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Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations

Pascal Pujol 1 Pierre Vande Perre Laurence Faivre 2, 3, 4, 5 Damien Sanlaville 6 Carole Corsini 7 Bernard Baertschi 8 Michèle Anahory Dominique Vaur 9 Sylviane Olschwang 10 Nadem Soufir 11 Noëlle Bastide Sarah Amar 12 Michèle Vintraud Olivier Ingster 13 Stéphane Richard Pierre Le Coz 14 Jean-Philippe Spano 15 Olivier Caron 16 Pascal Hammel 17 Elisabeth Luporsi 18 Alain Toledano 19 Xavier Rebillard 20 Anne Cambon-Thomsen 21 Olivier Putois 22 Jean-Marc Rey 7 Christian Hervé 23, 24 Caroline Zorn Karen Baudry 7 Virginie Galibert 7 Joseph Gligorov 25 David Azria 26, 27 Brigitte Bressac-de Paillerets 28 Nelly Burnichon 29 Marc Spielmann 30 Daniel Zarca Isabelle Coupier 7 Olivier Cussenot 31 Anne-Paule Gimenez-Roqueplo 32, 24 Sophie Giraud 33 Anne-Sophie Lapointe 23, 24 Patricia Niccoli 34 Isabelle Raingeard 35 Muriel Le Bidan Thierry Frébourg 36 Arash Rafii 37 David Geneviève 38, 39
28 Génétique (Biologie pathologie)
Département de biologie et pathologie médicales [Gustave Roussy]
Abstract : In oncology, the expanding use of multi-gene panels to explore familial cancer predisposition and tumor genome analysis has led to increased secondary findings discoveries (SFs) and has given rise to important medical, ethical, and legal issues. The American College of Medical Genetics and Genomics published a policy statement for managing SFs for a list of genes, including 25 cancer-related genes. Currently, there are few recommendations in Europe. From June 2016 to May 2017, the French Society of Predictive and Personalized Medicine (SFMPP) established a working group of 47 experts to elaborate guidelines for managing information given on the SFs for genes related to cancers. A subgroup of ethicists, lawyers, patients’ representatives, and psychologists provided ethical reflection, information guidelines, and materials (written consent form and video). A subgroup with medical expertise, including oncologists and clinical and molecular geneticists, provided independent evaluation and classification of 60 genes. The main criteria were the “actionability” of the genes (available screening or prevention strategies), the risk evaluation (severity, penetrance, and age of disease onset), and the level of evidence from published data. Genes were divided into three classes: for class 1 genes (n = 36), delivering the information on SFs was recommended; for class 2 genes (n = 5), delivering the information remained questionable because of insufficient data from the literature and/or level of evidence; and for class 3 genes (n = 19), delivering the information on SFs was not recommended. These guidelines for managing SFs for cancer-predisposing genes provide new insights for clinicians and laboratories to standardize clinical practices.
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Soumis le : vendredi 7 septembre 2018 - 14:38:50
Dernière modification le : samedi 20 novembre 2021 - 12:02:01

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Pascal Pujol, Pierre Vande Perre, Laurence Faivre, Damien Sanlaville, Carole Corsini, et al.. Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations. European Journal of Human Genetics, Nature Publishing Group, 2018, 26 (12), pp.1732-1742. ⟨10.1038/s41431-018-0224-1⟩. ⟨hal-01870352⟩



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