Pancreatic Cancer
Anatomy & Physiology Review
Location & Structure
Pancreas sits posterior to the stomach in the upper abdomen.
Four anatomical segments: head, neck, body, tail.
Dual (Mixed) Function
Exocrine component
Acinar cells → secrete digestive enzymes (amylase, lipase, proteases) into the pancreatic duct → duodenum.
Endocrine component
Islets of Langerhans → secrete metabolic hormones (insulin, glucagon) directly into the bloodstream.
Types of Pancreatic Cancer
Pancreatic adenocarcinoma (≈ 90–95 %)
Originates from the exocrine epithelium.
Pancreatic neuroendocrine tumors (rare)
Derive from endocrine islet cells.
Risk Factors
Modifiable
Cigarette smoking.
Excessive alcohol intake.
Chronic pancreatitis.
Diabetes mellitus.
Obesity.
Diet rich in processed meats.
Non-modifiable
Increased age.
Assigned male at birth.
Family history of pancreatic cancer.
Inherited mutations (e.g., BRCA, PALB2).
Pathophysiology & Tumor Progression
Mutations in an exocrine cell → loss of normal cell-cycle control → uncontrolled proliferation.
Tumor most commonly arises in the head; less often in body/tail.
Angiogenesis supplies the growing mass.
Local invasion: bile duct, duodenum, stomach.
Regional spread: peripancreatic lymph nodes.
Distant metastasis: especially the liver via hematogenous route.
Clinical Manifestations
General / Early
Fatigue.
Unintended weight loss.
Nausea & vomiting.
Epigastric pain radiating to the back.
Malabsorption → diarrhea (↓ pancreatic enzymes).
New-onset diabetes mellitus (↓ insulin output).
Location-specific
Head/Neck tumors
Compression of common bile duct → biliary obstruction.
Steatorrhea (foul-smelling, greasy stools) from fat malabsorption.
Obstructive jaundice: yellow skin/sclera/mucosa, pale stools, dark urine.
Courvoisier sign: enlarged, palpable, nontender gallbladder.
Body/Tail tumors
Generally silent until advanced; do not produce biliary obstruction.
Diagnostic Evaluation
History & focused physical examination.
Laboratory Findings (non-specific)
Possible ↑ serum amylase & lipase.
Tumor markers: CA 19-9, CEA.
If jaundiced: ↑ bilirubin and alkaline phosphatase (ALP).
Imaging Studies
Abdominal ultrasound, CT, MRI, endoscopic ultrasound/retrograde cholangiopancreatography.
Used for staging (T/N/M), mapping resectability, lymph node involvement, metastasis.
Definitive diagnosis = tissue biopsy of the suspicious lesion.
Treatment Overview
Prognosis: generally poor, because most tumors are advanced at diagnosis.
Localized / Resectable disease
Surgical resection is mainstay.
Whipple procedure (pancreaticoduodenectomy) for head lesions.
Partial or total pancreatectomy for body/tail or extensive disease.
Chemotherapy
Neoadjuvant: shrink tumor pre-op.
Adjuvant: eradicate residual disease post-op.
Unresectable / Metastatic disease or non-surgical candidates
Systemic chemotherapy ± radiation.
Palliative care: opioid analgesics, antiemetics, nutritional & psychosocial support.
Nursing Care
Goals: symptom control, complication monitoring, quality-of-life promotion.
Pain Management
Perform comprehensive pain assessment (onset, quality, severity, location, aggravating/relieving factors, frequency).
Position for comfort, use non-pharmacologic measures.
Administer prescribed analgesics; escalate & report if pain is uncontrolled.
Nutritional Support
Baseline assessment: weight, nausea/vomiting pattern, current intake.
Provide ordered TPN, enteral formulas, or oral diet as tolerated.
Administer pancreatic enzyme supplements with all meals/snacks.
Give antiemetics per schedule or PRN.
Surgical (Whipple / Pancreatectomy) Post-op Care
Usual resection removes: head of pancreas, gallbladder, part of duodenum & common bile duct, regional nodes; remaining structures anastomosed to jejunum.
Interventions
Semi-Fowler’s to ↓ tension on suture & anastomosis.
Maintain IV fluids ➔ correct fluid/electrolyte deficits.
NG tube on low intermittent suction; monitor patency & drainage; keep patient NPO until cleared.
Biliary drainage tube in dependent position; record color, consistency, volume.
Report any:
Bloody / clear / bile-tinged leakage (possible anastomotic breakdown).
Signs of fistula / peritonitis: board-like abdomen, severe pain, fever.
Glycemic Monitoring
Check blood glucose regularly; pancreas removal or dysfunction → labile glucose.
Administer insulin as prescribed for hyperglycemia.
Care Coordination
Collaborate with case manager for home health, palliative, hospice resources.
Facilitate family conferences, advance-care-planning discussions.
Client & Family Teaching
Pathophysiology: tumor disrupts both digestive enzyme output & hormone regulation; therapy targets symptom relief & life prolongation.
Diet strategies
5–6 small meals/day.
Eat when energy highest; consume nutrient-dense foods first.
Expected side effects: nausea, vomiting, early satiety.
Medication self-management
Timing, dosing, side-effects of analgesics, antiemetics, pancreatic enzyme capsules, insulin, chemotherapy agents.
Post-surgical home care
Site observation: redness, swelling, warmth, drainage.
Monitor biliary tube output; report blood immediately.
Support resources
Local cancer support groups, nutrition services, counseling, hospice.
Ethical / Practical Considerations
Prognostic honesty balanced with hope; emphasize quality of life.
Early palliative care referral improves symptom control & family coping.
Genetic counseling for relatives (BRCA, PALB2 mutations).
Quick Recap / High-Yield Points
Pancreatic cancer = highly aggressive, poor 5-year survival.
Major risks: smoking, alcohol, chronic pancreatitis, obesity, diabetes, processed meat diet, family/genetic syndromes.
Classic triad (head lesions): weight loss + epigastric/back pain + obstructive jaundice.
Work-up: ↑ CA 19-9, imaging (CT/MRI), confirm with biopsy.
Whipple is curative only if localized; otherwise systemic chemo + palliation.
Nursing: pain control, nutritional support, meticulous post-op monitoring, glycemic management, holistic & palliative focus.