Colorectal Cancer Flashcards

1
Q

Staging colorectal cancer?

A

TNM

Tumour
Tis
T1: invade submucosa
T2: invade muscularis
T3: through propria into subserosa or nonperitonealized pericolic or perirectal tissues
T4: directly invade other organs or structures or perforate visceral peritoneum

Nodes
N1 : metastasis in 1-3 pericolic or perirectal lymph nodes
N2: ≥ 4

Distant Metastasis
M1

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2
Q

Symptoms and Presentation colorectal cancer? (5)

A

• Suspicious symtoms/signs: weight loss, constipation, change bowel habits, Pr bleed, rectal mass, tenesmus and rectal pain
• asymptomatic discovered by routine screening
• emergency admission with complications: intestinal obstruction,obstructive symptoms (colicky pain), perforation and peritonitis, rarely acute gi bleed, abdo pain, unexplained iron deficiency anemia
• symptoms metastasis: RUQ pain, abdominal distention, early satiety, supraclavicular adenopathy, periumbilical nodules.
• unusual presentations:malignant fistula (especially caecal, sigmoid carcinoma), fever unknown origin, abscesses (intra-abdominal, retroperitoneal, abdominal wall, intrahepatic - due to localized perforated colon cancer), liver mets found incidentally

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3
Q

Treatment T1/T2 Mo rectal cancer?

A

Surgery with adjuvant chemo

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4
Q

Treatment T3/T4 Mo rectal cancer? (3)

A

• Neoadjuvant chemosensitising radiotherapy
• Surgery: lar (low anterior resection) or Apr (abdominal perineal resection)
• adjuvant chemo

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5
Q

Treatment Mo colon cancer?

A

• Surgical resection eg right hemicolectomy if resectable
• adjuvant chemo

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6
Q

Risk factors colorectal cancer? (9)

A

• Older age > 65
• smoking
• obesity
• diet: red and processed meat,
. alcohol heavy use
• IBD
• personal, family history
• colorectal polyps (premalignant)
• hereditary coloretal carcinoma syndrome eg lynch syndrome ( hereditary non-polyposis colorectal cancer hnpcc ), fap

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7
Q

Pathogenesis hereditary Colorectal cancer? (3)

A

• Chromosomal instability (CIN) pathway
• microsomal instability (msi)
• serrated pathway

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8
Q

Briefly explain CIN pathway in the pathogenesis of colorectal cancer (3)

A

Chromosomal instability. Conventional adenoma -carcinoma sequence 70%
• Inactivate mutations tumour suppressor genes eg APC (adenomatous polyposis coli) gene! → early adenoma
• activate mutations in proto-oncogenes eg KRAS! → increased clonal expansion cells → late Adenoma
• subsequent loss heterozygosity for chromosome 18q and loss tumour suppressor p53! confer these expanding cells without additional growth advantages → invasive cancer.

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9
Q

Briefly explain MSI pathway in the pathogenesis of colorectal cancer

A

Mismatch repair deficiency. Microsatellite instability pathway 3-5%
•Loss APC gene and inactivation mismatch repair (mmr)! genes eg MutL homolog 1 (MLH1) due to epigenetic silencing via promoter hyper methylation → adenoma
• mutations proliferative and differentiation target genes eg tgfbrii (transforming growth factor ß receptor 2); proteins involved in apoptosis regulation eg BAX → microsatellite unstable invasive cancer

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10
Q

Briefly explain serrated pathway in the pathogenesis of colorectal cancer (2)

A

Serrated polyp path 20- 30%
• Hypermethylation genes → Proto-oncogene BRAF mutation! → increased mapks/ ERKs signalling → cell proliferation →serrated adenoma
• methylation other genes and loss tumour suppressor genes eg tp53, p16 → cancer

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11
Q

How can colorectal cancer be screened for?

A

Faecal occult blood test from age 55. If positive → colonoscopy
(Not done in SA)

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12
Q

Most common metastatic sites of colorectal cancer? (4)

A

• Regional lymph nodes
• liver next (haematogenous dissemination via portal vein) (ruq pain, distention, early satiety)
• then lungs (distal rectum first to lungs. Inferior rectal vein drain into IVC, not portal)
• bone, peritoneum, brain

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13
Q

Most common type colorectal cancer?

A

Adenocarcinoma

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14
Q

Bloods Investigations for colorectal cancer? (5)

A

• FBC (if anemia, Pr bleed),
• UCE (bowel obstruction - electrolyte imbalance;need normal UCE for CT contrast for staging )
• LFT (need normal for chemo)
• CEA: tumour marker for monitoring during treatment and surveillance.
• HIV: cancer is an AIDS defining condition.

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15
Q

Imaging Investigations for colorectal cancer? (5)

A

• CXR: rule out cannon ball lung metastasis
• AXR: rule out bowel obstruction because will need bowel prep for colonoscopy.
• colonoscopy: id tumour site, biopsy, remove other premalignant lesions eg polyps, id impending or partial bowel obstruction that doesn’t allow scope progression, palliation impending bowel obstruction using colonic stent.
( • double contrast barium enema dcbe: was used to show apple core lesion suggestive of CRC but not done anymore, lots of complications , ct preferred )
• CT chest abdomen pelvis: staging for metastasis
• MRI: local t and N staging rectal cancers, not colon.

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16
Q

Name 4 indications adjuvant chemotherapy in colorectal cancer

A

• Metastatic
• t3 T4
•Positive lymph nodes (minimum 14 nodes in resection specimen need to be examined for tumour deposits)
• high risk features eg lymphovascular infiltration, perineural infiltration etc

17
Q

How is palliation done in colorectal cancer? (6)

A

• Analgesia as per WHO pain ladder. Most end on morphine. Prescribe laxative to relieve constipation side effect of opioid
• bowel obstruction: colonic stent or diverting loop colostomy or surgery to resect tumour or bypass it.
• obstructive jaundice (enlarged lymph nodes at porta hepatis): ercp and stent or PTC
• psychological
• rectal cancer pain: radiotherapy
• metastasis: chemotherapy to slow it down
• fecal incontinence secondary to low rectal cancers involving sphincters

18
Q

How is follow up or surveillance done for colorectal cancer? (6)

A

• Minimum 5 years every 6 months to a year.
• Clinical examination
• Blood tumour marker CEA level and trend (normal =0-5)
• CT
• colonoscopy
• pet CT if CEA increasing but ct and colonoscopy negative.

19
Q

Right vs left sided colon cancer? (6)

A

Right: occult blood in stool, abdominal pain, iron deficiency anaemia, palpable mass rif, present late bc larger size lumen so only obstruct when tumour is large
Left: rectal bleeding, tenesmus, palpable mass Lif or Pr