Big 4 - Colorectal Cancer Flashcards

1
Q

What is the incidence of bowel cancer?

What is the survival after 1 year and 5 years like?

A

1 in 20 people will get bowel cancer during their life time

  • the 1 year survival is 75-80% which is considered to be quite good
  • the 5 year survival is 60%
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2
Q

Which groups are more likely to get colorectal cancer?

A
  • the incidence increases with age
  • it is more common in males
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3
Q

How is the mortality changing over time?

A
  • mortality rates are decreasing over time due to more effective screening programmes and better treatments
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4
Q

How is colorectal cancer staged?

A

TNM system

  • T stage is how far the tumour has eroded through the bowel wall
  • N stage is based on the number of lymph nodes involved
  • M stage is based on the extent of metastases and the organs involved
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5
Q

How can the T stage further be subdivided from T1 to T4?

A

Tis:

  • this is carcinoma in situ - the tumour is only within the mucosa

T1:

  • the tumour is only in the inner layer of the bowel

T2:

  • the tumour has grown into the muscular layer of the bowel wall

T3:

  • the tumour has grown into the outer lining of the bowel wall but has not grown through it

T4a:

  • the tumour has grown through the outer lining of the bowel wall and into the peritoneum

T4b:

  • the tumour has grown through the outer lining of the bowel wall and into nearby organs
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6
Q

How can the N stage be further subdivided into N0-N2?

A

N0:

  • there are no lymph nodes containing cancer cells

N1a:

  • there are cancer cells in 1 nearby lymph node

N1b:

  • there are cancer cells in 2 or 3 nearby lymph nodes

N1c:

  • the nearby lymph nodes do not contain cancer, but there are cancer cells in tissue near the tumour

N2a:

  • there are cancer cells in 4 to 6 nearby lymph nodes

N2b:

  • there are cancer cells in 7 or more nearby lymph nodes
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7
Q

How can the M stage be further subdivided?

A

M0:

  • the cancer has not spread to other organs

M1a:

  • the cancer has spread to 1 distant site / organ but not to the peritoneum

M1b:

  • the cancer has spread to 2** distant sites / organs but **not to the peritoneum

M1c:

  • the cancer may have spread to distant organs and has spread to the peritoneum
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8
Q

How does the stage that the cancer is detected influence survival rate?

A
  • survival rates are influenced by the stage at the time the cancer is picked up
  • there is a much better prognosis if a cancer is picked up early
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9
Q

How does bowel cancer develop?

A
  • there is a progression from benign polyps to invasive cancer
  • the tumours develop through a multistep process involving histological, morphological and genetic changes that accumulate over time
  • polyps are well-demarcated and round, whereas tumours are much more invasive
  • polyps are removed to prevent later development of cancer
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10
Q

What types of polyps are at a higher risk for developing into colorectal cancer?

What other factors increase this risk?

A
  • adenomatous polyps can change into cancer so are called a pre-cancerous condition
  • hyperplastic and inflammatory polyps are not pre-cancerous
  • polyps >1cm are more likely to become cancer
  • if more than 3 polyps are found, this increases the risk
  • if dysplasia is seen in the polyp after it has been removed
    • the cells look abnormal, but they have not yet become cancer
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11
Q

How can colorectal cancer spread once it forms within a polyp?

A

the cancer will grow from the polyp into the wall of the colon / rectum over time

  • the cancer starts in the mucosa (innermost layer) of the bowel and grows outward through some or all of the other layers
  • when cancer cells are in the wall, they can grow into blood or lymph vessels, allowing them to travel to lymph nodes or distant parts of the body
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12
Q

What is the most common type of colorectal cancer?

A

most colorectal cancers are adenocarcinomas

  • these start in the cells that make mucus to lubricate the inside of the colon and rectum
  • adenocarcinomas always form in glandular tissue that lines certain internal organs and releases substances into the body
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13
Q

What are the risk factors associated with colorectal cancer?

A
  • obesity
  • lack of physical activity
  • diet high in red / processed meats
  • smoking
  • excessive alcohol consumption
  • advancing age
  • personal history of inflammatory bowel disease
  • personal history of adenomatous polyps or cancer
  • family history of adenomatous polyps or cancer
  • inherited syndromes - Lynch syndrome and FAP
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14
Q

What is Lynch syndrome caused by?

(hereditary non-polyposis colon cancer)

What other conditions can this cause?

A
  • caused by a defect in the MLH1, MSH2 or MSH6 gene that usually help to repair damaged DNA
  • cancers linked to this syndrome develop when a person is relatively young
  • there may be polyps present, but usually only a small amount
  • also strongly linked to endometrial cancer, as well as ovarian, stomach, pancreatic, kidney, prostate, breast…and more
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15
Q

What causes familial adenomatous polyposis (FAP)?

When do these people tend to develop colon cancer and why?

A
  • caused by changes in the APC gene that a person inherits from their paretns
  • 100s-1000s of polyps develop in the colon and rectum, starting as early as 10-12 years
  • cancer usually develops in 1 or more of the polyps by the age of 20
  • by age 40, nearly all people will have colon cancer if their colon hasn’t been removed
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16
Q

Which parts of the colon are most commonly affected by colon cancer?

A
  • tumours are much more common in the left colon** and **rectum
  • around 1/3 occur in the rectum, 1/3 on the left side and 1/3 in the remainder of the colon
17
Q

What are the 6 main red flag symptoms associated with colorectal cancer?

A
  • rectal bleeding
  • change in bowel habit / unable to fully empty bowels
  • abdominal pain
  • mucous PR
  • anorexia
  • weight loss
18
Q

What is significant to remember about someone presenting with rectal bleeding?

A
  • it is a common symptom of cancer, but can also be caused by other things:
    • anal fissure
    • haemorrhoids
    • trauma
    • anticoagulants
    • gastroenteritis
  • 40-50% of the population will have PR bleeding at some point
19
Q

What signs of colorectal cancer might be present on examination?

A
  • systemic signs of cancer, such as anaemia and weight loss
  • abdominal mass / fullness
  • mass, ulcer or stricture on rectal examination
20
Q

What would be the next stage of investigation for someone presenting with red flag symptoms?

A

referral via the urgent 2 week-wait cancer referral pathway

  • if patient is fit and well, they will have a colonoscopy / flexible sigmoidoscopy
  • if they are less well, they will have a colorectal surgeon / gastro review within 14 days

if cancer is diagnosed, treatment must start within 62 days

21
Q

How might someone with colon cancer present as an emergency?

What is the concern associated with this?

A
  • 1 in 5 have red flag symptoms, and they tend to present with:
    • bleeding
    • obstruction
    • perforation
    • abdominal pain
  • these cancers are typically much more advanced, and so carry a worse prognosis
22
Q

What is involved in the screening for colorectal cancer?

What % of cancers does this detect?

A
  • faecal immunochemical testing (FIT) requires a single sample
  • individuals aged 60-74 are invited to do this test every 2 years
  • if the sample is positive, it is treated as urgent suspected cancer (2WW)
  • detects 10% cases of cancer, 44% are at an early stage
23
Q

What other screening programme has been introduced recently for younger individuals?

A

bowel screening scope (sigmoidoscopy)

  • this is a one-off test to detect left-sided polyps offered at 55
  • if it is normal, continue into bowel screening at 60
24
Q

If abnormal tissue is seen during colonoscopy, what is done?

A
  • a biopsy is taken at the point of colonoscopy to confirm the diagnosis
  • this is the only test that can definitively diagnose the cancer
25
Q

After diagnosis, why might a CT scan be performed?

A
  • CT of the thorax, abdomen and pelvis is performed to stage the cancer and look for signs of metastasis
  • this can measure the size of the tumour
  • it is often performed prior to surgery
26
Q

What is the definitive imaging modality used for colorectal cancer and why?

A

MRI is used for the pelvic staging of colorectal cancer

  • soft tissue is easier to visualise on MRI compared to CT
  • can assess nodal involvement, vascular invasion and how far the tumour extends outside of the bowel wall
27
Q

What is the CRM?

A

circumferential resection margin

  • this is the plane that the surgeons will resect around to ensure that the tumour is completely removed
  • tumour involvement of the CRM affects treatment of these patients
28
Q

Why are colon and rectal cancers treated differently?

A
  • local recurrence of colon cancers is uncommon
  • local recurrence of rectal cancers is more common
  • radiotherapy is used in rectal cancers to prevent local recurrence
29
Q

What is the typical treatment for colon cancer?

A
  • typically, all patients go straight to surgery
  • this may be a hemicolectomy or anterior resection
  • neoadjuvant chemotherapy prior to surgery is considered in those with advanced disease (T3/T4 or node positive)
30
Q

How does the treatment for rectal cancer differ from colon cancer?

A
  • neoadjuvant treatment prior to surgery is usually given to prevent the risk of recurrence

Low risk:

  • typically go straight to surgery - anterior resection, APER or Hartmanns

Moderate risk:

  • neoadjuvant treatment with radiotherapy to prevent recurrence prior to surgery
  • surgery within 1 week of the course of radiotherapy

High risk:

  • neoadjuvant therapy with radiotherapy + chemotherapy to shrink the tumour prior to surgery
  • in these patients, there is involvement of the CRM
31
Q

How is it decided whether a patient will have adjuvant chemotherapy following surgery for rectal cancer?

A
  • low risk patients possess no benefit from adjuvant chemotherapy
  • moderate risk patients have a small benefit from chemotherapy, and should be discussed within the MDT
  • high risk patients have an absolute benefit from chemotherapy as they are at the greatest risk of recurrence
32
Q

What is the typical chemotherapy regime given to high risk rectal cancer patients?

A

3 months of adjuvant chemotherapy following surgery

  • this can be single agent or dual agent
    • this depends on RFs, age of patient and cormorbidities
  • single agent involves 5FU and folic acid or oral capecitabine (same as 5FU)
  • combination therapy involves capecitabine or folinic acid / 5FU plus oxaliplatin
33
Q

What is DPD testing and why is it performed prior to chemotherapy?

A
  • all patients receiving 5FU chemotherapy are offered DPD testing
  • it tests for deficiency of the DPD enzyme
  • deficiency results in the inability to metabolise 5FU, resulting in severe toxicity from chemotherapy and extreme side effects
34
Q

Following treatment, what follow-up investigations are performed in someone with colorectal cancer?

A
  • CEA is performed every 6 months
    • this is a tumour marker to look for recurrence
  • intermittent CT staging investigations at 18 months, 3 years, 5 years
  • complete colonoscopy within 12 months, with another one 3 years later
35
Q

How does a carcinoembryomic antigen (CEA) test work?

A
  • carcinoembryonic antigens are produced by some types of cancer, including bowel cancer
  • the CEA test is carried out after surgery
  • it measures the level of CEA in the blood to check how well the treatment is working and look for signs of recurrence
36
Q

What is the treatment for someone who has a single metastasis, versus multiple metastases?

A

Single site:

  • tends to involve surgery to resect the metastatic tumour
  • 5 year survival of up to 40%

Multiple sites:

  • this is treated palliatively
  • can either do nothing or consider systemic chemotherapy
37
Q

What is involved in systemic chemotherapy as a palliative treatment?

What are the risks and benefits to this?

A
  • chemotherapy is offered to patients who are symptomatic
  • it can increase life expectancy from 6-9 months with no treatment to 18-24 months +
  • however, it is associated with multiple procedures:
    • multiple hospital visits
    • toxicity
    • inverventions - e.g. insertion of in-dwelling catheter
    • multiple scans
    • blood tests
38
Q
A