Molecular Oncology (Jan 2021)

Fine‐needle aspiration as an alternative to core needle biopsy for tumour molecular profiling in precision oncology: prospective comparative study of next‐generation sequencing in cancer patients included in the SHIVA02 trial

  • Célia Dupain,
  • Julien Masliah‐Planchon,
  • Céline Gu,
  • Elodie Girard,
  • Pierre Gestraud,
  • Pauline Du Rusquec,
  • Edith Borcoman,
  • Diana Bello,
  • Francesco Ricci,
  • Ségolène Hescot,
  • Marie‐Paule Sablin,
  • Patricia Tresca,
  • Alexandre deMoura,
  • Delphine Loirat,
  • Maxime Frelaut,
  • Anne Vincent‐Salomon,
  • Charlotte Lecerf,
  • Céline Callens,
  • Samantha Antonio,
  • Coralie Franck,
  • Odette Mariani,
  • Ivan Bièche,
  • Maud Kamal,
  • Christophe Le Tourneau,
  • Vincent Servois

Journal volume & issue
Vol. 15, no. 1
pp. 104 – 115


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High‐throughput molecular profiling of solid tumours using core needle biopsies (CNB) allows the identification of actionable molecular alterations, with around 70% success rate. Although several studies have demonstrated the utility of small biopsy specimens for molecular testing, there remains debate as to the sensitivity of the less invasive fine‐needle aspiration (FNA) compared to CNB to detect molecular alterations. We aimed to prospectively evaluate the potential of FNA to detect such alterations in various tumour types as compared to CNB in cancer patients included in the SHIVA02 trial. An in‐house amplicon‐based targeted sequencing panel (Illumina TSCA 99.3 kb panel covering 87 genes) was used to identify pathogenic variants and gene copy number variations (CNV) in concomitant CNB and FNA samples obtained from 61 patients enrolled in the SHIVA02 trial (NCT03084757). The main tumour types analysed were breast (38%), colon (15%), pancreas (11%), followed by cervix and stomach (7% each). We report 123 molecular alterations (85 variants, 23 amplifications and 15 homozygous deletions) among which 98 (80%) were concordant between CNB and FNA. The remaining discordances were mainly related to deletions status, yet undetected alterations were not exclusively specific to FNA. Comparative analysis of molecular alterations in CNB and FNA showed high concordance in terms of variants as well as CNVs identified. We conclude FNA could therefore be used in routine diagnostics workflow and clinical trials for tumour molecular profiling with the advantages of being minimally invasive and preserve tissue material needed for diagnostic, prognostic or theranostic purposes.