel tired or emotional during treatment.

Your healthcare team can help with symptom control, nutrition, and emotional wellbeing.

You can also reach out to Pancare Support for practical advice, counselling, and connections with others living with pancreatic cancer.

Your doctor may suggest radiotherapy:

• before surgery, alongside chemotherapy to shrink the tumour so surgery is easier.
• after surgery to treat any remaining cancer cells near where the tumour was removed.
• to slow down the growth of cancer that can’t be removed by surgery.
• to help ease pain or other symptoms in advanced pancreatic cancer.

Radiotherapy targets cancer cells very precisely to reduce harm to healthy tissue around the pancreas.

Modern machines let doctors:

• aim radiation beams directly at the tumour
• protect nearby organs such as the stomach and bowel
• give small doses over several sessions to lower the risk of side effects.

You won’t see or feel the radiation, but it works inside your body to damage the DNA of cancer cells so they can’t keep growing.

Radiotherapy is often used together with a small dose of chemotherapy. This is called chemoradiation. The chemotherapy makes cancer cells more sensitive to radiation, helping the treatment work better.

Your oncologist will discuss whether this approach is suitable for you.

Before treatment

• You’ll have a planning session to prepare for radiotherapy.
• You might have a CT scan to help your team map out the exact treatment area.
• Small dots or tattoos may be placed on your skin so the radiation can be aimed accurately each time.
• Your team will explain how many treatments you’ll need and what to expect.

During treatment

• Treatment usually happens once a day, Monday to Friday.
• Each visit lasts about 15–30 minutes, but the radiation itself takes only a few minutes.
• You’ll lie still on a treatment bed while the machine moves around you.
• You won’t feel the radiation, and you’ll be able to go home afterwards.
• Most people have treatment for several weeks.

Side effects and how to manage them

Side effects usually appear slowly during treatment and improve a few weeks after it finishes. Everyone reacts differently, but common effects include:

• feeling tired
• skin redness or irritation in the treated area
• nausea or loss of appetite
• diarrhoea or softer bowel motions
• discomfort or a warm feeling in the abdomen

Your radiation oncology team will help you manage side effects. They can give advice about:

• gentle skin care
• anti-nausea or diarrhoea medicines
• eating well and maintaining energy
• when to contact your doctor if you’re worried.

It’s normal to feel tired or emotional during treatment.

Your healthcare team can help with symptom control, nutrition, and emotional wellbeing.

You can also reach out to Pancare Support for practical advice, counselling, and connections with others living with pancreatic cancer.

Taking part in a clinical trial can give you the chance to try a new approach that may work better than standard care. You’ll be closely monitored by expert doctors and nurses who specialise in pancreatic cancer.

Even if the treatment being tested doesn’t benefit you directly, your participation helps researchers learn more about the disease and improve care for future patients. Many people find this sense of contributing to progress reassuring and empowering.

There are many different types of clinical trials. Some test new chemotherapy drugs or combinations, while others explore targeted therapies that act on specific changes in cancer cells.

Researchers are also studying new ways to use immunotherapy to help the body’s own immune system fight cancer.

Other trials look at surgical techniques, how to better manage symptoms or side effects, or how to detect pancreatic cancer earlier.

Each trial has its own entry requirements, called eligibility criteria. These might include the type and stage of your cancer, your previous treatments, your general health, and sometimes genetic features found in your tumour. Your healthcare team can explain which kinds of studies are currently running and whether one may be right for you.

If you’d like to explore current pancreatic cancer trials, speak to your oncologist or visit trusted websites such as australiancancertrials.gov.au or the Australasian Gastro-Intestinal Trials Group.

You can also contact the Pancare Foundation for guidance and information about studies in Australia.

Complementary therapies are used alongside standard medical treatments such as chemotherapy, surgery or radiotherapy. They aim to help you relax, manage symptoms, and improve your quality of life. Examples include meditation, yoga, massage, acupuncture, and relaxation techniques.

Alternative therapies, on the other hand, are used instead of standard medical treatments. These approaches have not been proven to treat cancer and can sometimes be harmful or interfere with your care.

For this reason, alternative therapies are not recommended as a replacement for evidence-based treatment.

Some complementary therapies can be safely used to help with relaxation or symptom relief, as long as your healthcare team agrees.

• For relaxation and wellbeing: Gentle exercise, yoga, meditation, mindfulness, aromatherapy, massage (with your doctor’s approval), music therapy, and art therapy can help reduce stress and improve mood.
• For specific symptoms: Acupuncture and acupressure wristbands may help reduce nausea or pain. Some people find ginger tea or tablets helpful for nausea.
   Simple breathing and relaxation exercises can ease anxiety and support sleep.

It’s common to wonder whether vitamins, minerals, or herbal products could help. Some may be safe, but others can interfere with chemotherapy or other cancer treatments.

Always tell your healthcare team about any supplements you’re taking or thinking about taking. They can check for possible interactions and advise what’s safe.

Remember:

• High doses of some vitamins can be harmful.
• ‘Natural’ doesn’t always mean safe.
• Many products make claims that are not supported by science.

If in doubt, ask your doctor, pharmacist or dietitian before starting anything new.

Before starting any new therapy, take time to check that it’s safe and worthwhile.

Talk to your healthcare team. They need to know everything you’re using. You can also ask:

• Is this safe to use with my cancer treatment?
• What are the possible risks or side effects?
• What evidence supports this therapy?
• How much will it cost and how often would I need it?

Every person’s recovery is different. Your healthcare team will create a personalised follow-up plan that explains:

• Who your main contact person is (such as a nurse or specialist)
• How often you’ll need check-ups and who you’ll see
• Which tests you may need and how often they’ll be done
• What to expect at each visit

You may have blood tests (including tumour markers like CA 19-9), and CT or MRI scans from time to time to check for any changes.

These tests help your doctors see how you’re healing and detect any possible signs of the cancer returning early.

Some people continue to experience side effects after treatment, such as fatigue, digestive changes, or problems with appetite.

Your care team will support you to manage these issues and maintain your strength.

Your doctor will tell you about symptoms that may need to be checked quickly.

These might include:

• new or worsening pain in your tummy or back
• unexpected weight loss or loss of appetite
• jaundice (yellowing of your skin or eyes)
• ongoing tiredness that doesn’t improve with rest
• changes in your bowel habits
• new lumps, swelling or discomfort anywhere in your body

If you notice any of these symptoms, or anything that worries you, contact your healthcare team or GP as soon as possible.

Recovery takes time, both physically and emotionally. Keep communicating with your care team and let them know how you’re feeling.

Gentle physical activity, a balanced diet, rest, and emotional support from friends, family, or a counsellor can all make a big difference.

If you’d like extra support, Pancare Support can connect you with nurses, counsellors, dietitians and others who understand what you’re going through.