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427
What microwave
ablation technique
is utilized for larger
tumors or those with
insufficient margins?
Synchronous ablation utilizing multiple
overlapping probes
How are ablation
patients typically
monitored post-
procedurally?
Monitored for pain and discharged with
pain medications.
If necessary, the patient may be admitted
overnight for pain control.
What medications
may be given prior to
TACE?
Variable. Some use a combination of
antiemetics, steroids, diphenhydramine,
and/or antibiotics.
When are
preprocedural
prophylactic
antibiotics indicated
for TACE?
Controversial. Some prescribe antibiotics
both 2–3days before and for 2–3weeks
following the procedure in patients
with increased risk of developing a liver
abscess (prior biliary interventions).
What vessel should
be interrogated
after aortography to
assess for accessory
or replaced hepatic
arteries?
SMA
What vessels
are commonly
interrogated, and
what are their
common injection
rates for hepatic
arterial interventions?
Aorta: 15–20mL/s for 30–40mL
SMA: 3–5mL/s for 12–30mL
Celiac: 3–4mL/s for 12–15mL
Common hepatic artery (CHA): 3mL/s
for 12mL
Gastroduodenal artery (GDA): 2mL/s
for 8mL
Proper hepatic: 3mL/s for 12mL
Left hepatic: 2mL/s for 8mL
Right hepatic: 2mL/s for 10–12mL
Phrenics: 1–2mL/s for 4–6mL
(continued)
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428
Once the hepatic
tumoral supply is
identified, what
maneuver is necessary
prior to delivery
of chemoembolic
emulsion?
A microcatheter (2–2.8 Fr) should
be used to obtain selective access for
segmental/subsegmental treatment.
How should the
patient be managed
immediately following
TACE?
Aggressive IV hydration, pain control,
such as with patient-controlled analgesia
(PCA), and antiemetics
How is imaging
response to TACE
monitored?
Contrast-enhanced CT or MRI~4weeks
after the procedure.
If there is no residual viable disease,
follow-up imaging should be performed
every 2–3months.
Which medications
should be
administered for
TARE?
PPI or H2 blocker 1week prior and for
4weeks following procedure
Nausea medication such as ondansetron
day of procedure
+/− steroids for postembolization
syndrome
+/− empirical antibiotics for biliary tract
infection
+/− oral analgesics
What is the dose
of 99mTc-MAA
delivered during the
mapping study?
Approximately 4–5mCi
Why is it essential to
calculate “lung shunt
fraction?”
30Gy delivered per session or 50Gy
cumulatively to the lungs has been shown
to induce radiation pneumonitis.
S. I. Stein
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429
What are the dose
reduction parameters
for patients with
lung shunting
demonstrated on
mapping study?
< 10% → no dose reduction.
10–15% → 20% dose reduction.
15–20% → 40% dose reduction.
> 20% → radioembolization is
contraindicated (with the caveat that it
may be performed in rare cases that total
absolute dose to the lung is less than
30Gy in a single session or 50Gy over
multiple sessions).
What imaging can
be performed to
document Y-90
deposition in tumoral
tissue?
Bremsstrahlung SPECT scan within 24h
of TARE
Newer modality time-of flight PET-CT
Complications
How are patients protected
from ablation of sensitive
nontarget tissue?
Hydrodissection with 5% dextrose
or sterile water can create a plane
between the ablation zone and
nontarget tissue.
What is the risk of tumor
seeding from RFA?
0.2–2.8% with risk factors including
high AFP, undifferentiated HCC,
subcapsular lesions, and multiple
needle insertions
Which patients are most
at risk for liver abscess
following liver-directed
therapy?
Prior biliary intervention
What is postembolization
syndrome?
Fever, abdominal pain, nausea, and
vomiting following an embolization
procedure
What is a commonly
utilized intraprocedural
practice to control pain
from visceral embolization?
Administer intra-arterial
lidocaine prior to delivery of
the chemoembolic emulsion and
between aliquots.
(continued)
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430
What potential life-
threating complications
exist from administering
too much ethiodized oil in
TACE?
Pulmonary embolism from
hepatovenous shunting to the lungs
and liver failure
How does the side effect
profile of TARE compare
to TACE?
TARE patients also may develop
constitutional symptoms including
fatigue, abdominal pain, and nausea.
However, symptoms are usually not
as severe or immediate but can be
prolonged.
What are the complications
of TARE?
Radiation pneumonitis,
radioembolization-induced liver
disease (REILD), liver toxicity, GI
ulceration, gastritis, skin irritation,
and cholecystitis
Where should TARE be
performed relative to the
cystic artery?
Distal to the cystic artery
How does REILD present
and how is it managed?
Can present up to several months
following TARE
Laboratory: elevated bilirubin and
decreased albumin
Clinical: ascites
Imaging: hepatic perfusion
abnormalities (veno-occlusive
disease)
Treatment: depends on severity,
may include diuretics, high-dose
steroids, sustained low-dose
heparin, ursodeoxycholic acid, and
pentoxifylline
What measures are taken
to avoid REILD when
performing bilobar whole
liver TARE or when
prescribed activity is high?
Dose reduction strategies or
sequential sessions/fractionation
to each lobe separated by 1-month
dosing to single lobe
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431
How are patients
protected from “nontarget
embolization” in TARE?
Prophylactic coiling or gel foam
embolization of potential nontarget
arterial branches
Landmark Research
Ablation
Chen M-S, Li J-Q, Zheng Y, etal. A prospective randomized
trial comparing percutaneous local ablative therapy and par-
tial hepatectomy for small hepatocellular carcinoma. Ann
Surg. 2006;243(3):321–8.
• RCT comparing percutaneous RFA with partial hepatec-
tomy for early solitary HCC≤5cm.
• Ablation and resection for early HCC had similar 1-, 2-, 3-,
and 4-year survival rates.
• Resection had statistically significant increase in complica-
tions related to surgery, longer hospital stay, and increased
postoperative stay.
Loriaud A, Denys A, Seror O, etal. Hepatocellular carci-
noma abutting large vessels: comparison of four percutane-
ous ablation systems. Int J Hyperthermia. 2018;34(8):1171–8.
• RCT in patients with BCLC stage 0 and A with perivascu-
lar HCC comparing monopolar RFA, cluster RFA, multi-
bipolar RFA, and microwave ablation.
• Primary endpoint: overall long-term progression.
• Multi-bipolar RFA and cluster RFA provided better local
tumor control than microwave ablation or monopolar
RFA.
Conventional TACE
Lo C-M, Ngan H, Tso W-K, Liu C-L, Lam C-M, Poon RT-P,
et al. Randomized controlled trial of transarterial lipiodol
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432
chemoembolization for unresectable hepatocellular carci-
noma. Hepatology. 2002;35(5):1164–71.
• TACE vs. symptomatic treatment for unresectable HCC in
Asian patients
• TACE with improved overall survival at 1, 2, and 3years
Llovet JM, Real MI, Montaña X, etal. Arterial embolisa-
tion or chemoembolisation versus symptomatic treatment in
patients with unresectable hepatocellular carcinoma: a ran-
domised controlled trial. Lancet. 2002;359(9319):1734–9.
• TACE vs. bland embolization vs. symptomatic treatment
for unresectable intermediate stage HCC in Caucasian
patients.
• The study was stopped due to consistent results showing
improved 1-, 2-, and 3-year survival of chemoembolization
patients.
• TACE group showed lower rates of vascular invasion and
lowest rate of death due to tumor progression, but the
study stopped prior to establishing improved effectiveness
compared to bland embolization.
DEB-TACE
Lammer J, Malagari K, Vogl T, etal. Prospective randomized
study of doxorubicin-eluting-bead embolization in the treat-
ment of hepatocellular carcinoma: results of the PRECISION
V study. Cardiovasc Intervent Radiol. 2010;33(1):41–52.
• Multicenter RCT with 1200 patients randomized to con-
ventional TACE vs. drug-eluting bead treatment of HCC,
with primary outcome of tumor response at 6months.
• Demonstrated safety of DEB-TACE, unable to demon-
strate superiority of DEB-TACE to conventional TACE.
• Subgroup analysis showed DEB-TACE with improved
response in more advanced disease (CP B, ECOG 1) com-
pared to conventional TACE.
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433
• DEB-TACE with improved tolerability and decreased
serious liver toxicity overall.
Lencioni R, Llovet JM, Han G, Tak WY, Yang J, Guglielmi
A, etal. Sorafenib or placebo plus TACE with doxorubicin-
eluting beads for intermediate stage HCC: the SPACE trial. J
Hepatol. 2016;64(5):1090–8.
• RCT comparing DEB-TACE alone vs. DEB-TACE +
sorafenib for intermediate stage HCC.
• Did not establish significant improvements in clinical out-
comes for combination group as opposed to DEB-TACE
alone.
Bland Embolization
Brown KT, Do RK, Gonen M, et al. Randomized trial of
hepatic artery embolization for hepatocellular carcinoma
using doxorubicin-eluting microspheres compared with
embolization with microspheres alone. J Clin Oncol.
2016;34(17):2046–53.
• Single-center RCT comparing bland embolization to
DEB-TACE for the treatment of HCC.
• Included BCLC A, B, and C patients in both groups
• No difference in imaging response, progression-free sur-
vival, or overall survival between the two groups
Transarterial Radioembolization
Salem R, Gordon AC, Mouli S, etal. Y90 radioembolization
significantly prolongs time to progression compared with
chemoembolization in patients with hepatocellular carci-
noma. Gastroenterology. 2016;151(6):1155–63.
• RCT conventional TACE vs. TARE for BCLC A and B
patients.
• Primary outcome: time to progression.
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434
• TARE had a significantly longer time to progression
(>26 months) than conventional TACE (6.8 months).
Longer time to progression did not translate to increased
overall survival.
Lewandowski RJ, Gabr A, Abouchaleh N, etal. Radiation
segmentectomy: potential curative therapy for early hepato-
cellular carcinoma. Radiology. 2018;287(3):1050–8.
• Retrospective cohort study of BCLC stage 0 and A
patients at single center with solitary HCC≤5cm treated
with radiation segmentectomy (>190Gy ablative dose).
• Median overall survival, 6.7 years; time to progression,
2.4years.
• Response rates, tumor control, and survival comparable to
other “curative” therapies such as thermal ablation, partial
hepatectomy, and transplantation in early stage HCC.
Wasan HS, Gibbs P, Sharma NK, et al. First-line selective
internal radiotherapy plus chemotherapy versus chemother-
apy alone in patients with liver metastases from colorectal
cancer (FOXFIRE, SIRFLOX, and FOXFIRE-Global): a
combined analysis of three multicentre, randomised, phase 3
trials. Lancet Oncol. 2017;18(9):1159–71.
• Analyzed data from three trials to assess chemotherapy
alone vs. chemotherapy + TARE with resin microspheres
as first-line therapy for patients with liver-only colorectal
cancer metastases
• Found that adding TARE improved liver-specific progres-
sion and radiological response, but did not improve overall
or progression-free survival
Vilgrain V, Pereira H, Assenat E, etal. Efficacy and safety
of selective internal radiotherapy with yttrium-90 resin
microspheres compared with sorafenib inlocally advanced
and inoperable hepatocellular carcinoma (SARAH): an
open-label randomised controlled phase 3 trial. Lancet
Oncol. 2017;18(12):1624–36.
• Multicenter RCT in France comparing the use of sorafenib
vs. TARE for patients with locally advanced stage (BCLC
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435
stage C) or intermediate stage (BCLC stage B failing
TACE) HCC.
• Primary endpoint: overall survival, which did not differ
between the two groups.
• TARE patients had improved QOL, improved tumor
response, and decreased adverse events (sorafenib can
have many toxic side effects).
Chow PKH, Gandhi M, Tan S-B, etal. SIRveNIB: selective
internal radiation therapy versus sorafenib in Asia-Pacific
patients with hepatocellular carcinoma. J Clin Oncol.
2018;36(19):1913–21.
• Multicenter RCT in comparing the use of sorafenib vs.
TARE for patients with locally advanced (BCLC stage B
or C) HCC.
• Primary endpoint: overall survival, which did not differ
between groups.
• TARE patients had fewer grade ≥ 3 adverse events than
sorafenib; TARE patients had better tumor response rate.
• Key differences from SARAH trial (above): Single TARE
(vs. SARAH with repeat TARE allowed), lower bilirubin
level threshold (32 mmol/L vs. <=50 SARAH), lower
proportion of BCLC C disease, and better survival in
patients with BCLC C disease treated with TARE in
SIRveNIB vs. SARAH.
Common Questions
What is the goal temperature of
RFA?
60–100°C (above 100°C
is less effective due to
charring).
What is the primary model utilized
to calculate activity for delivery of
Y-90 resin microspheres?
Body surface area (BSA)
model
(continued)
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436
What is the primary model utilized
to calculate activity for delivery of
Y-90 glass microspheres?
Medical internal radiation
dose (MIRD)
How long is the patient “radioactive”
after TARE and what measures
should be taken?
Y-90 has a 64-h half-life.
Patients should avoid close
contact with pregnant
women and children for
3days.
What is the typical surface radiation
dose from the patient after TARE?
< 1 mrem/h.
What is the goal future liver remnant
(FLR) before surgical resection in
patients with cirrhosis or chronic
hepatitis?
≥ 40% of the preoperative
liver volume
What is portal vein embolization
(PVE)?
Technique utilized to cause
compensatory hypertrophy
in the FLR.
PVE may increase FLR
by 30%.
Takes 3–4weeks to induce
hypertrophy.
What is radiation lobectomy? Delivery of Y-90in a lobar
fashion
Similar to PVE, causes
compensatory hypertrophy
to the contralateral lobe
prior to resection
Can take longer than PVE
to induce hypertrophy,
but has the advantage of
controlling the tumor(s)
What liver-directed therapies can be
used to target early HCC?
Depending on liver
transplantation candidacy
and location, thermal
ablation and radiation
segmentectomy can be
considered.
S. I. Stein
https://t.me/med1917
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