The detailed manuscript on titled “Patient-Reported Experience of Diagnosis, Management, and Burden of Neuroendocrine Tumors: Results from a Large Patient Survey in the United States,” is now available for viewing.
The aim of this survey was to examine the experience of patients with NETs to raise awareness of the NET-related burden and identify unmet needs. This manuscript reports on data from patients in the United States.
Check it out here: Patient Survey – Pancreas Journal
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Shaping the future of cancer control together We are pleased to send you this update on the Australian Cancer Plan, the first national 10-year
Recruiting NET health professionals for International Delphi survey Development of a neuroendocrine tumour (NET) nutrition-risk screening tool to identify patients requiring nutrition intervention and education
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