Publications by authors named "S J Deharvengt"

Article Synopsis
  • * A pilot program was launched where pharmacists reviewed genetic test results, provided drug-dosing advice, and documented interactions in patient records, which were shared with oncologists.
  • * Results showed that out of 71 patients, 21 had actionable genetic variants, leading to dose changes in five patients, demonstrating the potential of pharmacist involvement in personalized medicine.
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Molecular analysis plays a growing role in the diagnosis of mesenchymal neoplasms. The aim of this study was to retrospectively apply broad, multiplex molecular assays (a solid tumor targeted next-generation sequencing [NGS]) assay and single nucleotide polymorphism [SNP] microarray) to selected tumors, exploring the current utility and limitations. We searched our database (2010-2020) for diagnostically challenging mesenchymal neoplasms.

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Article Synopsis
  • Scientists studied gliomas, which are types of brain tumors, to see how changes in genes can affect how long patients live and how likely their cancer is to come back.
  • They looked at tissue samples from 293 patients to find specific gene mutations and other changes that might predict patient outcomes.
  • The findings showed that some gene mutations, like IDH1 and MGMT, were linked to better survival rates, while others, like FLT3 and TP53, were linked to worse outcomes.
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Introduction: Activating mutations in the tyrosine kinase domain of the epidermal growth factor receptor () gene in non-small cell lung cancer (NSCLC) patients predicts response to EGFR tyrosine kinase inhibitors (TKIs). The Idylla™ system (Biocartis, Mechelen, Belgium) is a fully integrated, cartridge-based platform that provides automated sample processing and real-time PCR-based mutation detection in a single-use cartridge. This study evaluated the Idylla™ EGFR Mutation Assay cartridges against next-generation sequencing (NGS) using formalin fixed, paraffin embedded (FFPE) lung cancer tissue samples.

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