Improvement of the quality of BRAF testing in melanomas with nationwide external quality assessment, for the BRAF EQA group

Jean François Emile, Julie Tisserand, Loic Bergougnoux, Frédérique Nowak, Gladwys Faucher, Sylvie Surel, Aude Lamy, Delphine Lecorre, Zofia Helias-Rodzewicz, Paul Hofman, Jean Christophe Sabourin, Pierre Laurent-Puig, Drs Cécile Aube, Lebkir Baala, Jean Ben Hattar, Christophe Boyer, Frédéric Charlotte, Pascale Cervera, Eric Clauser, Florence De FraipontPierre Dechelotte, Chantal Delvincourt, Marc Denis, Laurent Doucet, Karine Durand, Fabienne Escande, Carole Ferraro-Peyret, Françoise Galateau-Salle, Cécile Haratyk, Rémy Heller, Philippe Jonveaux, Lucie Karayan-Tapon, Roger Lacave, Ludovic Lacroix, Laurence Lamant, Jérôme Lamoril, Jean Lamy, Antoinette Lemoine, Karen Leroy, Sarab Lizard, Fernando Lopez-Rios, Sabine Merkelbach-Bruse, Jean Louis Merlin, Jean Philippe Merlio, Samia Mourah, Isabelle Nanni Metellus, Jean Pages, Florence Pedeutour, Michel Peoc'h, Jean Luc Pretet, Delphine Prunier, Nathalie Rioux-Leclercq, Etienne Rouleau, Hagay Sobol, Jérôme Solassol, Stéphanie Trudel, Sabine Vande Borght, Qing Wang

    Résultats de recherche: Contribution à un journalArticleRevue par des pairs

    11 Citations (Scopus)

    Résumé

    Background: Knowledge about tumour gene mutation status is essential for the treatment of increasing numbers of cancer patients, and testing quality has a major impact on treatment response and cost. In 2012, 4,629 tests for BRAF p.V600 were performed in France, in patients with melanomas.Methods: Two batches of unstained melanoma sections were sent, in May and November 2012, to the 46 laboratories supported by the French National Institute of Cancer (INCa). An external quality assessment (EQA) evaluated mutation status, response times and compliance with INCa recommendations.Results: All the French laboratories involved in testing participated in the EQA. Fourteen different methods were used to detect BRAF mutations, most consisting of combinations of in-house techniques. False responses were noted in 25/520 cases (4.8%), 11 of which concerned confusion between p.V600E and p.V600K. Thus, 2.7% of responses would have led to inappropriate treatment. Within six months, mean response times decreased from 22 to 12 days (P<0.001), and the percentage of samples evaluated by a pathologist for tumour cell content increased, from 75.2% to 96.9% (P<0.001).Conclusion: Despite the use of non-certified methods, the false response rate was low. Nationwide EQA can improve the quality of molecular pathology tests on tumours.

    langue originaleAnglais
    Numéro d'article472
    journalBMC Cancer
    Volume13
    Les DOIs
    étatPublié - 11 oct. 2013

    Contient cette citation