LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patients Journal Articles uri icon

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abstract

  • Abstract Background The international, multicenter registry LOGGIC Core BioClinical Data Bank aims to enhance the understanding of tumor biology in pediatric low-grade glioma (pLGG) and provide clinical and molecular data to support treatment decisions and interventional trial participation. Hence, the question arises whether implementation of RNA sequencing (RNA-Seq) using fresh frozen (FrFr) tumor tissue in addition to gene panel and DNA methylation analysis improves diagnostic accuracy and provides additional clinical benefit. Methods Analysis of patients aged 0 to 21 years, enrolled in Germany between April 2019 and February 2021, and for whom FrFr tissue was available. Central reference histopathology, immunohistochemistry, 850k DNA methylation analysis, gene panel sequencing, and RNA-Seq were performed. Results FrFr tissue was available in 178/379 enrolled cases. RNA-Seq was performed on 125 of these samples. We confirmed KIAA1549::BRAF-fusion (n = 71), BRAF V600E-mutation (n = 12), and alterations in FGFR1 (n = 14) as the most frequent alterations, among other common molecular drivers (n = 12). N = 16 cases (13%) presented rare gene fusions (eg, TPM3::NTRK1, EWSR1::VGLL1, SH3PXD2A::HTRA1, PDGFB::LRP1, GOPC::ROS1). In n = 27 cases (22%), RNA-Seq detected a driver alteration not otherwise identified (22/27 actionable). The rate of driver alteration detection was hereby increased from 75% to 97%. Furthermore, FGFR1 internal tandem duplications (n = 6) were only detected by RNA-Seq using current bioinformatics pipelines, leading to a change in analysis protocols. Conclusions The addition of RNA-Seq to current diagnostic methods improves diagnostic accuracy, making precision oncology treatments (MEKi/RAFi/ERKi/NTRKi/FGFRi/ROSi) more accessible. We propose to include RNA-Seq as part of routine diagnostics for all pLGG patients, especially when no common pLGG alteration was identified.

authors

  • Hardin, Emily C
  • Schmid, Simone
  • Sommerkamp, Alexander
  • Bodden, Carina
  • Heipertz, Anna-Elisa
  • Sievers, Philipp
  • Wittmann, Andrea
  • Milde, Till
  • Pfister, Stefan M
  • von Deimling, Andreas
  • Horn, Svea
  • Herz, Nina A
  • Simon, Michèle
  • Perera, Ashwyn A
  • Azizi, Amedeo
  • Cruz, Ofelia
  • Curry, Sarah
  • Van Damme, An
  • Garami, Miklos
  • Hargrave, Darren
  • Kattamis, Antonis
  • Kotnik, Barbara Faganel
  • Lähteenmäki, Päivi
  • Scheinemann, Katrin
  • Schouten-van Meeteren, Antoinette YN
  • Sehested, Astrid
  • Viscardi, Elisabetta
  • Wormdal, Ole Mikal
  • Zapotocky, Michal
  • Ziegler, David S
  • Koch, Arend
  • Hernáiz Driever, Pablo
  • Witt, Olaf
  • Capper, David
  • Sahm, Felix
  • Jones, David TW
  • van Tilburg, Cornelis M

publication date

  • November 2, 2023