Bowel Cancer Flashcards

1
Q

Ten year survival rate for bowel cancer

A

53%

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2
Q

Polyp

A

is a projecting growth of tissue from a surface in the body usually a mucous membrane and can develop in the colon, rectum, ear canal, cervix, stomach, nose, uteruses, throat and bladder

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3
Q

Adenomatous polyps in the large bowel are cancerous.

True or False?

A

False
precancerous but only 5% progress into cancer can be 10 years

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4
Q

Colorectal cancer begins with the formation of a

A

small fixed adenoma

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5
Q

Pathogenesis of Bowel Cancer:

A
  • small adenomas could progress into more advances,
    more giant fixed adenomas
  • all adenomatous polyps have dysplasia, size is not
    relevant, though larger polyps may be more likely to
    have high grade dysplasia
  • some cancers will be seen in very small polyps and
    many large polyps do not have cancer or even high
    grade dysplasia
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6
Q

Adenoma-carcinoma sequence

A
  • low grade dysplasia to high grade dysplasia, CRC

***APC inactivation

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7
Q

adenoma carcinoma sequence

A
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8
Q

Screening and prevention of bowel cancer (wilson’s criteria):

A
  • identification of a pre-malignant phase (polyp)
  • there is a good and acceptable test (colonoscopy)
  • there is an agreed and acceptable treatment
    (polypectomy)
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9
Q

serrated pathway in colorectal cancer

A
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10
Q

Genetics of colo-rectal cancer:

A
  • 75% are sporadic
  • 20% of CRC patients report a family history of the
    disease
  • 3-5% are hereditary due to the highly penetrant
    germline mutations
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11
Q

Two forms of hereditary colorectal cancer:

A
  • polyposis
  • lynch syndrome
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12
Q

Polyposis:

A
  • familial adenomatous polyposis (FAP)are caused by
    pathogenic varients in APC gene which is
    chromosome 5q21
  • MUTHY-associated polyposis: caused by pathogenic
    variants in the MUYTH gene
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13
Q

What does the APC gene do?

A
  • APC gene provides instructions for making the APC
    protein, which is critical in several cellular processes
  • the apc protein acts as a tumour suppressor and
    keeps cells from growing and dividing too fast or
    uncontrolled
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14
Q

Lynch syndrome (hereditary nonpolyposis colorectal cancer):

A
  • caused by germline pathogenic varients in DNA
    mismatch repair genes (MMR genes and EPCAM)
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15
Q

Two Hit Hypothesis

A
  • two genetic abnormalities are required (both copies
    of the affected gene) to develop certain cancers
  • those with a hereditary susceptibility to cancer inherit
    a damage chromosme , hence their first hit occurs at
    conception, whereas others may receive their first hit
    at a later stage
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16
Q

Two hit theory of cancer causation

A
17
Q

Familial Adenomatous Polyposis (FAP):

A
  • autosomal dominant
  • 25% are new mutations; no family history
  • > 100 polyps by late teens
  • almost 100% risk of bowel cancer by 30
  • surgery is reccomended by the 20s
  • screening for cancers/polyps in stomach, small bowel
    and thyroid
18
Q

Lynch syndrome (hereditary nonpolyposis colorectal cancer):
-what % of cases are new mutations?
- does or doesnt follow two hit hypothesis?
- increases risk of what type of cancers?

A
  • 20% are new mutations
  • follows two hit hypothesis
  • increases risk of endometrial and renal cell cancer,
    sometimes breast, upper GI and prostate
19
Q

Bowel Cancer Staging:

A
  • TNM
  • tumour: has the tumour grown into the wall of colon
    or rectum? How many layers (serosa etc)?
  • nodes: has the tumour spread to the lymph nodes?
    where and how many?
  • metastasis: has the cancer spread to other parts of
    the body? Where and how much?
20
Q

Distant metastasis sites of colorectal cancer?

A
  • brain
  • lungs
  • liver (most)
  • spleen
  • mesentery (omentum)
  • bone
21
Q

Bowel Cancer: Risk factors:

A
  • higher incidence in western world, and white
  • roughly equal in both men and women
  • 2/3 occur in those over 60
  • genetics: polyposis like FAP
  • longstanding inflammatory bowel disease like UC
22
Q

What % of bowel cancer is preventable in the UK?

A

54%
(meat, alcohol, smoking)

23
Q

High dietary fibre reduces the risk of bowel cancer:

A
  • increases the formation of short chain fatty acids
  • reduce stool transit time
  • reduces secondary bile acid formation
24
Q

High dietary fibre reduces the risk of bowel cancer: increases the formation of short chain fatty acids:

A
  • promotes healthy gut bacteria, which can induce cell
    differentiation, arrest cell growth and cause apoptosis
  • reduce proliferation of neoplastic cells
25
Q

High dietary fibre reduces the risk of bowel cancer: reduce stool transit time:

A
  • carcinogens are common in food, faster transit means
    less time for these to act on the bowel mucosa
26
Q

High dietary fibre reduces the risk of bowel cancer: reduces secondary bile acid formation:

A
  • potentially carcinogenic
27
Q

Clinical features of bowel cancer:

A
  • changes in bowel movements
  • gas/bloating
  • abdo discomfort
  • nausea/vomiting
  • fatigue
  • weight loss
  • loss of appetite
  • anaemia
  • cramping
28
Q

Clinical features of Rectal cancer:

A
  • rectal bleeding
  • change in bowel habits
  • rectal pressure or fullness
  • thin or ribbon like stools
  • anaemia
  • cramping
  • weight loss
  • loss of appetite
  • fatigue
29
Q

Clinical presentation of bowel cancer:

A
  • > 60:
    • iron deficiency anaemia
    • change in bowel habit
  • > 50:
    • unexplained rectal bleeding
  • <50:
    • unexplained rectal bleeding
    • abdominal pain
    • change in bowel habits
    • weight loss
    • iron deficiency anaemia
  • > 40:
    • weight loss and abdo pain
  • any age with abdo or rectal mass
30
Q

Bowel Cancer Screening:

A
  • 60-74
  • every two years
  • qFIT
  • detects human goblin (amount of blood in stool)
  • > 75 can request one every two years
31
Q

Limitations of qFIT:

A
  • 50% patients with documented colorectal cancers
    have a negative faecal occult blood test, consistent
    with the intermittent bleeding pattern of these
    tumours
32
Q

If qFIT is positive then definitely cancer/

True or False?

A

False
follow up tests required to determine the reason for the presence of blood in the stool

33
Q

Further investigations for bowel cancer:

A
  • qFIT
  • physical exam
  • colonoscopy “goldstandard”
  • biopsy
  • biomarker testing to identify specific genes, unique
    factors of tumour
  • blood tests: anaemia (due to bleeding)
  • ultrasound, CXR, CT, MRI