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Harmonization of Reporting of ALK Genetic Alterations in Neuroblastoma: A SIOPEN Biology Study

  • Alexandra Saint-Charles
  • , Julien Masliah-Planchon
  • , Elnaz Saberi-Ansari
  • , Angela Bellini
  • , Marie Bernkopf
  • , Jaime Font de Mora
  • , Rosa Noguera
  • , Nadine Van Roy
  • , Angharad Goodman
  • , Ales Vicha
  • , Valery Attignon
  • , Valérie Combaret
  • , Klaus Beiske
  • , Tommy Martinsson
  • , Jacqueline Schoumans
  • , Maria Rossing
  • , Bastiaan Tops
  • , Frank Westermann
  • , Sophie Cotteret
  • , Matthias Fischer
  • Yehudit Birger, Katia Mazzocco, Louis Chesler, David Betts, Mark Cowley, Mario Capasso, Charles Bobin, Yasmine Iddir, Sakina Zaidi, Angel M. Carcaboso, Joni Vandermeulen, Siebe Loontiens, Jennie Gaarder, Raghda R. Ibrahim, Carolina Rosswog, Michal Hameiri-Grossman, Keren Shichrur, Toby Trahair, Paulette Barahona, Angelika Eggert, Hedwig E. Deubzer, Olivier Delattre, Claudia Pasqualini, Sally George, Godelieve Tytgat, Deborah A. Tweddle, Sabine Taschner-Mandl, Gudrun Schleiermacher

Research output: Contribution to journalArticlepeer-review

Abstract

In high-risk neuroblastoma, identification of ALK activating genetic alterations is considered for clinical decision-making at relapse or more recently in frontline treatment. The accurate diagnosis of genetic alterations requires harmonization of molecular techniques and reporting, especially when these concern inclusion criteria for clinical trials. Analysis and validation of 14 DNA samples harboring distinct ALK alterations were performed across the 21 SIOPEN (International Society of Paediatric Oncology Europe Neuroblastoma) molecular diagnostic laboratories. These included ALK mutations at or outside hotspots in the tyrosine kinase domain with variant allele frequencies (VAFs) of 1% to 91% or ALK genomic amplification. Each laboratory used their own techniques: ALK amplifications were detected by pan-genomic copy number techniques or fluorescence in situ hybridization, and ALK mutations were characterized by next-generation sequencing techniques. All laboratories correctly identified high-level ALK amplification and ALK mutations within the known hotspots with VAF >5%, with the exception of two cases. Differences in interpretation and reporting were apparent for samples harboring mutations with a VAF <5% or outside known hotspots. These results highlight the importance of standard operating procedures, standardized reporting, and the robustness of ALK genetic testing in the SIOPEN laboratories, and the need for expert discussions regarding atypical ALK alterations, to validate eligibility for ALK targeted treatment in clinical trials.

Original languageEnglish
Pages (from-to)27-38
Number of pages12
JournalJournal of Molecular Diagnostics
Volume28
Issue number1
DOIs
Publication statusPublished - Jan 2026

Keywords

  • Gene Amplification
  • Neuroblastoma/genetics
  • Humans
  • Gene Frequency
  • Genetic Testing/standards
  • In Situ Hybridization, Fluorescence
  • Anaplastic Lymphoma Kinase/genetics
  • High-Throughput Nucleotide Sequencing
  • Mutation

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