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Predominant occurrence with diseases:
Chronic liver disease and cirrhosis
Difference between First & Second type
single tumor spreads late in stage to other parts of live vs small nodules throughout the liver
Second type appears w/ cirrhosis, mainly US
Incidence
41260; has tripled since 1980
Trends lending to increased Incidence
Obesity, T2DM, Nonalcoholic fatty liver disease
Modifiable risk factors
obesity
High fat diet
NAFLD
Diabetes
Alcohol
Smoking
Exposure to chemical carcinogens
Anabolic steroids
Nonmodifiable risk factors
primary biliary cirrhosis
Nonalcoholic steatohepatitis
Hep B or C
Hemochromatosis
Wilson’s Disease
Parasitic infection
Male gender
Asian Americans and Pacific Highlanders
Prevention
Avoiding/treating hepatitis infections
Limit alcohol use
Limit smoking
Healthy weight
Limit exposure to carcinogenic chemicals
Treat diseases increasing HCC risk
Diagnosis
Angiography
US
Bone scan
Abdominal multiphasic CT
MRI
Alpha fetoprotein
Biopsy
Biopsy Considerations
if solid tumor, determined by size
Not required is lesion fulfills imaging criteria
Gross morphology
nodular = associated with cirrhosis
massive = noncirrhosis type
Diffuse = small distinct areas throughout liver
Staging Systems
Child-Pugh (cirrhosis)
Model for ESLD
Okuda
Localized tumor survival
30%
Advanced tumor survival
3%
Surgery Options
partial hepatectomy: potentially curative in early stage, Child-Pugh A (need some liver function)
Transplantation
Transplant considerations
potentially curative in early stage
May include bridge therapy - transarterial chemoembolization or thermal/radiofrequency ablation
Local-regional therapies
Ablation: RFA, Microwave, Cryo
Arterial Directed: transarterial bland embolization, TACE, yytrium-90 transarterial radioembolization (TARE), TACE w/ drug-eluting beads
Radiation
intensity modulated radiation
Stereotactic body radiation
Systemic Treatment
1st Line: Sorafenib
2nd Line: Regorafenib, Nivolumab (Child-Pugh A-B7 only)
Chemo only in trials