Colorectal, Esophageal and Gastric Cancer Flashcards

1
Q

Esophageal Cancer
Etiology
Risk Factors

A

adenocarcinomas: more common in the US
squamous cell carcinoma is the majority of cases worldwide

Risk Factors for …

Adenocarcinoma
- 60% have evidence of barrets esophagus
- long-standing GERD
- tobacco use
- obesity
- MSR I, ASCCI & CTHRCI gene mutations

Squamous Cell Carcinoma
- alcohol & tobacco use (highest risk factors)
- dietary factors
- alkaline/lye ingestions
- tylosis palmaris and plantaris (chrom. 17 deletion)

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2
Q

Barrett’s Esophagus
etiology
risk factors
patho: where does this occur within the esophagus & Diagnosis

A

long-standing GERD: exposure to the stomach acid leads to change from normal squamous epithelium to gastric columnar cells

  • increased risk for the developement of esophageal cancer by 30-60%

Risk Factors for Barrett’s
- chronic GERD
- hiatial hernia
- age > 50
- male, white
- obese
- smoker
- cancer of esophagus in family 1st degree relative
- some assocation with h pylori (low)

Diagnosis
- normally: there is a Z line: where the cells go from columnar to squamous of the esophagus: Z line is at the GEJ
- if columnar epithelium is > 1 cm of the distal esophagus AND biposy shows metaplasia = barretts

low grade dysplais: 1% increased risk
high grade dysplasia: 5% increased risk

if concurrent esophagitis: need to repeat the EGD in 3 months to recheck for barretts or adenocarcinomas

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3
Q

Screening Recommendations for Esophageal Cancer in those with Barrett’s

Treatments for Barrett’s (if not PPI)

A

screenign every 3 years if thye have nondysplasia Barrett’s
- if they have dysplsaia: more frequently

the earlier you catch teh adenocarcinoma, the better the outcome!

Barretts Treatment
- can do radiofrequency ablation: still need to screen for dysplasia (can comeback)

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4
Q

esophageal cancer
Symptoms

A

Symptoms
1. progressive dysphagia: (most common symptom)
- started with solids initially: now liquids too
- this is unfortunaltey a late manifestation of the disease

  1. Odynophagia/globus sensation (food is stuck feeling)
  2. anoerexia/weight loss
  3. worsening refulx
  4. nauseas
  5. GI bleed: an upper Gi bleed from the tumor itself (hematemeisis, melana)

oropharyngeal function is usually in tact

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5
Q

Esophageal Cancer
Work up
Histology and locations
Diagnosis

A

Work-up
Esophagogastrodudenoscopy (EGD) with ultrasound
- with a bioposy of the tumor
- US helps reveal the primary tumors size and if there is lymph node involvement

if need to elvaulated for mets…
- CT chest/abd/pelvis with IV contrast
- PET/CT can be used

Histology/Location of the Cancer
Squamous Cell Carcinoma
- will see squamous dysplasia
- loactsion: majority in the middle 1/3 of esophagus

Adenocarcinoma
- will see barrett’s first, or incomplete intestinal metaplasia on biopsy
- location: distal 1/3 of the esophagus MC at the GE junction

Classification of GEJ Tumors
Type 1: center of lesion 1-5 cm proximal to GE junction (esophageal cancer)
Type 2: 1 cm proximal to and 2 cm distal to teh GE junction (iffy zone)
Type 3: 2-5 cm distal to the GE junction (shows its really stomach cancer)

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6
Q

Esophageal Cancer: Staging
the basics

A

Staging: gives idea baout how far the cancer has spread from its original location; higher sprea = poor prognosis

in situ = cells are abnormal, high RISK for being cancerous

metastatic: cancer cells have spread from orgin to elsewhere

staging is done using the TNM system
T= Tumor
N = regional lymph nodes
M = metastisis
(ex. T2N1M0 is a TNM that gives you a “stage”)

the Stage guides treatment decisions and re-staging can occur through treatment

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7
Q

Esophageal Cancer: Treatment
general principles
- surgical resecetion when
- systemic therapy options (meds)

A

Generally for cancer, early finding = early treatmetn can be curative

Early = neoadjuvant chemo + surgical resection + post-op radiation

Advanced Stages: palliative treatment
- chemothearpy to slow the spread and imrpove symptoms

Surgical Ressection
1. if early stage (Tis or Tia): endoscopic surgery can be done
2. locoregional (stage 2-3 ot T4b): tradional surgery
- pt. recives pre-op chemo carboplatin/taxol + radiation
- transhiatal esophagectomy (connect stomach to upper part of esophagus and remove distal esophagus)

Systemic Thearpy: for Stage IV
1. first-line: platinum-based thearpy + fluropyrimidine backbone
- example: DCT (docetaxel, cisplatin, 5-FU)

  1. Ramucircumab + -taxel
  2. Immunotherapy with anti- PDL-I (if they have CA which expressed PDL-I) –> nivlumab + pembrolizumab
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8
Q

Complications of Esophageal Cancer

Liver Mets
Peritoneal Mets

A
  1. worsening dysphagia: can get worse while doing treatment, then gets better
    - can require a G or J tube for short term combat if needed
  2. metastatic disease: lymph, liver, lung, bone, adrenal glands and brain

Liver Metastitsis (normal function: mets effect)
- toxin removal : hepatic encephalopathy
- bilirubin: jaundice
- proteins: third-spacing, risk of bleeding and increased infection risk
- platelets: chronic thrombycytopenia
- glycogen storage: imparied glucose regulation

Peritoneal Metatstisis (poor prognosis)
peritoneum: lining of abdominal wall and cavitiy; mesintery: attaches the viseral organs to the peritoneum

  • ascites
  • pain
  • abd. distension
  • bowel obstruction: SBO
  • not able to get G or J tube because too risky of surgery

survival is better if caught early
avoid red meats, tobacco, alcohol, treat the GERD, use statins to avoid esophageal cancer

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9
Q

Gastric Cancer
types
risk factors

A

Types
- gastric adenocarcinoma (most common)
- gastrointestinal stromal tumors (nerve cell)
- carcinoid tumors (secreting things it should not be)
- lymphoma

more commonly found at the GE junction: proximal stomach

Risk Factors
- H pylori infection
- tobacco, alcohol
- obestiy
- GERD
- EBV
- radiation
- pernicious anemia
- exposures (coal/rubber)
- poor diet with cured/smoked foods, salts, low vit. c/a

Genetic Risk Factors
- 15% are familial in origin
- Lynch Syndrome
- Diffuse heredity Gastric Cancer (A-dom.) (gasterectomy at 40 to prevent CA)

others..
- li-fraumei
- polyposis (familial)
- juvenile polyposis
- peutz-jeghers syndrome

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10
Q

Gastric Cancer
Symptoms
Diagnositc Workup
Staging

A

unfortunately; usually diagnosed late

  • weight loss/anorexia
  • stomach pain
  • early satiety
  • GI bleed (upper GI)
  • ascites (later in disease when they present with this)

Diagnostic
- EGD with US & biopsy
- CT w/ IV contrast if needed to assess spread
- PET if needed

Staging
- TNM system: assessing the spread of disease based on histology, pathology and spread

biopsy
- polypoid: looks like a mushroom
- Fungating: necortic; eating the middle
- Ulcerated: infilterative
- Flat: younger pts, but high grade signet ring sign

Histology Lauren Histological Classification
1. Intestinal Type: columnar, gland-forming cells with irregular margins and ulcerations
2. Diffuse Type: Signet ring cells, with linitis plastica: rubber think wall (worse)

lots of pathological testing to determine the genetics which underlie the cancer cells to figure out how best to treat it

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11
Q

Gastric Cancer
Treatment

A

Stages I-III: locoregional disease
- subtotal gasterctomy preferred: part of stomach is removed
- may include neoadjuvant or adjuvcant chemotherapy
neoadjuvt: FLOT or FOLFOX or epirubicin/cicplatin/5-FU
adjuvcant: leucovorin + radiation OR cisplatin + radiation OR capecitabine + oxaliplatin

Stage IV (advanced)
- first line treatment: anti-PDL-I (pembrolizumab or nivolumab) if its PDL-I expressing
- seond line: platium based + fluropyrimidine backbone
- third line: VEGFR-2 monoclonal antibody (ramucirumab + paclitaxel)

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12
Q

Gastric Cancer
Complications and Prevention

A

Complications (cancer or teh treatment)
- occult GI bleeding (diffiuclt to treat)
- early satiety + N/V/reflux
- metastatic disease: to the liver, peritoneum and lungs

Prevention
- screen for h pylori!!!
- screenig for gastric cancer in high risk groups

High Risk
- gastric adenoma
- pernicious anemia
- gastric intestinal metaplasia
- familial polyposis
- lynch syndrome
- jeuvinile polyposis
- peutz-jeghers

earlier you catch it, the better off the pt. is

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13
Q

Colon Cancer
Etiology
Risk Factors
polyp type and size

A

3rd most common death in women, 2nd in men

Risk Factors
- high red meat diet
- alcohol use
- DM
- metabolic syndrome
- longstanding IBD : 25 years (more likely with pan-colitis)
- streptococcus bovis bacteremia
- familial polyposis
- lynch syndrome & heridiatray non-polyposis

asprin/NSAIDS can and may be protective

Etiology: begins as a polyp (various types)
Sessile polyps: flat
villous adenoma: pedunculated
tubulovillous adenoma: pedunculated
tubular adenoma: pedunculated

assessed by their shape, size, type of polyp, number and location

Size
- < 1.5 cm = low risk
- 1.5-2.5 = intermediate risk
- > 2.5 = high risk

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14
Q

Colon Cancer
Symptoms
Work-Up and Diagnosis

A

Symptoms
- Bleeding: (importatnt early symptom)
- a change in bowel habits (anythin that theyve noticed is different –> weeks/months)
- fecal urgency
- imcomplete bowel emptying
- pain (late symptom)

Location & Symptoms
- right colon: microcytic anemia
- Left colon: abdominal cramping, obstruction or performation
- rectosigmoid: hematochezia, tenesmus, stool pattern change

Diagnosis
- biopsy via colonoscopy = most sensitive and specific (over a sigmoidoscpy - doesnt got the whole colon)
- barium enema: apple core lesions
- CT with IV contrast + oral contrast for staging
- Carcinoembryonic antigen (CEA) = tumor marker to monitor treatment (NOT used to dx.)

Staging
- TNM system used here as well

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15
Q

Colon Cancer
Treatment

A

Resectable Disease
- colectomy with regional lymph node dissection

can do adjuvant therapy if…
1. T4 tumor
2. poor histology
3. lymphovascualr invasion
4. bowel obstruction
5. interdeterminate margins on colectomy

adjuvcant therapy: = 5-FU/leucorvorin, capecitabine, FOLFOX or CAPEOX

Metastatic Disease
- if liver mets only: can rescent the liver mets! good survival
- systemic therapy = 5-FU/leucorvorin, capecitabine, FOLFOX or CAPEOX
- progressive disease: MMR or MSI tumors = pembrolizumab or nivolumab (PDL-I) or ipilimumab +nivolumab

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16
Q

Colon Cancer
Complications

A
  • large bowel obstruction
  • GI bleeding
  • metastis disease liver, lungs and brain
17
Q

Colon Cancer Screening
- when to screen
- whos at increased risk
- whos at high risk

A

average risk individual: first screening should be at age 45!!!

Average risk: 45 years with no other risk factors
increased risk
- family has history of colorectal cancer or advnaced polyps
- you have had colorectal cancer or advanced polyps
- you have… ulcerative colitis or chrons

High Risk: YOU have…
- lynch syndrome
- polyposis syndrome

18
Q

Colon Cancer Screening
what test

family history specifics and when to screen

A

colonoscopy is best; longer time between

Colonscopy: rescreen in 10
sigmoidoscpy: 5 to 10
CT colonography: 5 years
DNA stool: 3 years
Guaiac based or fecal immunochemcia: 1 year

Family History:
- if 1st degree relative had colorectal cancer = you get age 40 or 10 years before they were diagnosed & resecreen 5 years later
- if 2nd or 3rd degree realtive had colorectal cancer = you get age 45 or before 45 if they ahd early onset & again 10 years
- if you 1st degree had polyp issue = you get age 40 or at same age they found out & again every 5 to 10 years

19
Q

Colon Cancer Screening
IBD pts.

A

IBD increases your risk for colon cancer –> screen 8 years after start of IBD symptoms

evern higher risk if family history of cancer or polyp condition

screnning done with IBD not acivte and with colonoscopy

20
Q

Polyps found on colonscopy
- when do you get it again?
- how are they removed

A

small pre-cancerous polyps
- lots? 1, 3 or 5 years
- few : like 1? 7-10 years

large pre-cancerous polyps
- pedunculate: 3 years
- flat: 1-3 years
- flat but risky: 6 months

Removal
- remove all you can enough that you can send it for testing

Types
- snare: for pedunculated polyps
- mucosal resection: large sessile polyps
- submuscosal resection: using disseting knife to get to submucosal

21
Q

Platinum based chemo
- names
- side effects
- high take aways

A

Platinum Based = cisplatin, carboplatin, oxaliplatin

  • neurotoxic
  • nephrotoxic
  • ototoxic (can be perminent)

Take Aways
- highly systemically tocxic
- side effects are dose related
- carboplatin is less toxic
- resistance is possibel

22
Q

Anti-Metabolite (Fluoropyrimidine based)
- names
- side effects
- big take aways

A

Atni-metabolite = 5-FU, capecitabine, flxuridine

side effects
- GI toxici
- mucositis (lesions in the mouth)
- neutropenia
- Hand-foot syndrome

Take Aways
- well tolerated
- individualize dosing

23
Q

Anti-microtubulin (taxane derivitives)

Names
Side Effects
Take aways

A

Names
- pacitaxel
- docetaxil
- carbazitxel

Side effects
- heptatotoxic
- neutropenia
- hypersensitivy
- fluid retention

Side Effect
- watch pulmonary toxicit (fluid retention) , Interstitial pneumonitis, capillary leak
- hypersensitivtiy reaction

24
Q

Topoisomerase I inhibitors
Names
SE
Take Aways

A

Names
- doxirubicin
- epirubicin
- topotecan
- irnotecan

Side Effects
- dirrahea
- bone marrow suppression
- cardiomyopathy
- tissue injury/necrosis (central line)

Take aways
- doxrubicin= significant cardiomyopathy effect– get TTE first and during

25
Q

Monocloncal antibody
name
SE

A

Trastuzumab (herceptin)

cardiomyopathy and infusion reaction

tumor must express HER2 for this to work

26
Q

Folinic Acid: chemo modulators
Names
SE
take away

A

leucovorin

side effect
- atopic derm
- stomatitis
- gi toxic

enhances the 5-FU effect