Pancreatic Cancer Nutrition (Week 8 Lecture 2) Flashcards

1
Q

What is PDAC, PEI and PERT?

A
  • pancreatic adenocarcinoma
  • pancreatic exocrine insufficiency
  • Pancreatic Enzyme Replacement Therapy
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2
Q

Prevalence of malnutrition in PDAC

A

> 80% of PDAC pts have significant weight loss with severe malnutrition and cancer cachexia at diagnosis.

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3
Q

What factors play into malnutrition?

A

psychological factors, metabolic factors, gastrointestinal factors
* sarcopenia
* cachexia
* ↓ immune competence and QOL
* ↑ infections, stress, treatment toxicity and mortality

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4
Q

Describe sarcopenia and potential outcomes

A
  • can occur concurrently with obesity
  • ↑ incidence of chemo related toxicity
  • shorter time to tumour progression
  • physical disability
  • poor surgical outcomes
  • ↓ survival
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5
Q

2 main pancreatic functions

A
  • Exocrine: produce and secrete digestive enzymes/juices (protease, amylase, lipase, water and bicarbonate)
  • Endocrine: produce and secrete hormones for digestion (insulin, glucagon, gastrin and amylin)
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6
Q

Describe pancreatic cancer

A

95% of pancreatic cancers are exocrine tumours, with 90% being adenocarcinoma (PDAC), originating from ductal tissue (originates in head from ductal tissue)
* Important to consider location of tumour, ductal dilation, state of remaining pancreas and overall tumour burden (head will have biggest impact, rest of pancreas is atrophic)

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7
Q

What are the main types of pancreatic cancer?

A

2 main types of PDAC:
1. Unresectable/metastatic - too much vascularizationfrom the malignancy and unable to remove
* Palliative bypass (may be deemed this for years)
2. Curative/Surgical:
* Whipple (classic or pylorus preserving-head of pancreas, gallbladder, duodenum is removed and liver, and stomach attached to the jejunum. So can still have some pancreas left)
* Total Pancreatectomy (acute type of diabetes)
* Distal pancreatectomy (just tail removed and then most of exocrine remains)

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8
Q

Describe PEI

A

A condition caused by reduced or inappropriate secretion or function of pancreatic juices and its digestive enzymes causing maldigestion
* lipase in particular, protease, amylase and likely bicarbonate
* Can be caused by decreased production of pancreatic enzymes, blockage due to mass, or surgery/removal of enzyme producing cells

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9
Q

Prevalence of PEI

A
  • 90 - 100% locally advanced or metastatic pancreatic cancer (exocrine insufficiency). Increased risk factors, head localized, larger size, ductal obstruction, coexistent chronic pancreatitis
  • Post-operative PDAC patients: 80-90% of Whipple pts, 20-50% distal pancreatectomy, 100% total pancreatectomy.
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10
Q

What are some outcomes of PEI?

A

Impact of PEI in pts with PDAC is associated with malnutrition, sarcopenia, fat degradation, longer hospital stays, increased risk of complication, reduced response to treatment, decrease QOL, increase risk of morbidity and mortality in both unresectable and resectable pts.
* Associated with decreased QOL, nutrition, post-op survival and cancer related outcomes.
* Post PEI may impede ECOG and ability to initiate adjuvant chemotherapy

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11
Q

Abdominal symptoms of PEI

A
  • Diarrhea
  • Steatorrhea (oily, pale, floating)
  • Fecal urgency
  • Bloating, gas, foul smelling
  • Reflux
  • Cramping abdominal pain or gurgling post intake (57%)
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12
Q

Endocrine symptoms of PEI

A
  • Hypoglycemia
  • Decreased insulin requirements for pre-cancer diabetics
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13
Q

nutrition symptoms of PEI

A
  • Unexplained weight loss (even if still eating)
  • Sarcopenia
  • Weakness, fatigue
  • Food avoidance (due to fear of digestive symptoms)
  • Vitamin deficiency - fat soluble vitamins
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14
Q

What is the treatment for PEI?

A

Pancreatic enzyme replacement therapy (PERT) are prescribed by the doctor, with/without help of specialized dietitian, exact dosing is still not well established. Should be defined based on improvement of identified PEI symptoms.
* Pancreatic enzymes used commonly: Creon (10, 25, 35), Cotazym ECS (8, 20)
* enterically-coated needed for oral use (other than post gastrectomy); need coating to prevent degradation
* Each pancreatic enzyme capsule contains combination of lipase, protease, amylase

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15
Q

How is PERT dosing determined?

A

PERTdosing recommendations primarily based on CF population but assume pancreatic patients will need more; for CF based on kg BW x units of lipase per meal or with a total daily limit.
* 500-2500 units of lipase per kg/meal or 10,000 units per kg/day
* Use half calculated meal dose for snacks
* Risk associated with exceeding, constipation
* Starting dose for pancreatic patients is 40,000 – 50,000 USP/meal, 25,000 USP/snack
* Start conservatively and increase slowly

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16
Q

Outcome of PERT

A
  • Side effects when starting enzymes: bloating, cramping, fullness, nausea, hyperglycemia
  • Evaluating response to enzymes should be routine → signs of PEI symptoms
  • PERT will cause large volume soft stools. Pt must be aware of this
  • Dietary fat restriction is not indicated or recommended
17
Q

How is PERT taken?

A

PERT is needed with all solids or liquids that contain complex carbohydrates, fat or protein. They should be taken right before onset of intake.
* Do not need to be taken with sugar only (refined CHO) foods: popsicle, hard candy, fruit juice, pop
* Slightly higher doses may be needed with foods that are high in fat/protein or larger meals/snacks, start by adding 1-2 for meal, 1 for snack.
* Patients need education before initiating this treatment!

18
Q

Assessing and adjusting PERT

A
  • Follow up: Follow up on enzyme therapy initiation within ~ 2 weeks of start (my current practice). Assess for symptom improvement, review titration and dose up if indicated.
  • Increase: Enzyme doses may need to increase with disease progression or organ atrophy. Important patient understands dose may need to change.
  • Switch: If started on low concentration PERT, once dose range established can switch to higher concentration to reduce number of capsules needed. I leave this to patient choice.
19
Q

How to ensure patients are taking PERT properly

A
  • Timing: right before starting oral intake, can try up to 30min prior. Effective for up to 1hr. If out for social style meals that have multiple courses or take >1hr, multiple smaller doses will be needed.
  • Frequency (all meals/snacks), often patients miss doses with snack, liquids
20
Q

How to adjust PERT if it was effective then symptoms return

A

If patient had been finding effective, then PEI symptoms return or new upper GI symptoms of GERD or burping, consider adding PPI. This is related likely to bicarbonate secretion dysfunction.
* If ongoing weight loss despite PERT and PPI, ensure blood supar is assessed and monitored