British Journal of Cancer · 2017 · 121 citations · 39 references
MedicineOncologyPathologyGastrointestinal OncologyMolecular DiagnosticsNeoplasiaCancer DiagnosisCancer Molecular DiagnosticsCirculating Tumor CellsCirculating Tumor Dna AnalysisPancreatic CancerTumor MarkersCirculating Tumor Cell CharacterizationCirculating Tumor Cell MonitoringCirculating Tumor Dna DetectionCirculating Tumor Dna TestingCirculating Tumor MarkersDigital PcrEndoscopic Ultrasound-guided Fine-needle AspirationPositive Predictive Value
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+ vs 11.0 months for ctDNA-, P=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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Detection of Circulating Tumor DNA in Early- and Late-Stage Human Malignancies
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The clinical utility of the CA 19-9 tumor-associated antigen.
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