Survival for somatostatinoma

Somatostatinoma is a type of neuroendocrine tumour (NET) that usually starts in the pancreas or small bowel. Survival for somatostatinomas depends on many factors. So no one can tell you exactly how long you will live.

Doctors usually work out the outlook for a certain disease by looking at large groups of people. Because somatostatinomas are rare cancers, the survival of this disease is harder to estimate than for other, more common cancers.

These are general statistics based on small groups of people. Remember, they can’t tell you what will happen in your individual case. Your doctor can give you more information about your own outlook (prognosis).

You can also talk about this with the Cancer Research UK nurses on freephone 0808 800 4040, from 9am to 5pm, Monday to Friday.

About these statistics

The terms 1 year, 5 year and 10 year survival don't mean that you will only live for 1, 5 or 10 years.

The Office for National Statistics (ONS) and researchers collect information. They watch what happens to people with cancer in the years after their diagnosis. 5 or 10 years is a common time point to measure survival. But some people live much longer than this.

5 or 10 year survival is the number of people who have not died from their cancer within 5 or 10 years after diagnosis.

Survival for somatostatinomas

There are no UK survival statistics for all the different types of NETs. The statistics below come from an international study. Please be aware that due to differences in health care systems, data collection and the population, these figures may not be a true picture of survival in the UK.

Most people with a somatostatinoma that hasn't spread to other parts of the body have surgery to try to cure their cancer.

Almost 80 out of every 100 people (almost 80%) survive somatostatinomas for 5 years or more after having surgery to try to cure their cancer.

Survival for NETs of the pancreas

1 year survival

The information below is for 1 year overall survival for pancreatic neuroendocrine neoplasms (NENs) in the UK.

Around 80 in 100 people (around 80%) survive for 1 year or more.

5 year survival

There are no UK-wide 5 year survival statistics available for pancreatic NENs. The statistics below are from a European study. Please be aware that these figures may not be a true picture of survival in the UK. This is due to differences in health care systems, data collection and the population,

Around 40 out of 100 people (around 40%) survive their cancer for 5 years or more after diagnosis.

What affects survival

Survival depends on many factors. It depends on the stage and grade of the tumour when it was diagnosed. The stage describes the size of the tumour and whether it has spread. The grade means how abnormal the cells look under a microscope.

Another factor is how well you are overall. 

What next?

You might want to read our information about treatment for somatostatinomas. 

This page is due for review. We will update this as soon as possible.

  • Pancreatic neuroendocrine tumors (PNETs): incidence, prognosis and recent trend toward improved survival 
    T Halfdanarson and others
    Annals of Oncology, 2008. Vol 19, Pages 1727-1733

  • Impact of neuroendocrine morphology on cancer outcomes and stage at diagnosis: a UK nationwide cohort study 2013–2015
    T Genus and others
    British Journal of Cancer (2019) Volume 121, pages 966–972

     

  • Somatostatinoma syndrome
    P Economopoulos and C Christopoulos
    Annals of Gastroenterology, 2001. Vol 14, Issue 4, Pages 252-260

  • Rare functioning pancreatic endocrine tumors
    D O'Toole and others
    Neuroendocrinology, 2006. Vol 84, Pages 189-195

  • ENETS consensus guidelines for the management of patients with digestive neuroendocrine neoplasms: functional pancreatic endocrine tumor syndromes 
    R T Jensen and others
    Neuroendocrinology, 2012. Vol 95, Pages 98-119 

  • Rare neuroendocrine tumours: Results of the surveillance of rare cancers in Europe project
    J Maartaen Van de Zwan and others
    European Journal of Cancer, 2013. Volume 49, Issue 11, Pages 2565-2578

Last reviewed: 
24 Jun 2022
Next review due: 
24 Jun 2025

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