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Checking whether early pancreatic cancer screening can work in Swiss family doctor practices

Tests an MRI and blood test pathway in people 60 or older with risk signs.

Plain-language title generated from the registry record
Registry title: Structured Case-Finding for Pancreatic Ductal Adenocarcinoma in Swiss Primary Care: A Feasibility Study

Key facts

Where
Zurich, SwitzerlandSee the site

Where in Switzerland

  • Onkozentrum Zürich AGZurich, SwitzerlandNo longer taking part

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Trial details

Who runs it
Saskia Hendrich
Trial code
NCT07723781
Record updated
23 July 2026
Original description
Pancreatic ductal adenocarcinoma (PDAC) is diagnosed at an advanced, incurable stage in more than 80% of cases in Switzerland. Certain warning signs - new-onset diabetes, unexplained weight loss, or a family history of pancreatic cancer - may indicate elevated risk, but are not systematically assessed in primary care.Read full original descriptionShow less

PANCATCH-Pilot: Structured Early Detection of Pancreatic Ductal Adenocarcinoma in Swiss Primary Care - A Prospective Feasibility Study of a Case-Finding Pathway in the Canton of Zurich

Pancreatic ductal adenocarcinoma (PDAC) is diagnosed at an advanced, incurable stage in more than 80% of cases in Switzerland. Certain warning signs - new-onset diabetes, unexplained weight loss, or a family history of pancreatic cancer - may indicate elevated risk, but are not systematically assessed in primary care.

PANCATCH-Pilot tests whether a structured case-finding pathway in Swiss general practices is feasible. Adults aged 60 years or older with one or more of these risk factors are invited to undergo an MRI/MRCP examination of the pancreas and a blood draw for a blinded biomarker test (PancreaSure, Immunovia Inc.). Findings are reviewed by a multidisciplinary tumour board. The goal is not treatment, but to assess whether such a pathway works in the Swiss primary care context - as preparation for a larger national study.

The study enrolls 50 trigger-positive participants over 24 months through two parallel recruitment pathways: GP referral and self-presentation via a study website. Feasibility is assessed using six combined endpoints covering recruitment, process quality, safety, and equity.

Inclusion: Age 60 years or older; Attendance at a participating GP practice in Canton Zurich or adjacent canton (maximum 1 hour travel time), or self-presentation via study microsite; At least one trigger criterion fulfilled: metabolic trigger (new-onset type 2 diabetes mellitus diagnosed within 24 months AND unintentional weight loss >5% body weight within 3 months) OR familial/genetic trigger (≥2 first-degree relatives with PDAC, or ≥1 first-degree relative with PDAC, or BRCA1/2 germline mutation, or CDKN2A mutation); combined with age ≥60 years; Written informed consent; Sufficient German or English language skills for study communication.

Exclusion: Prior or current diagnosis of pancreatic carcinoma or pre-malignant pancreatic lesion; Contraindication to MRI (metallic implants, severe claustrophobia without available alternative); Active untreated psychiatric condition impairing capacity to consent; Pregnancy; Incapacity to provide informed consent.

ClinicalTrials.gov NCT07723781