Colorectal Cancer Flashcards

0
Q

CRC Pathophysiology

A
  • normal colon
  • > hyperproliferative epithelium
  • > adenoma
  • > carcinoma
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1
Q

Colorectal Cancer Aetiology

A
  • environmental influences: high dietary fat, low dietary fibre
    • genetic influences:
      • all colorectal cancers considered to have genetic component, to varying degrees
      • genetic changes implicated:
        • activation of proto-oncogenes (K-ras)
        • loss of tumour-suppressor gene activity (APC, DCC)
        • abnormalities in DNA repair genes (hMSH2, hMLHl), especially HNPCC syndromes
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2
Q

CRC Risk Factors

A
  • 75% have no known risk factors
    • age
    • adenomatous polyps
    • family history
    • IBD
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3
Q

CRC Age Risk Factor

A
  • 90% of cancers are in people >50 yrs old

* at age 50, the risk of developing colorectal cancer by age 80 is 5%

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4
Q

CRC Family History Risk Factor

A
  • sporadic cancer
    * risk increases 1.8x for those with one affected relative, 2-6x with two affected relatives
    * risk is greater if relative has cancer diagnosed < 45 yrs old
    • FAP (familial adenomatous polyposis) and Gardner’s syndrome
    • HNPCC (hereditary nonpolyposis colorectal cancer) or Lynch syndrome
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5
Q

CRC IBD Risk Factor

A
  • UC - after 10 yrs, cancer risk increased approximately by 1% for each additional year
    • Crohn’s disease - unclear, likely similar to UC if more than 1/3 of colon inflammed
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6
Q

CRC Prevention

A
  • Lifestyle modifications
    • ASA
    • Screening - Average risk and above-average risk
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7
Q

CRC Lifestyle Modifications

A
  • increase fibre in diet
    • decrease animal fat and red meat
    • decrease smoking and EtOH
    • increase exercise
    • decrease BMI
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8
Q

CRC Screening for at average risk individuals

A
  • > 50 years with no family history
    • FOBT q2yrs
    • Colonoscopy q10yrs
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9
Q

CRC Screening for above average risk individuals

A
  • HNPCC
    * Genetic testing + colonoscopy q2yrs beginning at age 20
    • FAP
      • Genetic testing + sigmoidoscopy annually beginning at age I0-12
    • Fam Hx of cancer
      • (1+ 1st degree relatives with CRC i.e. parent, sibling or child) or polyps but does not fit criteria for HNPCC/FAP
      • colonoscopy q5yrs beginning at age 40 or 10yrs earlier than the youngest diagnosed polyp/cancer case in the family.
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10
Q

CRC Staging and 5 year Prognosis

A
  • Dukes Staging with 5 year survival
    * Dukes A (limited to submucosa): 80-95%
    * Dukes B (penetrating serosa): 55-67%
    * Dukes C (into lymph nodes): 30-45%
    * Dukes D (metastases): 1%
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11
Q

CRC Treatment

A
  • Surgery
    * surgery (indicated in potentially curable or symptomatic cases- not usually in stage IV)
    • Radiotherapy and Chemotherapy
      • alone not curative
    • Surveillance
      • When polyps are found
      • Colonoscopy 3 yrs after initial finding and then q5yrs
    • Past CRC
      • Colonoscopy q3-5yrs
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