Chapter 13: Primary Liver Cancer Flashcards

1
Q

primary liver cancer

A

hepatocellular carcinoma

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2
Q

leading cause of HCC

A

Hepatitis B Virus in places where hep B is endemic, and hepatitis C virus in North America.

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3
Q

surveillance using ____ and _____ shows an improvement in overall mortality from HCC

A

Alpha fetal protein Ultrasound

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4
Q

high risk populations in which HCC surveillance is cost-effective

A
  1. cirrhosis (regardless of the ethology) 2. certain HBV carriers - asian males >40 Asian females >50 Africans >30 - those with a family history of HCC
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5
Q

when is follow up after surveillance required?

A

if nodules are found on the surveillance US

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6
Q

T/F: you need a biopsy to diagnose HCC

A

false. HCC can be diagnosed with multi-detection computerized tomography (MDCT) or contrast MRI or CEUS. Also need AFP level. The higher the AFP, the poorer the prognosis. you require a biopsy only if these studies are negative.

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7
Q

Contrast enhanced studies take advantage of the ____ blood supply of the liver and that as nodules progress from a low-grade dysplastic nodule (L-DN) → high-grade dysplastic nodule (H-DN) → well differentiated HCC (WD-HCC) → moderately differentiated HCC (MD-HCC) they have ____ of their blood supply from neoplastic arteries with ____ blood supplied from the portal venous system (from GI)

A

Contrast enhanced studies take advantage of the dual blood supply of the liver and that as nodules progress from a low-grade dysplastic nodule (L-DN) → high-grade dysplastic nodule (H-DN) → well differentiated HCC (WD-HCC) → moderately differentiated HCC (MD-HCC) they have more of their blood supply from neoplastic arteries with less blood supplied from the portal venous system

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8
Q

Explain the portal venous washout effect

A

the contrast from the bowel usually travels to the liver through the portal vein (80% of the blood supply of the normal liver), but as the HCC has little of its blood supply from the portal vein and the arterial contrast has now left the lesion, it appears darker than the surrounding liver.

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9
Q

difference in portal space as the progression of HCC progresses

A

there’s less portal space and more neoplastic artery.

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10
Q

what factors does the barcelona clinic liver cancer staging system use to classify tumor stage

A
  • tumor burden
  • eastern cooperative oncology group performance satus
  • liver function via Child Pugh class.
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11
Q

aspects of child pugh classification

A

BCLC 0 & A (Very Early & Early Stage)
 5 year survival of 70% can be seen in patients carefully selected for curative options
of resection, radiofrequency ablation (RFA) or liver transplant (LT)
o BCLC B (Intermediate Stage)
 TACE increases median survival from 16 to 20 months
 TACE with drug eluting beads (DEB-TACE) can achieve median survival of 4 years

BCLC C (Advanced Stage)
 Sorafenib increases survival from 8 to 11 months o BCLC D (End Stage)
 Survival is < 3 months
 Patients with Child Pugh class C cirrhosis are end-stage unless LT candidates

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12
Q

curative and palliative treatment options

A

curative: sugical resection, RFablation, Percutaneous ethanol injection, liver transplantation in patients scoring 0 and A BCLC

Palliative treatment options: TACE, Sorafenib, levatinib, regorafenib, cabozatinib (chemotherapeutics).

In BCLC B, TACE increases median survival from 16 to 20 months. IN BCLC C, sorafenib increases survival from 8-11 months. In BCLC D, endstage, survival is less than three months unless they’re LT candidates.

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13
Q

rare liver cancer whose incident rate is increasing

A

intrahepatic cholangiocarcinoma

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14
Q

risk factors

A

Risk factors
o Cirrhosis
o Chronic viral hepatitis
o Primary sclerosing cholangitis
o Alcohol abuse
o Diabetes
o Obesity

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15
Q

surveillance of iCCA

A

it’s controversial, but carbohydrate antigen CA19-19 and US surveillance should be done in cirrhotics

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16
Q

diagnosing iCCA

A

MRI or CT shows liver mass with arterial phase enhancement. CEUS can show early and rapid washout. PET may be able to demonstrate lymph node involvement or metastases.

17
Q

In pts with resectable iccA (stage I and II), what’s the survival?

A

With curative resection, 5 year survival of 40% can be achieved but this falls to only 20% if
metastatic lymph nodes or vascular invasion are found at surgery

18
Q

in two thirds of patients (III and IV), iCCA is unresectable. what are some options?

A

if intra-heaptic disease, TACE can be offered but outcomes are worse than with HCC. Median survival is 15 months.

if extra-hepatic disease, chemotherapy with gemcitabine and cisplatin can be offered by median survival is typically <1 year.