Assessment of major gaps from the perspective of patients, patient advocates and NET health care professionals.
Due to the increasing incidence and prevalence of neuroendocrine tumors (NETs), there is a need to assess any gaps in awareness and care. A survey was undertaken in 2017 to identify perceived unmet needs from the perspectives of patients/families, patient advocates and health care professionals (HCPs). The survey consisted of 33–37 questions (depending on type of respondent) across four areas: information, care, treatments and research.
Recent News
NEW PODCAST – Neuroendocrine Cancer and Quality of Life Research: Conversations with Prof. John Ramage
We are excited to present our latest podcast episode, where we delve into the intriguing world of quality-of-life research with a distinguished expert in the field, Professor John Ramage. Prof. Ramage is a consultant physician specialising in gastroenterology and...
New Podcast: Beyond the Lab: Unravelling Rare Cancer with Andy Hall
Neuroendocrine Cancer UK is excited to announce the newest episode in our Not Just NE Cancer Takeover Podcast Series. This episode delves into the realm of research, featuring an interview with Andy Hall, the Chief Scientific Officer at RareCan - an organisation...
INCA Monthly Newsletter Highlights July 2023
We are delighted to share highlights from the latest newsletter from INCA (International Neuroendocrine Cancer Alliance) - please note that while some initiatives may be country/region specific, there are parallels: similarities, and differences, that resonate across...