PURPOSE KRAS, P16, TP53, and SMAD4/DPC4 mutations are common in pancreatic ductal adenocarcinoma (PDAC). The study aimed to evaluate the association between gene mutations in pretreatment Endoscopic ultrasound-guided fine needle… Click to show full abstract
PURPOSE KRAS, P16, TP53, and SMAD4/DPC4 mutations are common in pancreatic ductal adenocarcinoma (PDAC). The study aimed to evaluate the association between gene mutations in pretreatment Endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) samples and clinical outcomes of patients with PDAC. METHODS There were 43 patients with resectable (R) PDAC and 41 patients with borderline resectable (BR) PDAC. CDKN2A/p16, TP53, and SMAD4/DPC4 were evaluated through immunohistochemistry (IHC) of pretreatment EUS-FNA (n=84) and resected specimens (n=71). All patients received neoadjuvant therapy. RESULTS IHC of EUS-FNA specimens revealed p16 loss in 61 (73%), abnormal p53 in 61 (73%) and Smad4 loss in 38 (45%) patients. Abnormal p53 was associated with a lower resection rate (P = 0.017). Abnormal p53 and Smad4 loss were associated with recurrence within six months post-pancreatectomy (P = 0.03, P = 0.03, respectively). Univariate Cox regression analysis was conducted to reveal that abnormal p53 (P = 0.07), p16 loss and abnormal p53 (P = 0.04), and Smad4 and p16 loss (P = 0.03) were associated with poor prognosis. CONCLUSIONS Pretreatment abnormal labeling of p53 in EUS-FNA specimen was associated with a lower resection rate and an early recurrence in R or BR PDAC cases.
               
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