Design and analytical validation of Nexthyro 2.0, a custom next-generation sequencing panel integrating DNA mutation profiling and RNA fusion detection for routine thyroid pathology specimens
Abstract
Abstract The increasing role of molecular testing in thyroid pathology, from the pre-operative stratification of indeterminate fine-needle aspiration (FNA) categories to the management of advanced carcinomas, has prompted the development of institution-specific custom NGS solutions as a locally deployable alternative to centralized tests. The aim of the present study is to validate a new custom NGS panel dedicated to the molecular analysis of routine thyroid pathology specimens. The panel was evaluated on thyroid cancer cell lines, 124 FFPE thyroid tissue specimens, and 43 FNA samples. Nexthyro 2.0 achieved a high sequencing success rate on both histological (100%) and cytological (95.3%) material, with analytical sensitivity down to 0.5% dilution point. Mutational profiles across thyroid neoplasm histotypes and FNA categories were consistent with established molecular-morphological correlates. Nexthyro 2.0 represents a reliable local solution for thyroid molecular testing across cytological and histological specimens encountered in routine clinical practice.
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Authors: Mariantonia Nacchio, Anna Maria Carillo, Domenica Di Giovanni, Geneviève Belleannée, Beatrix Cochand-Priollet, Myriam Decaussin‐Petrucci, Gabrielle Deniziaut, Hélène Trouette, Philippe Vielh, Elena Vigliar, Umberto Malapelle, Giancarlo Troncone, Claudio Bellevicine
Institutions: Sorbonne Université, Université de Bordeaux, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Federico II University Hospital, Lyon 1 Université, University of Naples Federico II, Université Sorbonne Nouvelle, Bordeaux Population Health, Hôpital Cochin, Hôpital Cardiologique du Haut-Lévêque, Hôpital Lyon Sud, Hôpital américain de paris