Diagnosis and Management of Pancreatic Ductal Adenocarcinoma
Clinical Features
- Persistent back pain, marked and rapid weight loss, abdominal mass, ascites, and supraclavicular lymphadenopathy usually indicate an incurable situation 1
- Adult-onset diabetes without predisposing features or family history may be an early indicator of pancreatic cancer 1
- Unexplained episodes of acute pancreatitis should prompt investigation for underlying pancreatic cancer 1
Diagnosis
- Ultrasound of the liver, bile duct, and pancreas should be performed without delay when clinical presentation suggests pancreatic cancer 1
- Blood counts and liver enzymes should be included in the initial workup 2
- Pancreatic protocol CT scan or MRI are the preferred imaging studies for diagnosis and staging 1
- When malignancy is suspected from clinical symptoms and/or ultrasound findings, selective use of CT, ERCP, and/or MR (including MRCP and occasionally MRA) will accurately delineate tumor size, infiltration, and metastatic disease 1
- Endosonography (EUS) may be appropriate in selected cases for better visualization of the pancreas and to obtain tissue samples 1
Pathological Diagnosis
- Pathological diagnosis should be made according to the World Health Organization classification from a biopsy or fine needle aspiration 2
- Ductal adenocarcinomas constitute 95% of pancreatic epithelial tumors 2
- Attempts should be made to obtain tissue diagnosis during investigative endoscopic procedures 1
- Failure to obtain histological confirmation does not exclude the presence of a tumor when clinical suspicion is high 1
Staging and Risk Assessment
- Staging includes complete history and physical examination, blood counts, liver enzymes, chest X-ray, abdominal imaging, and possibly endosonography 2
- TNM staging system is used, though it does not well reflect tumor resectability 2
- Evaluation of resectability often requires surgery, preferably staging laparoscopy to exclude clinically occult intra-abdominal and lymph node metastases 2
- Resectable tumors must show no evidence of extra-pancreatic disease, direct tumor extension to the celiac axis and superior mesenteric artery, or non-obstructive invasion of the superior mesenteric-portal vein confluence 2
- Less than 20% of patients have resectable disease at diagnosis 2, 3
Management
- Complete surgical resection is the only potentially curative treatment available 2
- Five-year overall survival after resection is only 10-20% 2
- Long-term survival in lymph node positive (N+) tumors is rare 2
- Gemcitabine has been associated with a small survival benefit compared with bolus 5-fluorouracil 2
- Optimal symptomatic treatment has a prime role in management 2
- Stenting or bypass surgery may be required for obstructive jaundice or gastric outlet obstruction 2
Follow-up
- Due to the limited effectiveness of treatments, follow-up after complete resection should be restricted to history and physical examination 2
- Response evaluation should be symptom-driven rather than based on radiographic tests alone 2
Special Considerations
- Patients at increased inherited risk of pancreatic cancer should be referred to specialist centers offering genetic counseling and appropriate testing 1
- Secondary screening for pancreatic cancer in high-risk cases should be carried out as part of an investigational program coordinated through specialist centers 1
- Examination and biopsy of the periampullary region is important in patients with longstanding familial adenomatous polyposis 1
- Continued health education to reduce tobacco consumption should lower the risk of developing pancreatic carcinoma 1