Hepatocellular carcinoma Flashcards

1
Q

Variant of HCC more common in women and occurring at younger age

A

fibrolamellar variant

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2
Q

presentation

A
  • typically asymptomatic

- Advanced stage → upper abdominal pain, weight loss, generalized weakness, anorexia or early satiety, emesis

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3
Q

Other things causing AFP elevation

A

1) chronic liver disease (acute or chronic viral hepatitis)
2) pregnancy
3) germ cell and non germ cell tumors

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4
Q

purpose of Child-Pugh classfication

A

classifies severity of liver disease

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5
Q

surgical therapies available for HCC treatment

A

Surgical resection (otpimal)

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6
Q

patients eligible for surgical resection

A

1) solitary HCC
2) confined to liver
3) no evidence of invasion into hepatic vasculature
4) no portal hypertension
5) preserved hepatic function (bili<1)

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7
Q

Locoregional therapies for HCC

A

1) Radiofrequency ablation
2) Transarterial chemoembolization (TACE)
3) External beam radiation
4) Radioembolization (y90)

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8
Q

management of patients with localized disease who aren’t surgery or transplant eligible

A

Locoregional therapies (preferred by NCCN guidelines)

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9
Q

targeted therapies for HCC?

A

several studies have shown a role for targeting EGFR/EGF (HER1), VEGF, and MEK/ERK pathways

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10
Q

classic enhancement pattern of HCC on imaging

A

arterial: increased
venous: decreased
delayed: persistent washout

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11
Q

What is Y90 for HCC?

A
  • Radioembolization
    Radioembolization is a minimally invasive procedure that combines embolization and radiation therapy to treat liver cancer. Tiny glass or resin beads filled with the radioactive isotope yttrium Y-90 are placed inside the blood vessels that feed a tumor.
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12
Q

most common sites of mets

A
  • lung
  • intra-abdominal lymph nodes
  • bone
  • adrenal gland
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13
Q

AFP threshold triggering evaluation for HCC

A

20

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14
Q

Imaging criteria for HCC diagnosis in high risk patient

A

1) non-rim hyperenhancement in the arterial phase + fulfills size criteria given

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15
Q

First-line systemic therapy for Child-Pugh Class A

A

Atezolizumab + bevacizumab

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16
Q

First line for metastatic HCC (Child Pugh Class A)

A

Atezo + bev

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17
Q

Other recommended regimens for metastatic HCC

A

1) sorafenib

2) lenvatinib

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18
Q

Sorafenib MOA

A

Targets RAF/MEK/ERK

And VEGF/PDGFR

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19
Q

Second line therapies for HCC

A

1) regorafenib
2) cabozantinib
3) ramucirumab
4) lenvatinib
5) sorafenib
6) ipi-nivo

20
Q

Adequate liver remnant s/p surgery in patient with healthy liver (by percentage)

A

20%

21
Q

Transplant eligibility criteria

A

1) ≤5 cm in diameter OR up to three separate lesions, none of which is larger than 3 cm
2) **no gross vascular invasion
3) no regional nodal or distant metastases (the Milan criteria
4) **
no portal vein thrombosis

22
Q

Local therapies for HCC + categories

A

1) Ablative — RFA, Cryoablation, Percutaneous EtOH injection
2) Arterial-directed therapies —
OR chemoembolization (TACE or drug-eluting beads)
3) SBRT

23
Q

Contraindications to chemoembolization

A
  • Child Pugh C
  • portal vein thrombosis (obstructs chemo)
  • bilirubin >3
24
Q

How does chemoembolization work?

A
  • chemotherapy is administered into the hepatic artery
25
Q

Typical regimen for chemoembolization

A

doxorubicin-based

26
Q

Name of criteria used to determine if patient is eligible for transplant

A

Milan/UNOS criteria

27
Q

Radiographic criteria for diagnosis of HCC

A
  • hyperenhancement in arterial phase
  • venous or delayed phase washout appearance
  • enhancing capsule appearance
28
Q

Only systemic treatment option for patients with Child-Pugh Class B disease

A

Sorafenib (confirm this)

29
Q

Preferred immunotherapy in second line

A

Ipi/nivo (pembro is category 2B)

30
Q

Algorithm for managing localized disease

A

Determine if

1) Surgical candidate
2) IF not surgical candidate, consider whether transplant candidate
3) IF not surgical or transplant candidate, evaluate if eligible for local therapies

31
Q

What are the ablative therapies

A
  • radiofrequency (RFA)
  • cryoablation
  • percutaneous alcohol injection (confirm)
  • microwave
32
Q

what are the arterially directed therapies?

A
  • bland transarterial embolization
  • chemoembolization (TACE)
  • radioembolization (Y-90 microspheres)
33
Q

Child Pugh C management

A

Hospice, systemic therapy never recommended

34
Q

alternative to Child Pugh C that has better interobserver reliability

A

ALBI score

35
Q

primary problem with child pugh score

A

Low interrater reliability given variability in grading encephalopathy and ascites

36
Q

best option for a cirrhotic

A

transplant (fix cirrhosis and HCC)

37
Q

why surgical resection is much less common in the US

A

cirrhotics in US have EtOH or NASH, as opposed to hep b. Thus, they have much lower hepatic reserve. Less than 5% are eligible for surgery in the US! Typicallly only realistic options for patients with hep b cirrhosis.

38
Q

Drug that doesn’t work for NASH cirrhosis

A

immunotherapy (TKI’s better first line, possibly followed by immunotherapy (TKIs increase immunogenicity))

39
Q

Ipi, Nivo formulation approved for second line

A

Nivo1 +/- Ipi3, thus more toxic

40
Q

evidence for adjuvant treatment

A

There is no robust data that suggest a benefit of adjuvant therapy following resection

41
Q

LI-RADS 4, biopsy?

A

Typically don’t

42
Q

First line for immunotherapy ineligible

A

Lenvatinib (highest response rates)

43
Q

When is regorafenib indicated second line?

A

Only for patients who tolerated sorafenib frontline

44
Q

Preferred second line

A

Cabozantinib (best tolerated and broad eligibility vs. other second line studies only approved for patients who tolerated frontline sorafenib, etc)

45
Q

Term for criteria for transplantation

A

Barcelona Clinic Liver Cancer (BCLC) OR Milan

46
Q

When is TACE used

A

Not transplant or surgical candidate and LARGE tumors (greater than 3cm)