{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T15:58:32Z","timestamp":1790351912659,"version":"4.1.0"},"reference-count":28,"publisher":"Wiley","issue":"19","license":[{"start":{"date-parts":[[2024,5,29]],"date-time":"2024-05-29T00:00:00Z","timestamp":1716940800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["acsjournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Cancer"],"published-print":{"date-parts":[[2024,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Pancreatic ductal adenocarcinoma (PDAC) surveillance is recommended for some individuals with a pathogenic or likely pathogenic variant (PV\/LPV) in a PDAC susceptibility gene; the recommendation is often dependent on family history of PDAC. This study aimed to describe PDAC family history in individuals with PDAC who underwent genetic testing to determine the appropriateness of including a family history requirement in these recommendations.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Individuals with PDAC with a germline heterozygous PV\/LPV in <jats:italic>ATM<\/jats:italic>, <jats:italic>BRCA1<\/jats:italic>, <jats:italic>BRCA2<\/jats:italic>, <jats:italic>EPCAM<\/jats:italic>, <jats:italic>MLH1<\/jats:italic>, <jats:italic>MSH2<\/jats:italic>, <jats:italic>MSH6<\/jats:italic>, <jats:italic>PALB2<\/jats:italic>, or <jats:italic>PMS2<\/jats:italic> (PV\/LPV carriers) were assessed for family history of PDAC in first\u2010degree relatives (FDRs) or second\u2010degree relatives (SDRs) from nine institutions. A control group of individuals with PDAC without a germline PV\/LPV was also assessed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The study included 196 PV\/LPV carriers and 1184 controls. In the PV\/LPV carriers, 25.5% had an affected FDR and\/or SDR compared to 16.9% in the control group (<jats:italic>p<\/jats:italic>\u00a0=\u00a0.004). PV\/LPV carriers were more likely to have an affected FDR compared to the controls (<jats:italic>p<\/jats:italic>\u00a0=\u00a0.003) but there was no statistical difference when assessing only affected SDRs (<jats:italic>p<\/jats:italic>\u00a0=\u00a0.344).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Most PV\/LPV carriers who developed PDAC did not have a close family history of PDAC and would not have met most current professional societies\u2019 recommendations for consideration of PDAC surveillance before diagnosis. However, PV\/LPV carriers were significantly more likely to have a family history of PDAC, particularly an affected FDR. These findings support family history as a risk modifier in PV\/LPV carriers, and highlight the need to identify other risk factors.<\/jats:p><\/jats:sec>","DOI":"10.1002\/cncr.35383","type":"journal-article","created":{"date-parts":[[2024,5,29]],"date-time":"2024-05-29T11:26:18Z","timestamp":1716981978000},"page":"3297-3304","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["The role of family history in predicting germline pathogenic variant carriers who develop pancreatic cancer: Results of a multicenter collaboration"],"prefix":"10.1002","volume":"130","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2916-0425","authenticated-orcid":false,"given":"Eve","family":"Karloski","sequence":"first","affiliation":[{"name":"Department of Medicine University of Pittsburgh  Pittsburgh Pennsylvania 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