Non-functional Pancreatic Neuroendocrine Tumours (pNETs)

Pancreatic neuroendocrine tumours (pNETs), or islet cell tumours, are rare carcinomas (cancers arising from bone and soft tissue lining the organs) that develop in the pancreas. The pancreas is a long, flat organ that sits between the stomach and the spine. It has two primary functions; endocrine function, which is responsible for secreting hormones (such as insulin) to control blood sugar levels, and exocrine function, which produce pancreatic enzymes that aid in digestion. This page will focus on non-functional pNETs.

Neuroendocrine cancers are a complex group of tumours that develop in the neuroendocrine system, which is responsible for regulating important bodily functions such as heart rate, blood pressure and metabolism. They most commonly develop in the gastro-intestinal tract, pancreas, and the lungs; however, they can develop anywhere in the body. These tumours develop from neuroendocrine cells, which are responsible for receiving signals from the nervous system and producing hormones and peptides (small proteins) in response.

pNETs has a prevalence in males and are generally diagnosed in people over 55; however, people of any age and sex can develop this disease.

Treatment

If a pNET is detected, it will be staged and graded based on size, metastasis, and how the cancer cells look under the microscope. Staging and grading helps your doctors determine the best treatment for you.

Cancers can be staged using the TNM staging system:

  • T (tumour) indicates the size and depth of the tumour.
  • N (node) indicates whether the cancer has spread to nearby lymph nodes.
  • M (metastasis) indicates whether the cancer has spread to other parts of the body.

This system can also be used in combination with a numerical value, from stage 0-IV:

  • Stage 0: this stage describes cancer cells in the place of origin (or ‘in situ’) that have not spread to nearby tissue.
  • Stage I: cancer cells have begun to spread to nearby tissue. It is not deeply embedded into nearby tissue and had not spread to lymph nodes. This stage is also known as early-stage cancer.
  • Stage II: cancer cells have grown deeper into nearby tissue. Lymph nodes may or may not be affected. This is also known as localised cancer.
  • Stage III: the cancer has become larger and has grown deeper into nearby tissue. Lymph nodes are generally affected at this stage. This is also known as localised cancer.
  • Stage IV: the cancer has spread to other tissues and organs in the body. This is also known as advanced or metastatic cancer.

Cancers can also be graded based on the rate of growth and how likely they are to spread:

  • Grade I: cancer cells present as slightly abnormal and are usually slow growing. This is also known as a low-grade tumour.
  • Grade II: cancer cells present as abnormal and grow faster than grade-I tumours. This is also known as an intermediate-grade tumour.
  • Grade III: cancer cells present as very abnormal and grow quickly. This is also known as a high-grade tumour.

Once your tumour has been staged and graded, your doctor may recommend genetic testing, which analyses your tumour DNA and can help determine which treatment has the greatest chance of success. They will then discuss the most appropriate treatment option for you.

Treatment is dependent on several factors, including location, stage of disease and overall health. There is no one treatment option for this type of cancer, due to the rarity of the disease.

Treatment options for non-functional pNETs may include:

  • Surgery, potentially including:
    • Pancreaticoduodenectomy, also known as a Whipple procedure.
    • Distal pancreatectomy.
    • Total pancreatectomy.
  • Radiation therapy, potentially including peptide receptor radionuclide therapy (PRRT).
  • Chemotherapy.
  • Clinical trials.
  • Palliative care.

Risk factors

The risk factors for this disease are the same across all types of pNETs. They include:

  • Family history of cancer.
  • Having conditions such as:
    • Type 2 diabetes.
    • Multiple endocrine neoplasia type 1 (MEN1).
    • Neurofibromatosis type 1 (NFT1).
    • Von Hippel-Lindau (VHL) disease.
    • Tuberous sclerosis
  • Being a smoker or having a history of smoking.
  • Excessive alcohol intake.
  • Obesity.

Not everyone with these risk factors will develop the disease, and some people who have the disease may have none of these risk factors. See your general practitioner (GP) if you are concerned.

Symptoms

Early-stage non-functional pNETs may appear asymptomatic. As the tumour progresses, some of the following symptoms may occur:

  • Diarrhoea.
  • Indigestion.
  • Abdominal and/or back pain.
  • A lump in the abdomen.
  • Jaundice.

Not everyone with the symptoms above will have cancer but see your general practitioner (GP) if you are concerned.

Some of the information regarding symptoms was obtained from the Pancreatic Neuroendocrine Tumors (Islet Cell Tumors) Treatment (PDQ) page published by the National Cancer Institute.

Diagnosis

If your doctor suspects you have a non-functioning pNET, they may order the following tests to confirm the diagnosis and refer you to a specialist for treatment:

  • Physical examination.
  • Endocrine studies.
  • Imaging tests, potentially including:
    • MRI (magnetic resonance imaging).
    • CT (computed tomography) scan.
    • PET (positron emission tomography) scan.
    • Ultrasound.
  • Exploratory surgery.
  • Biopsy.

References

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