Y90 HCC Flashcards

(56 cards)

1
Q

Why is complete pathological necrosis important for HCC Y90

A
  • tumors with CPN had lower HCC recurrence rate than tumors with incomplete necrosis
  • CPN has lower HCC-related mortality, recurrence free survival, and longer time to recurrence

https://pubmed.ncbi.nlm.nih.gov/32749512/

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2
Q

Target dose per LEGACY trial for HCC segmental Y90 infusion

A

> 400 Gy

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3
Q

how many segments are in a radiation segmentectomy

A

2 segments or less

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4
Q

check list of vessels to watch for in MAA mapping

A
  1. GDA
  2. cystic
  3. Right gastric artery
  4. gastrohepatic trunk
  5. falciform
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5
Q

characteristic appearance of the cystic artery

A

inverted Y or “forked tongue” appearance

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6
Q

mesenteric angiography power injections times for

  1. proximal anatomical delineation
  2. parenchymal background
  3. venous outflow
A
  1. 0-2 seconds
  2. 2-10 seconds
  3. 10-20 seconds
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7
Q

tumor size and liver volume percentage radiation major hepatectomy is performed

A

Patients with HCC 5 cm or larger, greater than 60% of the total liver volume

https://learn.sirweb.org/pluginfile.php/61503/block_html/content/Feb%202024%20JVIR%20article.pdf

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8
Q

what is the Future liver remnant per Nontumor liver volume radiation major hepatectomy be performed

A

FLR/NTLV has to be greater than 30%

https://learn.sirweb.org/pluginfile.php/61503/block_html/content/Feb%202024%20JVIR%20article.pdf

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9
Q

according to the IFU for theraspheres, what is the maximum dose that is recommended to the total liver volume

A

150Gy per whole liver

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10
Q

what is the standard definition of major hepatectomy

A

resection of 4 or more liver segments

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11
Q

other than a FLR/NTLV of greater than 30%, what other criteria were listed for performing radiation major hepatectomy

A
  1. Child-Pugh Class A
  2. ECOG 0
  3. no vascular invasion
  4. less than 5 tumors
  5. no evidence of extrahepatic spread
  6. no tumor in the FLR
  7. estimated lung dose <30Gy while achieving >150Gy in the perfused volume

https://learn.sirweb.org/pluginfile.php/61503/block_html/content/Feb%202024%20JVIR%20article.pdf

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12
Q

lung dose threshold has to be less than what

A

less than 30 Gy

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13
Q

Epidemiology of liver cancer - how common is it worldwide and where does it rank in cancer-related deaths?

A

6th most common cancer worldwide
3rd leading cause of cancer related deaths world wide and in the US

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14
Q

what is the strongest risk factor for developing HCC

A

cirrhosis

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15
Q

what is the annual risk of developing HCC in patients with cirrhosis

A

around 2 %

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16
Q

what is the leading cause of HCC in the absence of cirrhosis

A

NAFLD - approximately 1/4 to 1/3 of NAFLD-related HCC occurs in the absence of cirrhosis

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17
Q

what beverage may be recommended for patients with chronic liver disease

A

Coffee (but with no additives)
At least one cup of coffee consumption is dose-dependently assocated with a significant reduction in HCC risk

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18
Q

what medications have a protective effect against HCC

A
  1. aspirin (43-60% reduction in HCC risk with aspirin use exceeding 5 years)
  2. statins (potential benefit from lipophilic statins but not hydrophilic statins)
  3. metformin (conflicting data)

https://journals.lww.com/hep/fulltext/2023/12000/aasld_practice_guidance_on_prevention,_diagnosis,.27.aspx

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19
Q

should statins be avoided in patients with chronic liver disease

A

No

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20
Q

does HCC surveillance have any benefit in patients with Child-Turcotte-Pugh score C

A

No, unless they are a transplant candidate

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21
Q

what is the difference between MASH and NAFLD

A

MASH is a more severe form of NAFLD. It includes all the features of NAFLD but with additional inflammation and liver cell injury.

MASH has a higher risk of progressing to advanced liver diseases compared to simple NAFLD.

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22
Q

What stage of fibrosis is considered cirrhosis

A

Stage 4

Stages of Liver Fibrosis
F0: No fibrosis.
F1: Mild fibrosis with portal expansion.
F2: Moderate fibrosis with more extensive portal expansion and some bridging fibrosis.
F3: Severe fibrosis with bridging fibrosis but no cirrhosis.
F4: Cirrhosis. This stage is characterized by extensive fibrosis with the formation of regenerative nodules and significant disruption of liver architecture

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23
Q

what surveillance test(s) do the AASLD recommend

A

combo of US and AFP
https://journals.lww.com/hep/fulltext/2023/12000/aasld_practice_guidance_on_prevention,_diagnosis,.27.aspx

24
Q

GALAD panel sensitivity range for early HCC detection

A

60-80% sensitivity
82% specificity

Berhane S, Toyoda H, Tada T, Kumada T, Kagebayashi C, Satomura S, et al. Role of the GALAD and BALAD-2 Serologic Models in Diagnosis of Hepatocellular Carcinoma and Prediction of Survival in Patients. Clin Gastroenterol Hepatol. 2016;14:875–886 e876.

Marrero JA, Marsh TL, Parikh ND, Roberts LR, Schwartz ME, Nguyen MH, et al. GALAD score improves early detection of HCC prior to the diagnosis of HCC: A phase 3 biomarker validation study. Abstract #138. Hepatology. 2021;74:92A.

25
GALAD panel composition
gender, age, AFP-L3, AFP, DCP
26
how often should HCC surveillance be performed
every 6 months *this recommendation was initially based on HCC tumor doubling time
27
AFP 20 ng/mL sensitivity and specificity
sensitivity around 60% specificity around 90%
28
AASLD next step if screening US for HCC shows a subcentimeter lesion
Repeat US and AFP in 3-6 months
29
AASLD next step if screening US for HCC shows a 1 cm or greater lesion
further imaging with multiphasic CT or MRI
30
percentage of HCC that can have normal AFP levels
over 40% Arif D, Mettler T, Adeyi OA. Mimics of hepatocellular carcinoma: a review and an approach to avoiding histopathological diagnostic missteps. Hum Pathol. 2021;112:116–27
31
other tumors that may have elevated AFP levels
intrahepatic cholangiocarcinoma, gastric cancer, and germ cell tumors
32
is the diagnosis of HCC based on elevated AFP alone valid
no - need imaging or biopsy if imaging non-characteristic
33
who does LI-RADS not apply to
patients without cirrhosis or at-risk chronic HBV infection
34
when is a CT chest recommended for patients with HCC
when tumor is 2 cm or greater in size to assess for lung mets *all patients beyond stage 0 of the BCLC criteria
35
when is staging with CT pelvis and Technetium-99m Bone scan recommended for HCC
1. patients with AFP greater than 1000 ng/mL 2. macrovascular invasion 3. multifocal bilobar disease
36
factors to consider for surgical resection of HCC
1. tumor number 2. anatomic location 3. presence of vascular invasion 4. anticipated FLR 5. liver function 6. presence of clinically significant portal hypertension
37
FLR needed with cirrhosis vs. without
40% with cirrhosis 30% without cirrhosis
38
how is clinically significant portal hypertension defined
HVPG greater than 10
39
what are surrogates for CSPH when not using HVPG
presence of ascites and varices, and platelet count <100k
40
risk of HCC recurrence following surgical resection
50-70% at 5 years
40
high risk features for HCC resection patients
1. tumor size greater than 5 cm 2. more than 3 tumors 3. micro/macrovascular invasion 4. poor tumor differentiation
40
what is the recommended treatment for localized HCC in the absence of underlying cirrhosis
surgical resection
40
when should surgical resection be considered in patients with cirrhosis
when there is 1. limited tumor burden 2. well-compensated cirrhosis 3. no CSPH 4. adequate FLR
41
what type of therapy is recommended for post-resection HCC patient with high risk of recurrence
adjuvant treatment with atezo and Bev (IMbrave 050)
42
HCC recurrence rate after transplantation vs. resection
transplantation: 10% resection: 50-60% AASLD paper: file:///C:/Users/George/Downloads/aasld_practice_guidance_on_prevention,_diagnosis,.27%20(2).pdf
43
what is the criteria for HCC transplant known as
the Milan criteria
44
what is used to rank liver transplant candidates
MELD-Na
45
what type of immune checkpoint inhibitors are there for HCC treatment
1. anti-PD-1 2. anti-PD-L1
46
what are the Anti-PD-1 immune checkpoint inhibitors
nivolumab (Opdivo) and pembrolizumab (Keytruda)
47
what are the anti-PD-L1 immune checkpoint inhibitors
Atezolizumab (Tecentriq) Avelumab (Bavencio) Durvalumab (Imfinzi)
48
What risk to immune check point inhibitors carry in cases for potential liver transplant
Immune checkpoint inhibitors (ICIs) may increase risk of rejection and graft loss,
49
If a patient was on an immune checkpoint inhibitor for liver transplant bridging, how long should they be off of them prior to transplant
If patients receive ICIs prior to LT, we recommend discontinuation of these agents at least 3 months prior to LT - per AASLD guidelines
50
recurrence rate of HCC post liver transplant
Even with adherence to the Milan criteria, HCC recurs post-LT in 10%–15%
51
the two most common sites for post liver transplant HCC recurrence
the lung (40%) and the liver (33%)
52
HCC ablation has a similar survival for tumors of what size
2 cm or less
53
what did the IMbrave 050 study results demonstrate
IMbrave 050 phase III RCT demonstrated superior recurrence-free survival using atezolizumab plus bevacizumab in the adjuvant setting for HCC patients at high-risk of recurrence after surgical resection or local ablation. High-risk features for patients undergoing ablation in this trial included tumor size >2 cm but ≤5 cm and multifocal HCC.