Diagnostic value of CA19.9, circulating tumour DNA and circulating tumour cells in patients with solid pancreatic tumours

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Sefrioui, David | Blanchard, France | Toure, Emmanuel | Basile, Paul | Beaussire, Ludivine | Dolfus, Claire | Perdrix, Anne | Paresy, Marianne | Antonietti, Michel | Iwanicki-Caron, Isabelle | Alhameedi, Raied | Lecleire, Stéphane | Gangloff, Alice | Schwarz, Lilian | Clatot, Florian | Tuech, Jean-Jacques | Frébourg, Thierry | Jardin, Fabrice | Sabourin, Jean-Christophe | Sarafan-Vasseur, Nasrin | Michel, Pierre | Di Fiore, Frédéric

Edité par CCSD ; Cancer Research UK -

International audience. Background: The direct comparison of CA19.9, circulating tumour cells (CTCs) and circulating tumour DNA (ctDNA) using endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) has never been performed for the diagnosis of solid pancreatic tumours (SPTs).Methods: We included 68 patients with a SPT referred for EUS-FNA. CTCs were analysed using size-based platform and ctDNA using digital PCR. The sensitivity, specificity, negative and positive predictive values were evaluated for each marker and their combination.Results: SPTs corresponded to 58 malignant tumours (52 pancreatic adenocarcinoma (PA) and 6 others) and 10 benign lesions. The sensitivity and specificity for PA diagnosis were 73% and 88% for EUS-FNA, 67% and 80% for CTC, 65% and 75% for ctDNA and 79% and 93% for CA19.9, respectively. The positivity of at least 2 markers was associated with a sensitivity and specificity of 78% and 91%, respectively. CtDNA was the only marker associated with overall survival (median 5.2 months for ctDNA þ vs 11.0 months for ctDNA , P 1⁄4 0.01).Conclusions: CA19.9 alone and in combination with ctDNA and/or CTC analysis may represent an efficient method for diagnosing PA in patients with SPTs. Further studies including a larger cohort of patients with both malignant and benign lesions will be necessary to confirm these promising results.

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