Journal of Hepatocellular Carcinoma,
Journal Year:
2023,
Volume and Issue:
Volume 10, P. 2133 - 2145
Published: Nov. 30, 2023
To
assess
the
clinical
value
of
pretherapeutic
systemic
inflammation
score
(SIS)
in
predicting
prognosis
hepatocellular
carcinoma
(HCC)
after
hepatic
arterial
infusion
chemotherapy
(HAIC).From
February
2016
to
April
2021,
415
advanced
HCC
patients
who
underwent
HAIC
at
Sun
Yat-sen
University
Cancer
Center
were
randomly
divided
into
training
(n
=
277)
and
validation
cohorts
138)
analyzed.
The
aspartate
aminotransferase-alanine
aminotransferase
ratio
(AAR),
lymphocyte
×
albumin
(L
A),
neutrophil
monocyte
(N
M)
used
construct
SIS
based
on
a
multivariate
Cox
analysis
cohort.
A
nomogram
consisting
was
created
evaluated
by
calibration
plot,
areas
under
receiver
operating
characteristic
(AUC)
curve,
decision
curve
(DCA).Univariate
analyses
revealed
that
an
independent
predictor
OS.
high
associated
with
large
tumor
size
(P
<
0.05),
multiple
lesions
0.01),
AFP
level
extrahepatic
metastasis
BCLC
stage
0.01).
Kaplan-Meier
showed
had
shorter
OS
than
those
low
both
non-PD
(p
0.015)
PD
group
0.023).
plots
good
concordance
between
nomogram's
prediction
actual
observations
cohorts.
In
cohort,
AUCs
2-year
3-year
survival
rates
0.749
0.739,
respectively;
they
0.760
0.681,
respectively.
Based
AUC
DCA,
better
predictive
ability
other
predictors.The
is
potential
prognostic
for
undergoing
HAIC.
Discover Oncology,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: July 3, 2024
Abstract
Liver
cancer
is
the
sixth
most
commonly
diagnosed
and
third
leading
cause
of
death
in
world,
hepatocellular
carcinoma
(HCC)
common
form
liver
cancer.
More
than
half
HCC
patients
are
at
an
advanced
stage
often
require
systemic
therapy.
Dysregulation
activity
receptor
tyrosine
kinases
(RTKs)
involved
development
progress
HCC,
RTKs
therefore
potential
targets
for
therapy
(aHCC).
Currently,
a
total
six
small
molecule
kinase
inhibitors
(TKIs)
have
been
approved
aHCC,
including
first-line
sorafenib,
lenvatinib,
donafenib,
second-line
regorafenib,
cabozantinib,
apatinib.
These
TKIs
improved
survival,
which
associated
with
disease
stage,
etiology,
function,
tumor
burden,
baseline
levels
alpha-fetoprotein,
treatment
history.
This
review
focuses
on
clinical
outcomes
these
key
trials,
retrospective
real-world
studies
discusses
future
perspectives
aim
to
provide
up-to-date
evidence
decision-making
aHCC.
Journal of Hepatocellular Carcinoma,
Journal Year:
2023,
Volume and Issue:
Volume 10, P. 1849 - 1859
Published: Oct. 1, 2023
To
compare
the
treatment
efficacy
and
safety
of
transarterial
chemoembolization
(TACE)
or
hepatic
arterial
infusion
chemotherapy
(HAIC)
combined
with
tyrosine
kinase
inhibitors
(TKIs)
programmed
cell
death
protein-1
(PD-1)
for
patients
unresectable
hepatocellular
carcinoma
(HCC).81
HCC
were
retrospectively
analyzed,
including
30
51
treated
either
TKIs
PD-1
TACE
(TTP)
HAIC
(HTP),
respectively.
Tumor
response
survival
outcomes
compared.The
median
overall
(mOS)
was
21.0
months
in
TTP
group
15.0
HTP
(P
=
0.525;
HR
1.23;
95%
CI
0.66-2.29).
The
progression-free
(mPFS)
6.7
9.9
0.160;
0.70;
0.42-1.16).
After
Propensity
Score
Matching
(PSM),
mOS
18.0
0.644;
1.20;
0.56-2.58).
mPFS
6.4
0.028;
0.49;
0.26-0.93).
disease
control
rate
(90.2%
vs
76.7%,
P
0.116,
before
PSM;
91.7%
75.0%,
0.121,
after
PSM)
intrahepatic
(94.1%
80.0%,
0.070,
79.2%,
0.220,
higher
than
group.Though
more
advanced
tumors,
clinical
are
comparable
to
TACE-based
combination
therapy
HCC.
Nevertheless,
significantly
improved
PFS
benefits
large
tumor
burden
vascular
invasion.
Pakistan Journal of Medical Sciences,
Journal Year:
2023,
Volume and Issue:
39(6)
Published: Sept. 11, 2023
Objectives:
To
investigate
the
impact
of
combining
lenvatinib
with
transarterial
chemoembolization
(TACE)
for
unresectable
hepatocellular
carcinoma
(HCC).
Methods:
This
was
a
retrospective
observational
study
which
reviewed
medical
records
103
HCC
patients
from
January
2017
to
June
2020
in
The
First
Affiliated
Hospital
Soochow
University.
It
included
46
who
received
TACE
plus
and
57
alone.
levels
serum
indicators,
clinical
effect,
adverse
events,
overall
survival
(OS),
progression-free
(PFS)
were
compared
between
two
groups.
Results:
AFP
VEGF
TACE+lenvatinib
group
post-treatment
significantly
lower
than
(P<0.05).
efficacy
(69.57%)
higher
that
(40.35%)
There
significant
differences
hypertension,
diarrhea,
bleeding
(gingiva)
groups
no
one
or
year
PFS
rate
OS
(P>0.05),
while
years
(P<0.05).
Conclusions:
combined
have
high
effective
rate,
reduced
levels,
acceptable
incidence
events.
doi:
https://doi.org/10.12669/pjms.39.6.7944
How
cite
this:
Long
J,
Liu
L,
Yang
X,
Lu
Qin
L.
Impact
Lenvatinib
Transarterial
carcinoma.
Pak
J
Med
Sci.
2023;39(6):---------.
is
an
Open
Access
article
distributed
under
terms
Creative
Commons
Attribution
License
(http://creativecommons.org/licenses/by/3.0),
permits
unrestricted
use,
distribution,
reproduction
any
medium,
provided
original
work
properly
cited.
F1000Research,
Journal Year:
2024,
Volume and Issue:
13, P. 104 - 104
Published: Feb. 16, 2024
Advanced
hepatocellular
carcinoma
(HCC)
is
traditionally
associated
with
limited
treatment
options
and
a
poor
prognosis.
Sorafenib,
multiple
tyrosine
kinase
inhibitor,
was
introduced
in
2007
as
first-in-class
systemic
agent
for
advanced
HCC.
After
sorafenib,
range
of
targeted
therapies
immunotherapies
have
demonstrated
survival
benefits
the
past
5
years,
revolutionizing
landscape
More
recently,
evidence
novel
combinations
agents
distinct
mechanisms
has
emerged.
In
particular,
combination
trials
on
atezolizumab
plus
bevacizumab
durvalumab
tremelimumab
shown
encouraging
efficacy.
Hence,
international
societies
revamped
their
guidelines
to
incorporate
new
recommendations
these
agents.
Aside
from
HCC,
indications
therapy
are
expanding.
For
example,
therapeutics
locoregional
(trans-arterial
chemoembolization
or
stereotactic
body
radiation
therapy)
promising
early
results
downstaging
Recent
also
explored
role
neoadjuvant
borderline-resectable
HCC
adjuvant
reduce
recurrence
risk
after
curative
resection.
Despite
clinical
trials,
real-world
efficacy
specific
patient
subgroups
(such
patients
cirrhosis,
high
bleeding
risk,
renal
impairment,
cardiometabolic
diseases)
remains
uncertain.
The
effect
liver
disease
etiology
warrants
further
research.
With
an
increased
understanding
pathophysiological
pathways
accumulation
data,
personalized
decisions
will
be
possible,
field
continue
evolve.
American Journal of Cancer Research,
Journal Year:
2024,
Volume and Issue:
14(5), P. 2216 - 2227
Published: Jan. 1, 2024
This
preclinical
study
explored
the
synergistic
potential
of
sorafenib
and
NK
cell
chemoimmunotherapy
to
combat
hepatocellular
carcinoma
(HCC)
in
a
rat
model.
We
aimed
enhance
cytotoxicity
through
IL-12/18
cytokines
supplementation
elucidate
underlying
molecular
mechanisms
driving
this
collaborative
antitumor
action.
Twenty-four
Sprague-Dawley
rats
were
divided
into
distinct
treatment
groups,
receiving
via
gavage
cells
catheterization
proper
hepatic
artery.
Tumor
growth
response
monitored
weekly
MRI
scans,
including
T1w,
T2w,
DCE,
DWI
sequences.
Histological
examinations
assessed
tumor
viability,
apoptosis
fraction,
microvessel
density.
The
combined
therapy
demonstrated
significant
inhibition
growth,
angiogenesis,
induction
durable
immunity
compared
either
modality
alone.
DCE-MRI
revealed
alterations
microvasculature,
highlighting
effectiveness
combination.
Our
findings
highlight
promise
sorafenib-augmented
as
therapeutic
strategy
for
HCC
management.
targeted
delivery
supplemented
effectively
enhanced
within
microenvironment,
leading
improved
responses.
Further
investigation
clinical
trials
is
warranted
validate
these
human
patients
explore
translational
approach.
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
0(0), P. 0 - 0
Published: Aug. 19, 2024
The
most
frequent
primary
liver
cancer
is
called
hepatocellular
carcinoma
(HCC),
which
presents
serious
clinical
difficulties
because
of
its
aggressiveness
and
frequently
late-stage
diagnosis.
A
significant
health
burden
in
Egypt
associated
with
hepatitis
C
virus
(HCV)
infection,
highly
prevalent.
Liver
resection
transplantation
are
two
possibilities
for
curative
treatment;
each
has
advantages
disadvantages
own.
For
tiny
tumors,
local
ablative
therapies
including
cryoablation,
microwave
ablation,
radiofrequency
ablation
(RFA)
work
well.
Systemic
sorafenib,
lenvatinib,
immunotherapy
essential
advanced
stages
HCC,
while
locoregional
therapies,
such
as
transarterial
chemoembolization
(TACE)
radioembolization
(TARE),
target
intermediate-stage
HCC.
Novel
approaches,
like
gene
therapy
combination
medicines,
demonstrate
the
continuous
progress
HCC
treatment.
In
order
to
improve
patient
outcomes,
effective
requires
a
multidisciplinary
strategy
that
includes
supportive
palliative
care.
Improving
prognosis
early
discovery
using
diagnostic
imaging
biomarkers,
well
screening
programs.
maximize
management
care,
it
crucial
comprehend
intricate
interactions
between
staging
systems,
prognostic
variables,
therapeutic
modalities.
Life,
Journal Year:
2024,
Volume and Issue:
14(11), P. 1430 - 1430
Published: Nov. 6, 2024
Hepatocellular
carcinoma
(HCC)
represents
a
major
public
health
concern
and
ranks
among
the
leading
cancer-related
mortalities
globally.
Due
to
frequent
late-stage
diagnosis
of
HCC,
therapeutic
options
remain
limited.
Emerging
evidence
highlights
critical
role
non-coding
RNAs
(ncRNAs)
in
regulation
Aurora
kinase
A
(AURKA),
one
key
hub
genes
involved
several
cancer
pathways.
Indeed,
dysregulated
interaction
between
ncRNAs
AURKA
contributes
tumor
development,
progression,
resistance.
This
review
delves
into
interplay
their
hepatocarcinogenesis.
Recent
findings
underscore
involvement
axis
development
progression.
Furthermore,
this
also
discusses
clinical
significance
targeting
ncRNA-AURKA
axes,
offering
new
perspectives
that
could
lead
innovative
strategies
aimed
at
improving
outcomes
for
HCC
patients.