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. Author manuscript; available in PMC: 2020 Jun 15.
Published in final edited form as: Gut. 2019 Oct 31;69(1):7–17. doi: 10.1136/gutjnl-2019-319352

Table 3.

Summary of the main recommendations of the 2019 International Cancer of the Pancreas Surveillance (CAPS) Consortium

Who?

► All patients with Peutz-Jeghers syndrome (carriers of a germline LKB1/STK11 gene mutation)
► All carriers of a germline CDKN2A mutation
► Carriers of a germline BRCA2, BRCA1, PALB2, ATM, MLH1, MSH2, or MSH6 gene mutation with at least one affected first-degree blood relative
► Individuals who have at least one first-degree relative with pancreatic cancer who in turn also has a first-degree relative with pancreatic cancer (familial pancreatic cancer kindred)
When (at what age)?
► Age to initiate surveillance depends on an individual's gene mutation status and family history
Familial pancreatic cancer kindred (without a known germline mutation) Start at age 50 or 55* or 10 years younger than the youngest affected blood relative
Mutation carriers: For CDKN2A, Peutz-Jegher syndrome, start at age 40; BRCA2,ATM, PALB2 BRCA1, MLH1/MSH2 start at age 45 or 50 or 10 years younger than youngest affected blood relative
► There is no consensus on the age to end surveillance
How?
At baseline ► MRI/MRCP+EUS + fasting blood glucose and/or HbAlc
During follow-up ► Alternate MRI/MRCP and EUS (no consensus if and how to alternate)
► Routinely test fasting blood glucose and/or HbA1c
On indication ► Serum CA 19–9 ► If concerning features on imaging
► EUS-FNA only for ► Solid lesions of ≥5 mm
► Cystic lesions with worrisome features
► Asymptomatic MPD strictures (with or without mass)
► CT only ► Solid lesions, regardless o
► Asymptomatic MPD strictures of unknown aetiology (without mass)
Intervals and surgery
12 Months ► If no abnormalities, or only non-concerning abnormalities (eg, pancreatic cysts without worrisome features)
3 or 6 Months ► If concerning abnormalities for which immediate surgery is not indicated (see figure 2 for details)
Surgery ► If positive FNA and/or a high suspicion of malignancy on imaging (see figure 2 for details)
► When surgery is indicated, perform an oncological radical resection at a specialty centre
Goals
The goal of surveillance is to detect and treat the following pathological lesions ► Stage I pancreatic cancer, confined to the pancreas, resected with negative margins
► Pancreatic cancer precursor lesions with high-grade dysplasia (PanIN or IPMN)
*

Consensus as to when to start surveillance was not reached.

Literature-based recommendation.

ATM, ataxia telangiectasia mutated; BRCA2, breast cancer 2; CDKN2A, cyclin-dependent kinase inhibitor 2A; CT, computed tomography; EUS, endoscopic ultrasound; FNA, fine-needle aspiration; HbA1c, hemoglobin A1c; IPMN, intraductal papillary mucinous neoplasm; MLH1, mutL homolog 1; MPD, main pancreatic duct; MRI/MRCP, magnetic resonance imaging/magnetic retrograde cholangiopancreatography; MSH2, mutS homolog 2; MSH6, mutS homolog 6; PALB2, partner and localizer of BRCA2; PanIN, pancreatic intraepithelial neoplasia; STK11, serine/ threonine kinase 11.