Diagnostics (Feb 2023)

An Italian Multicenter Perspective Harmonization Trial for the Assessment of MET Exon 14 Skipping Mutations in Standard Reference Samples

  • Paolo Bironzo,
  • Francesco Pepe,
  • Gianluca Russo,
  • Pasquale Pisapia,
  • Gianluca Gragnano,
  • Gabriella Aquino,
  • Silvia Bessi,
  • Simonetta Buglioni,
  • Federico Bartoccini,
  • Giuseppina Ferrero,
  • Michela Anna Bresciani,
  • Paola Francia di Celle,
  • Francesca Sibona,
  • Andrea Giusti,
  • Alessandra Movilia,
  • Renata Mariella Farioli,
  • Alessandra Santoro,
  • Domenico Salemi,
  • Stefania Scarpino,
  • Dino Galafate,
  • Stefania Tommasi,
  • Rosanna Lacalamita,
  • Davide Seminati,
  • Elham Sajjadi,
  • Silvia Novello,
  • Fabio Pagni,
  • Giancarlo Troncone,
  • Umberto Malapelle

DOI
https://doi.org/10.3390/diagnostics13040629
Journal volume & issue
Vol. 13, no. 4
p. 629

Abstract

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Lung cancer remains the leading cause of cancer deaths worldwide. International societies have promoted the molecular analysis of MET proto-oncogene, receptor tyrosine kinase (MET) exon 14 skipping for the clinical stratification of non-small cell lung cancer (NSCLC) patients. Different technical approaches are available to detect MET exon 14 skipping in routine practice. Here, the technical performance and reproducibility of testing strategies for MET exon 14 skipping carried out in various centers were evaluated. In this retrospective study, each institution received a set (n = 10) of a customized artificial formalin-fixed paraffin-embedded (FFPE) cell line (Custom METex14 skipping FFPE block) that harbored the MET exon 14 skipping mutation (Seracare Life Sciences, Milford, MA, USA), which was previously validated by the Predictive Molecular Pathology Laboratory at the University of Naples Federico II. Each participating institution managed the reference slides according to their internal routine workflow. MET exon 14 skipping was successfully detected by all participating institutions. Molecular analysis highlighted a median Cq cut off of 29.3 (ranging from 27.1 to 30.7) and 2514 (ranging from 160 to 7526) read counts for real-time polymerase chain reaction (RT-PCR) and NGS-based analyses, respectively. Artificial reference slides were a valid tool to harmonize technical workflows in the evaluation of MET exon 14 skipping molecular alterations in routine practice.

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