What does Pancreatic Cancer Europe do?


Pancreatic Cancer Europe is a European multi-stakeholder platform which aims at bringing together experts from all over Europe including academics, physicians, politicians, patient groups, journalists and industry with a common interest and willingness to improve care for patients with pancreatic cancer.

How we aim to achieve our mission

Pancreatic Cancer Europe aims at bringing together relevant stakeholders to advocate for an improvement in the standard of care for patients with pancreatic cancer, by addressing the existing gaps related to the lack of awareness, diagnosis and data collection. Spun off by a strong political will to address the devastating impact of pancreatic cancer, Pancreatic Cancer Europe aims at reversing the trend of pancreatic cancer impact by:

There are four main work streams:

  1. Awareness and Diagnosis 
  2. Registries
  3. National Support
  4. Research 

PCE has produced several documents and awareness materials including a micro site, symptoms posters, 10 key facts and GP leaflets on diagnosing pancreatic cancer.

Find out more about campaigning in europe.

Awareness Workstream

Pancreatic cancer is often referred to as a “forgotten cancer”. A key goal of the Pancreatic Cancer Europe Awareness Workstream is to ensure that this cancer is not forgotten by policy makers, so that appropriate policies can be implemented.

While it represented 16.8% of the mortality from the deadliest cancers in 2012, pancreatic cancer only represented 3.4% of parliamentary questions on these cancers tabled in the European Parliament between 2009 and 2014.

The outputs for 2015 from the Awareness Workstream

Includes the 10 key facts leaflet and a Pancreatic Cancer Declaration document.  These documents have been translated into 12 languages.

10 things


Download the PDF documents here:

10 things you need to know


10 Warning Signs of pancreatic cancer