Endoscopic ultrasound (EUS)-guided fine-needle aspiration (FNA) of the pancreas allows the diagnosis of pancreatic cancer
to be established without exploratory surgery. We reviewed our recent experience with EUS-FNA in patients with presumed pancreatic
cancer and report the diagnostic accuracy and complications of this procedure. Data were reviewed from all patients who presented
with CT evidence of a pancreatic mass or a malignant biliary stricture and underwent EUS-FNA at our institution between November
1, 1999, and October 1, 2001. Based on the findings of contrast-enhanced, multislice CT scanning, patients were categorized
as having resectable, locally advanced, or metastatic disease. EUS-FNA was performed in 233 patients. A final diagnosis of
cancer was established in 216 patients (93%), 15 patients (6%) were found to have benign disease, and the final diagnosis
remains unknown in two patients (1%). The sensitivity, specificity, and accuracy of EUS-FNA for diagnosis of a pancreatic
malignancy were 91%, 100%, and 92%, respectively. For the 216 patients subsequently proven to have cancer, the results of
EUS-FNA were diagnostic in 197 (91%); 96 (90%) of 107 patients with resectable disease, 62 (97%) of 64 with locally advanced
disease, and 39 (87%) of 45 with metastatic disease. Four patients (2%) developed a clinically apparent complication that
required hospital admission, including two patients who required surgery for duodenal perforation. There were no EUS-related
deaths. We conclude that EUS-FNA can safely and accurately establish a cytologic diagnosis in patients with both early-stage
and advanced pancreatic cancer. This enables consideration of all treatment options including protocol-based therapy
Key words Endoscopic ultrasonography - fine-needle aspiration - pancreatic cancer
Presented at the Forty-Third Annual Meeting of The Society for Surgery of the Alimentary Tract, San Francisco, California,
May 19–22, 2002 (oral presentation).
Supported by The Lockton Fund for Pancreatic Cancer Research at The University of Texas M. D. Anderson Cancer Center.