Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants. Issue 4 (1st June 2020)

• Record Type: Journal Article
• Authors: Overbeek, Kasper A; Rodríguez-Girondo, Mar DM; Wagner, Anja; van der Stoep, Nienke; van den Akker, Peter C; Oosterwijk, Jan C; van Os, Theo A; van der Kolk, Lizet E; Vasen, Hans F A; Hes, Frederik J; Cahen, Djuna L; Bruno, Marco J; Potjer, Thomas P
• Is Part Of: Journal of medical genetics. Volume 58:Issue 4(2021)
• Page Start: 264
• Page End: 269
• Publication Date: 2020-06-01
• Subjects: clinical genetics -- gastroenterology -- genetic screening/counselling -- pancreas and biliary tract -- oncology; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmedgenet-2019-106562
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : Background: Pathogenic variants in the CDKN2A gene are generally associated with the development of melanoma and pancreatic ductal adenocarcinoma (PDAC), but specific genotype-phenotype correlations might exist and the extent of PDAC risk is not well established for many variants. Methods: Using the Dutch national familial melanoma database, we identified all families with a pathogenic CDKN2A variant and investigated the occurrence of PDAC within these families. We also estimated the standardised incidence ratio and lifetime PDAC risk for carriers of a highly prevalent variant in these families. Results: We identified 172 families in which 649 individuals carried 15 different pathogenic variants. The most prevalent variant was the founder mutation c.225_243del (p16- Leiden, 484 proven carriers). Second most prevalent was c.67G>C (55 proven carriers). PDAC developed in 95 of 163 families (58%, including 373 of 629 proven carriers) harbouring a variant with an effect on the p16INK4a protein, whereas PDAC did not occur in the 9 families (20 proven carriers) with a variant affecting only p14ARF. In the c.67G>C families, PDAC occurred in 12 of the 251 (5%) persons at risk. The standardised incidence ratio was 19.1 (95% CI 8.3 to 33.6) and the cumulative PDAC incidence at age 75 years (lifetime risk) was 19% (95% CI 7.5% to 30.1%). Conclusions: Our results support the notion that pathogenic CDKN2A variants affecting the p16INK4a protein, including c.67G>C, are associated with increased PDAC risk and carriers of such variants should be offered pancreatic cancer surveillance. There is no clinical evidence that impairment of only the p14ARF protein leads to an increased PDAC risk.