Assessing hemorrhagic risks in combination therapy: implications of angiogenesis inhibitors and immune checkpoint inhibitors
Yuhui Yang,
No information about this author
Pingping Long,
No information about this author
Ying Tuo
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 10, 2025
Objective
This
study
aims
to
evaluate
the
hemorrhage
risk
in
solid
tumor
patients
receiving
angiogenesis
inhibitors
(AGIs),
immune
checkpoint
(ICIs),
and
their
combination
using
FDA
Adverse
Event
Reporting
System
(FAERS)
database.
Methods
Data
from
Q1
2011
Q4
2023
were
extracted
FAERS
database
for
treated
with
AGIs,
ICIs,
or
combination.
A
disproportionality
analysis
was
conducted
by
calculating
reporting
odds
ratio
(ROR)
corresponding
95%
confidence
interval
(CI),
as
well
Proportional
Ratio
(PRR),
identify
potential
safety
signals.
To
assess
whether
is
higher
therapy
compared
monotherapy,
additive
multiplicative
models
employed
interactions
between
single-agent
treatments.
Results
The
of
AGIs
ICIs
significantly
increased
hemorrhagic
adverse
events,
particularly
pulmonary
hemorrhage.
Hemorrhagic
events
common
females
(50.97%)
older
(aged
64+),
frequently
occurring
within
first
30
days
treatment
(38.11%).
Gingival
(ROR
3,
PRR
418.9)
9.65,
1893.36)
most
AGI
group,
while
9.49,
1350.78)
2.6,
98.97)
prominent
ICI
group.
In
esophageal
variceal
40.72,
2344.72)
19.31,
1056.63)
exhibited
risks
Additive
indicated
that
excess
(RD
AB
=
0.01025,
P<0.001)
relative
(RR
1.99277,
than
those
suggesting
a
positive
interaction
drugs
further
increases
Conclusion
Our
demonstrates
raises
hemorrhage,
underscoring
urgent
need
enhanced
monitoring
protocols
clinical
practice
improve
efficacy
safety.
Language: Английский
Challenges and opportunities in single-domain antibody-based tumor immunotherapy
Xiaozhi Xi,
No information about this author
Guo Shu-hua,
No information about this author
Yuchao Gu
No information about this author
et al.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer,
Journal Year:
2025,
Volume and Issue:
unknown, P. 189284 - 189284
Published: Feb. 1, 2025
Language: Английский
Combination therapy with alisertib enhances the anti-tumor immunity induced by a liver cancer vaccine
Xue Fang,
No information about this author
Jing Yuan Liu,
No information about this author
Jinyan Wu
No information about this author
et al.
iScience,
Journal Year:
2025,
Volume and Issue:
28(4), P. 112120 - 112120
Published: March 15, 2025
Alisertib
is
a
potent
aurora
A
kinase
inhibitor
in
clinical
trials
for
cancer
treatment,
but
its
efficacy
on
vaccines
remains
unclear.
Here,
we
developed
DNA
vaccine
targeting
glypican-3
(pGPC3)
and
evaluated
with
alisertib
hepatocellular
carcinoma
(HCC)
models.
The
combination
therapy
of
pGPC3
significantly
inhibited
subcutaneous
tumor
growth,
enhanced
the
induction
maturation
CD11c+
CD8+CD11c+
dendritic
cells
(DCs),
expanded
tumor-specific
CD8+
T
cell
responses.
depletion
abolished
anti-tumor
effects,
underscoring
essential
role
functional
Moreover,
combined
treatment
promoted
memory
induction,
providing
long-term
protection.
In
liver
orthotopic
models,
demonstrated
therapeutic
through
These
results
indicate
that
enhances
vaccine's
effect,
offering
promising
strategy
HCC
treatment.
Language: Английский
RNF2 induces myeloid-derived suppressor cells chemotaxis and promotes hepatocellular carcinoma progression through the TRAF2-NF-κB signaling axis
Manman Liang,
No information about this author
Jianghua Yang,
No information about this author
Aiping Zhang
No information about this author
et al.
Cancer Immunology Immunotherapy,
Journal Year:
2025,
Volume and Issue:
74(5)
Published: March 27, 2025
Language: Английский
Next‐Generation Flexible Embolic Systems: Targeted Transarterial Chemoembolization Strategies for Hepatocellular Carcinoma
Han Wu,
No information about this author
Shao-Dong Lv,
No information about this author
Renjie Zhang
No information about this author
et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
Abstract
Transarterial
chemoembolization
(TACE)
remains
the
gold
standard
for
treating
intermediate‐stage
hepatocellular
carcinoma
(HCC),
yet
faces
great
challenges
in
overcoming
tumor
heterogeneity,
hypoxia‐induced
angiogenesis,
and
metastatic
progression.
The
development
of
advanced
flexible
embolization
materials
marks
a
revolutionary
leap
interventional
therapy,
offering
opportunities
to
revolutionize
precision,
drug
delivery
kinetics,
microenvironment
modulation.
This
comprehensive
review
systematically
examines
paradigm
shift
toward
next‐generation
TACE
technology,
emphasizing
limitations
conventional
approaches
innovations
embolic
agents.
A
detailed
discussion
nano‐flexible
systems
is
presented,
their
unique
coagulation
dynamics,
real‐time
imaging
capabilities,
therapeutic
precision.
delves
into
groundbreaking
strategies
integrating
hypoxia
modulation,
energy
conversion
therapeutics,
sophisticated
engineering.
Clinical
translation
aspects
are
thoroughly
explored,
including
large‐scale
trial
outcomes,
vascular
recanalization
patient‐specific
treatment
optimization.
Looking
forward,
key
frontiers
field
identified:
intelligent
nanocomposite
systems,
synergistic
combination
therapies,
precision
medicine
tailored
individual
biology.
work
not
only
objectively
evaluates
current
progress
but
also
charts
future
research
priorities,
aiming
transform
from
palliative
intervention
platform
ultimately
reshaping
landscape
HCC
patient
care.
Language: Английский
Comparative efficacy of interventional therapy with or without targeted immunotherapy in Child-Pugh B hepatocellular carcinoma patients: a single-center, retrospective study
Xufeng Guo,
No information about this author
Man Zhao,
No information about this author
Xiaoling Duan
No information about this author
et al.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
15
Published: May 1, 2025
Background
Current
large
clinical
trials
mainly
focus
on
Child-Pugh
A
(CP-A)
stage
hepatocellular
carcinoma
(HCC)
patients,
with
limited
data
CP-B
patients
especially
those
classified
as
B8-9,
whose
treatment
needs
remain
inadequately
addressed.
This
study
aims
to
evaluate
the
safety
efficacy
of
interventional
treatments,
or
without
targeted-immunotherapy
and
characteristics
HCC
receiving.
Methods
single-center
retrospective
investigation
incorporated
119
were
stratified
into
two
cohorts:
therapy
cohort
(42)
combined
targeted
immunotherapy
(77).
The
data,
overall
survival
(OS),
progression-free
(PFS),
therapeutic
both
groups
meticulously
recorded
comprehensively
analyzed.
Survival
disparities
statistically
compared
employing
Kaplan-Meier
analysis
method
log-rank
test.
Tumor
remission
was
appraised
in
accordance
RECIST
1.1
mRECIST
criteria.
Independent
influencing
factors
discerned
through
multifactorial
COX
regression
analysis.
Subsequently,
prediction
models
constructed
generate
column
line
graphs,
profiles
adverse
events
associated
diverse
modalities
also
evaluated.
Results
grade
included,
median
(mOS)
who
received
combination
21.4
months
(vs
13.2,
P=0.038)
superior
that
therapy,
(mPFS)
12.7
10.9
months,
P=0.183)
not
significantly
improved.
OS
group
B7
24.6
11.9,
P=0.006)
intervention,
while
there
no
significant
improvement
B8-9.
objective
rate
(ORR)
higher
than
intervention
(RECIST:
32.5%
vs
11.9%,
P
=
0.014;
mRECIST:
48.1%
23.8%,
0.010).
Except
for
score
progression
(P
0.003),
difference
occurrence
all-grade
≥grade
3
>
0.05).
Conclusion
Interventional
can
be
a
safe
effective
B
setting
controlled
liver
function
impairment.
Language: Английский
Anti-Cancer Drugs: Trends and Insights from PubMed Records
Pharmaceutics,
Journal Year:
2025,
Volume and Issue:
17(5), P. 610 - 610
Published: May 4, 2025
Background:
In
recent
years,
there
has
been
an
exponential
growth
in
global
anti-cancer
drug
research,
prompting
the
necessity
for
comprehensive
analyses
of
publication
output
and
thematic
shifts.
Methods:
This
study
utilized
a
set
PubMed
records
from
1962
to
2024
examined
patterns,
content
classification,
co-occurrence
key
pharmacological
molecular
terms.
Results:
Our
results
highlight
rise
publications,
with
annual
compound
rate
over
14%,
influenced
by
advancements
digital
knowledge
sharing
novel
therapeutic
breakthroughs.
A
pronounced
surge
occurred
during
COVID-19
pandemic,
suggesting
sustained
shift
research
dynamics.
The
revealed
strong
emphasis
on
classical
chemotherapeutic
agents—often
studied
combination
targeted
therapies
or
immunotherapies—and
growing
focus
immune
checkpoint
inhibitors
vaccine
platforms.
Furthermore,
networks
indicated
robust
links
between
chemotherapy
supportive
care,
as
well
emerging
synergies
immuno-oncology,
precision
medicine
approaches.
Conclusions:
suggests
that
while
modalities
are
reshaping
treatment
paradigms,
remains
central,
underscoring
value
integrative
regimens.
trend
toward
personalized,
combination-based
strategies
indicates
transformative
era
oncology
where
multidimensional
data
assessment
is
instrumental
guiding
future
innovations.
Language: Английский
Immune Microenvironment and the Effect of Vascular Endothelial Growth Factor Inhibition in Hepatocellular Carcinoma
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(24), P. 13590 - 13590
Published: Dec. 19, 2024
Systemic
therapy
for
unresectable
hepatocellular
carcinoma
(HCC)
has
progressed
with
the
development
of
multiple
kinases,
such
as
vascular
endothelial
growth
factor
(VEGF)
signaling,
targeting
cancer
and
angiogenesis.
Additionally,
efficacy
sorafenib,
regorafenib,
lenvatinib,
ramucirumab,
cabozantinib
been
demonstrated
in
various
clinical
trials,
they
are
now
widely
used
practice.
Furthermore,
effective
immune
checkpoint
inhibitors
systemic
HCC,
atezolizumab
+
bevacizumab
(atezo/bev)
durvalumab
tremelimumab
recommended
first-line
treatment.
Atezo/bev
therapy,
which
combines
an
anti-programmed
cell
death
1
ligand
antibody
anti-VEGF
antibody,
is
first
immunotherapy
to
demonstrate
against
HCC.
With
increasing
popularity
these
treatments,
VEGF
inhibition
attracting
attention
from
perspective
its
anti-angiogenic
effects
impact
on
cancer-immune
cycle.
In
this
review,
we
outline
role
tumor
microenvironment
cycle
HCC
potential
regulatory
mechanisms
VEGF.
consider
significance
dual
angiogenesis
immune-related
molecules
by
VEGF,
ultimately
aim
clarify
latest
treatment
strategies
that
maximizes
efficacy.
Language: Английский
Advances on the role of stem cells in liver cancer
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 12
Published: Dec. 31, 2024
Liver
cancer,
especially
hepatocellular
carcinoma
(HCC),
is
one
of
the
most
common
malignant
tumors
worldwide,
and
its
high
mortality
rate
treatment
difficulty
have
always
been
major
challenges
faced
by
medical
community.
With
continuous
development
biotechnology,
stem
cell
research
has
shown
great
potential
hope
in
liver
cancer
treatment.
This
review
provides
a
brief
overview
importance
cells
research,
including
identification
(LCSCs),
molecular
maintenance
mechanisms
stemness
LCSCs,
targeted
therapy
strategies,
as
well
therapy,
proposing
future
directions.
Language: Английский