GI Cancers Flashcards

1
Q

How are GI cancers generally staged?

A

Depth of penetration and then degree of spread

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2
Q

What is the globally recognized staging of malignant tumors?

A

T - size of original tumor
N - lymph node invovlement
M - metastasis

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3
Q

Most GI cancers arise from what layer?

A

Epithelial

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4
Q

Most GI cancers are what type?

A

Adenocarcinoma

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5
Q

Upper and mid esophageal cancers are mostly what type?

A

Squamous cell

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6
Q

Risks for esophageal cancer?

A

Tobacco 10x

ETOH 100x

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7
Q

MC type of esophageal cancer in the US?

A

Adenocarcinoma of distal esophagus or GE junction

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8
Q

What is adenocarcinoma of the distal esophagus/GE junction a/w?

A
  • Reflux and dysplastic changes of mucosa

- Barrett Esophagus

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9
Q

Evaluation and staging of esophageal cancer

A
  • Barium swallow showing “esophageal shelf”
  • EGD w/biopsy
  • If cancer found, endoscopic ultrasound to stage depth of invasion
  • CT scan to look for mets
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10
Q

Treatment of T0/high grade dysplasia/T1 adenocarcinoma of esophagus?

A
  • Endoscopic ablation

- Esophageal resection

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11
Q

How do most cancers of the esophagus present?

A

At stages higher than T0/high grade dysplasia/T1 adenocarcinoma

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12
Q

Treatment of higher stages esophageal cancer?

A
  • RT or chemo-RT

- Stage IV: Palliative

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13
Q

Prognosis of T0 and T1 esophageal cancer

A

5 year survival is 98%

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14
Q

Prognosis of stage II and III esophageal cancer

A

Median survival is approx 4 years with tri-modality treatment of chemo-RT and then esophagectomy

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15
Q

Stage IV esophageal cancer prognosis

A

Median survival is approx 9 months

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16
Q

Where is gastric cancer a common problem?

A

Japan and some other areas of Asia

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17
Q

Risks for gastric cancer

A
  • Diets LOW in Vit A and C
  • Consumpton of smoked/cured foods
  • Tobacco
  • Untreated H. pylori
  • Genetic (Type A blood, pernicious anemia, HNPCC)
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18
Q

MC type of gastric cancer?

A

Adenocarcinoma (95% cases)

  • Diffuse infiltration (linitus plastica)
  • Polypoid or ulcerative masses (intestinal)
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19
Q

Clinical presentation of gastric cancer

A
  • Melena
  • Ascites of unclear etiology
  • Virchow’s node
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20
Q

What is needed for diagnosis of gastric cancer?

A

Endoscopic biopsy

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21
Q

What is Virchow’s node and what does it indicate?

A
  • L supraclavicular adenopathy

- Gastric, pancreatic cancer

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22
Q

Prevention of gastric cancer?

A
  • Screening EGD in endemic areas (e.g. Japan)

- Treat H. pylori infections

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23
Q

Treatment of Stage I-III gastric adenocarcinoma

A

Surgical resection

  • D1 in the US (and adjuvant chemo-RT)
  • D2 in Japan
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24
Q

When does gastric cancer typically present?

A

6th decade

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25
Describe gastric lymphoma
- Relatively rare - Submucosal or ulcerated mass - Histologically most are MALT - H. pylori etiology MC
26
Treatment of gastric lymphoma
- Eradicate H. pylori - 75% will achieve CR with abx - High grade lymphomas are treated with multi-agent chemo (40-50% 5 yr survival)
27
MC type of small bowel cancer
Adenocarcinoma
28
What types of small bowel cancer arise from polyps?
Autosomal dominant: - Gardener's syndrome - Peutz-Jeghers syndrome
29
What are carcinoid tumors of the small bowel?
- Uncommon - Cancers of neuroendocrine cells - Mostly arise in distal ileum or appendix
30
Treatment of carcinoid tumors of small bowel
- Resection if localized | - Control endocrine manifestations if metastatic (octreotide)
31
Where is colorectal cancer MC?
Western countries with high fat, low fiber diets
32
NSAIDs and colorectal cancer
NSAIDs may be protective against colorectal cancer
33
Genetic risks for colon cancer?
- Familial Adenomatous Polyposis (FAP) syndrome | - HNPCC or Lynch syndromes
34
Describe familial adenomatous polyposis
- Autosomal dominant - Development of hundreds to thousands of adenomatous polyps in colon - Symptoms usually by 25 yo - Increased risk of colon cancer
35
Initial treatment of patients with FAP or other familial syndromes?
Frequent colonoscopies
36
Definitive treatment of FAP/other familial syndromes?
Total colectomy
37
What can attenuate polyp formation?
NSAIDs and omega fatty acids
38
How is Lynch Syndrome or HNPCC diagnosed?
Bethesda Criteria
39
What are the Bethesda criteria?
Diagnose LS or HPNCC - 3 or more family members w/colon cancer (2 must be 1st degree relatives) - 2 successive generations w/colon cancer - 1 family member had colon cancer under 50 yo - NO FAP - 1 family member w/one of the extra-colonic cancers
40
What are LS and HNPCC characterized by?
Microsatellite instability on immunohistochemical staining
41
Colon cancers in HNPCC tend to occur:
Age 50 or less
42
Primary prevention of colorectal cancer:
- NSAIDs - High fiber, low fat diets - Ca, folic acid, Vit D? - Exercise? - HRT?
43
Secondary prevention of colorectal cancer:
Screening to start at 50 yo (or 10 years under the age your 1st degree relative was diagnosed)
44
Approved screening for colorectal cancer:
- Annual DRE w/FOB - Flexible sigmoidoscopy every 5 yrs - Colonoscopy every 10 yrs - Double contrast Ba enema every 5 yrs - CT colonography every 5 yrs
45
Drawback of flex sigmoidoscopy?
Can check bowel to approx 60 cm but 50% of colon cancers are R sided and cannot be reached by flex sig
46
Presenting symptoms of colorectal cancer
- Fe deficiency anemia in men or post-menopausal women - Stools positive for occult blood - Hematochezia - Change in bowel habits - Tenesmus
47
What is essential for a curative outcome of colorectal cancer?
Complete resection of all cancer and regional lymph nodes
48
What is the backbone of treatment for almost all GI cancers?
5-FU
49
What is cancer of the anus associated with?
- HPV - Genital warts and condyloma - MC in HIV
50
CDC recommendations for HPV vaccination?
Males 11-21 yo | Females 11-26 yo
51
Anal cancers are MC what type?
Squamous cell
52
How are anal cancers staged?
Unlike other GI cancers, it is staged by diameter of tumor (T3 is over 5 cm) and LN involvement
53
Preferred curative treatment for anal cancer?
Chemo (mitomycin C and 5FU) + RT | NOT surgery
54
Prognosis of pancreatic cancer
90% inoperable at time of diagnosis
55
What is Courvoisier's sign?
Palpable gallbladder (sign of pancreatic cancer)
56
What is Sister Mary Joseph Node?
Peritoneal carcinomatosis w/mets to umbilicus (sign of pancreatic cancer)
57
Where does hepatocellular carcinoma MC occur?
Sub-Saharan Africa | China and other parts of Asia (western)
58
What is hepatocellular carcinoma highly associated with?
Chronic hepatitis (HBV, HCV, ETOH)
59
Etiology of hepatocellular carcinoma in poorer countries
Contaminated food (Aflatoxin B1 from Aspergillus)
60
Treatment of hepatocellular carcinoma
- If localized, partial hepatectomy - If more generalized, transplant - Chemo-RT
61
What are pancreatic neuroendocrine cancers characterized by?
The hormones they secrete - Gastrinomas - VIPomas - Insulinomas - Glucagonomas
62
Describe MEN1
- Inherited syndrome of multiple endocrine neoplasms | - Pituitary adenomas, Parathyroid tumors, Pancreatic neuroendocrine tumors (PPP)
63
Describe MEN2
- Inherited syndrome | - Parathyroid tumors, Pheochromocytomas, Medullary thyroid cancer
64
Describe gastrointestinal stromal cell tumors (GIST)
Unique sarcomas of GI tract
65
MC form of GI sarcoma?
GIST
66
GISTs arise mostly in:
Stomach or small intestine
67
Treatment of GISTs
- Surgical resection (most important) | - 3 yrs of adjuvant PO Imatinib