Literature DB >> 30731170

Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT.

Nicholas J Taylor1, Nandita Mitra2, Lu Qian3, Marie-Françoise Avril4, D Timothy Bishop5, Brigitte Bressac-de Paillerets6, William Bruno7, Donato Calista8, Francisco Cuellar9, Anne E Cust10, Florence Demenais11, David E Elder12, Anne-Marie Gerdes13, Paola Ghiorzo7, Alisa M Goldstein14, Thais C Grazziotin15, Nelleke A Gruis16, Johan Hansson17, Mark Harland5, Nicholas K Hayward18, Marko Hocevar19, Veronica Höiom17, Elizabeth A Holland20, Christian Ingvar21, Maria Teresa Landi14, Gilles Landman22, Alejandra Larre-Borges23, Graham J Mann20, Eduardo Nagore24, Håkan Olsson21, Jane M Palmer18, Barbara Perić19, Dace Pjanova25, Antonia L Pritchard18, Susana Puig26, Helen Schmid20, Nienke van der Stoep27, Margaret A Tucker14, Karin A W Wadt13, Xiaohong R Yang14, Julia A Newton-Bishop5, Peter A Kanetsky28.   

Abstract

BACKGROUND: Although rare in the general population, highly penetrant germline mutations in CDKN2A are responsible for 5%-40% of melanoma cases reported in melanoma-prone families. We sought to determine whether MELPREDICT was generalizable to a global series of families with melanoma and whether performance improvements can be achieved.
METHODS: In total, 2116 familial melanoma cases were ascertained by the international GenoMEL Consortium. We recapitulated the MELPREDICT model within our data (GenoMELPREDICT) to assess performance improvements by adding phenotypic risk factors and history of pancreatic cancer. We report areas under the curve (AUC) with 95% confidence intervals (CIs) along with net reclassification indices (NRIs) as performance metrics.
RESULTS: MELPREDICT performed well (AUC 0.752, 95% CI 0.730-0.775), and GenoMELPREDICT performance was similar (AUC 0.748, 95% CI 0.726-0.771). Adding a reported history of pancreatic cancer yielded discriminatory improvement (P < .0001) in GenoMELPREDICT (AUC 0.772, 95% CI 0.750-0.793, NRI 0.40). Including phenotypic risk factors did not improve performance.
CONCLUSION: The MELPREDICT model functioned well in a global data set of familial melanoma cases. Adding pancreatic cancer history improved model prediction. GenoMELPREDICT is a simple tool for predicting CDKN2A mutational status among melanoma patients from melanoma-prone families and can aid in directing these patients to receive genetic testing or cancer risk counseling.
Copyright © 2019 American Academy of Dermatology, Inc. All rights reserved.

Entities:  

Keywords:  CDKN2A; GenoMEL; GenoMELPREDICT; familial melanoma; mutation prediction

Mesh:

Substances:

Year:  2019        PMID: 30731170      PMCID: PMC6634996          DOI: 10.1016/j.jaad.2019.01.079

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  25 in total

Review 1.  Genetic epidemiology of cutaneous melanoma: a global perspective.

Authors:  A M Goldstein; M A Tucker
Journal:  Arch Dermatol       Date:  2001-11

Review 2.  Counseling and DNA testing for individuals perceived to be genetically predisposed to melanoma: A consensus statement of the Melanoma Genetics Consortium.

Authors:  R F Kefford; J A Newton Bishop; W Bergman; M A Tucker
Journal:  J Clin Oncol       Date:  1999-10       Impact factor: 44.544

3.  Population-based analysis of prognostic factors and survival in familial melanoma.

Authors:  Scott R Florell; Kenneth M Boucher; Gilda Garibotti; John Astle; Richard Kerber; Geraldine Mineau; Charles Wiggins; R Dirk Noyes; Alexander Tsodikov; Lisa A Cannon-Albright; John J Zone; Wolfram E Samlowski; Sancy A Leachman
Journal:  J Clin Oncol       Date:  2005-10-01       Impact factor: 44.544

4.  MELPREDICT: a logistic regression model to estimate CDKN2A carrier probability.

Authors:  K B Niendorf; W Goggins; G Yang; K Y Tsai; M Shennan; D W Bell; A J Sober; D Hogg; H Tsao
Journal:  J Med Genet       Date:  2005-09-16       Impact factor: 6.318

5.  Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.

Authors:  Alisa M Goldstein; May Chan; Mark Harland; Nicholas K Hayward; Florence Demenais; D Timothy Bishop; Esther Azizi; Wilma Bergman; Giovanna Bianchi-Scarra; William Bruno; Donato Calista; Lisa A Cannon Albright; Valerie Chaudru; Agnes Chompret; Francisco Cuellar; David E Elder; Paola Ghiorzo; Elizabeth M Gillanders; Nelleke A Gruis; Johan Hansson; David Hogg; Elizabeth A Holland; Peter A Kanetsky; Richard F Kefford; Maria Teresa Landi; Julie Lang; Sancy A Leachman; Rona M MacKie; Veronica Magnusson; Graham J Mann; Julia Newton Bishop; Jane M Palmer; Susana Puig; Joan A Puig-Butille; Mitchell Stark; Hensin Tsao; Margaret A Tucker; Linda Whitaker; Emanuel Yakobson
Journal:  J Med Genet       Date:  2006-08-11       Impact factor: 6.318

6.  Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample.

Authors:  Colin B Begg; Irene Orlow; Amanda J Hummer; Bruce K Armstrong; Anne Kricker; Loraine D Marrett; Robert C Millikan; Stephen B Gruber; Hoda Anton-Culver; Roberto Zanetti; Richard P Gallagher; Terence Dwyer; Timothy R Rebbeck; Nandita Mitra; Klaus Busam; Lynn From; Marianne Berwick
Journal:  J Natl Cancer Inst       Date:  2005-10-19       Impact factor: 13.506

7.  Geographical variation in the penetrance of CDKN2A mutations for melanoma.

Authors:  D Timothy Bishop; Florence Demenais; Alisa M Goldstein; Wilma Bergman; Julia Newton Bishop; Brigitte Bressac-de Paillerets; Agnès Chompret; Paola Ghiorzo; Nelleke Gruis; Johan Hansson; Mark Harland; Nicholas Hayward; Elizabeth A Holland; Graham J Mann; Michela Mantelli; Derek Nancarrow; Anton Platz; Margaret A Tucker
Journal:  J Natl Cancer Inst       Date:  2002-06-19       Impact factor: 13.506

Review 8.  Selection criteria for genetic assessment of patients with familial melanoma.

Authors:  Sancy A Leachman; John Carucci; Wendy Kohlmann; Kimberly C Banks; Maryam M Asgari; Wilma Bergman; Giovanna Bianchi-Scarrà; Teresa Brentnall; Brigitte Bressac-de Paillerets; William Bruno; Clara Curiel-Lewandrowski; Femke A de Snoo; Tadeusz Debniak; Marie-France Demierre; David Elder; Alisa M Goldstein; Jane Grant-Kels; Allan C Halpern; Christian Ingvar; Richard F Kefford; Julie Lang; Rona M MacKie; Graham J Mann; Kurt Mueller; Julia Newton-Bishop; Håkan Olsson; Gloria M Petersen; Susana Puig; Darrell Rigel; Susan M Swetter; Margaret A Tucker; Emanuel Yakobson; John A Zitelli; Hensin Tsao
Journal:  J Am Acad Dermatol       Date:  2009-10       Impact factor: 11.527

9.  Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of LAMBDA, BRCAPRO, Myriad II, and modified Couch models.

Authors:  Noralane M Lindor; Rachel A Lindor; Carmel Apicella; James G Dowty; Amanda Ashley; Katherine Hunt; Betty A Mincey; Marcia Wilson; M Cathie Smith; John L Hopper
Journal:  Fam Cancer       Date:  2007-07-17       Impact factor: 2.375

10.  A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL).

Authors:  Mark Harland; Alisa M Goldstein; Kairen Kukalizch; Claire Taylor; David Hogg; Susana Puig; Celia Badenas; Nelleke Gruis; Jeanet ter Huurne; Wilma Bergman; Nicholas K Hayward; Mitchell Stark; Hensin Tsao; Margaret A Tucker; Maria Teresa Landi; Giovanna Bianchi Scarra; Paola Ghiorzo; Peter A Kanetsky; David Elder; Graham J Mann; Elizabeth A Holland; D Timothy Bishop; Julia Newton Bishop
Journal:  Eur J Cancer       Date:  2008-04-03       Impact factor: 9.162

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Journal:  Cells       Date:  2019-06-04       Impact factor: 6.600

2.  Predictors of germline status for hereditary melanoma: 5 years of multi-gene panel testing within the Italian Melanoma Intergroup.

Authors:  W Bruno; B Dalmasso; M Barile; V Andreotti; L Elefanti; M Colombino; I Vanni; E Allavena; F Barbero; E Passoni; B Merelli; S Pellegrini; F Morgese; R Danesi; V Calò; V Bazan; A V D'Elia; C Molica; F Gensini; E Sala; V Uliana; P F Soma; M Genuardi; A Ballestrero; F Spagnolo; E Tanda; P Queirolo; M Mandalà; I Stanganelli; G Palmieri; C Menin; L Pastorino; P Ghiorzo
Journal:  ESMO Open       Date:  2022-06-28

Review 3.  Genetic risk factors in melanoma etiopathogenesis and the role of genetic counseling: A concise review.

Authors:  Nikola Serman; Semir Vranic; Mislav Glibo; Ljiljana Serman; Zrinka Bukvic Mokos
Journal:  Bosn J Basic Med Sci       Date:  2022-09-16       Impact factor: 3.759

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