Impact of Helicobacter pylori infection status on outcomes among patients with gastric cancer treated with immune checkpoint inhibitors: a systematic review and meta-analysis
Microbial Pathogenesis,
Journal Year:
2025,
Volume and Issue:
unknown, P. 107407 - 107407
Published: Feb. 1, 2025
Language: Английский
Updates from a single-center phase 2 study of PD-1 inhibitor combined with hypomethylating agent plus CAG regimen in patients with relapsed/refractory acute myeloid leukemia
Hui-Sheng Zhou,
No information about this author
Yong-Feng Su,
No information about this author
Jun Wang
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 17, 2025
Anti-PD-1
monotherapy
has
shown
limited
clinical
efficacy
in
patients
with
relapsed/refractory
acute
myeloid
leukemia
(r/r
AML).
Our
study
aimed
to
analyze
the
effectiveness
and
safety
of
combining
tislelizumab
a
hypomethylating
agent
(HMA)
plus
CAG
regimen
treating
r/r
AML,
an
increased
sample
size
comparison,
historical
control
group
for
more
reliable
data
support
(ClinicalTrials.gov
identifier
NCT04541277).
The
included
total
37
AML
who
received
+
HMA
regimen.
overall
response
rate
was
69.4%,
median
survival
12.1
months
event-free
6.2
months.
Multivariate
analysis
revealed
that
aged
40
or
above
exhibited
higher
rate,
while
those
lower
burden
(bone
marrow
blast
percentage
<40%)
demonstrated
improved
survival.
Additionally,
bridging
allogeneic
hematopoietic
stem
cell
transplantation
associated
extended
Grade
2-3
immune-related
adverse
events
were
observed
8.5%
patients,
no
deaths
directly
attributed
these
events.
After
propensity
score
matching,
inclusion
appeared
positively
influence
compared
controls
treated
Overall,
combination
rates
maintaining
low
incidence
severity
patients.
https://clinicaltrials.gov/,
NCT04541277.
Language: Английский
Nanotechnology-Enhanced siRNA Delivery: Revolutionizing Cancer Therapy
ACS Applied Bio Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 12, 2025
RNA
interference
(RNAi)
has
emerged
as
a
transformative
approach
for
cancer
therapy,
enabling
precise
gene
silencing
through
small
interfering
(siRNA).
However,
the
clinical
application
of
siRNA-based
treatments
faces
challenges
such
rapid
degradation,
inefficient
cellular
uptake,
and
immune
system
clearance.
Nanotechnology-enhanced
siRNA
delivery
revolutionized
therapy
by
addressing
these
limitations,
improving
stability,
tumor-specific
targeting,
therapeutic
efficacy.
Recent
advancements
in
nanocarrier
engineering
have
introduced
innovative
strategies
to
enhance
safety
precision
therapies,
offering
new
opportunities
personalized
medicine.
This
review
highlights
three
key
innovations
nanotechnology-enhanced
delivery:
artificial
intelligence
(AI)-driven
design,
multifunctional
nanoparticles
combined
strategies,
biomimetic
nanocarriers
enhanced
biocompatibility.
AI-driven
utilize
machine
learning
algorithms
optimize
nanoparticle
properties,
drug
release
profiles
minimizing
off-target
effects.
Multifunctional
integrate
with
chemotherapy,
immunotherapy,
or
photothermal
synergistic
treatment
approaches
that
outcomes
reduce
resistance.
Biomimetic
nanocarriers,
including
exosome-mimicking
systems
cell-membrane-coated
nanoparticles,
improve
circulation
time,
evasion,
targeted
tumor
delivery.
These
collectively
precision,
efficiency,
therapies.
The
scope
novelty
lie
their
ability
overcome
primary
barriers
while
paving
way
clinically
viable
solutions.
provides
comprehensive
analysis
latest
developments
fabrication,
preclinical
studies,
assessments.
By
integrating
multifunctionality,
biomimicry,
holds
immense
potential
future
therapy.
Language: Английский
Immunopharmacology of gastric cancer–deciphering immune cell subset responses and nanoparticle-mediated targeting
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: May 19, 2025
The
diverse
landscape
of
immune
cell
populations
significantly
influences
therapeutic
outcomes
in
advanced
gastric
cancer,
a
leading
cause
cancer
mortality
worldwide.
Progress
immunopharmacology,
aided
by
single-cell
analytics,
increasingly
highlights
complexity
and
functional
heterogeneity.
Conventional
categories
contain
subsets,
including
various
T
cells
(helper,
regulatory,
memory)
B
(plasma,
memory,
regulatory).
Innate
like
macrophages,
natural
killer
cells,
dendritic
also
exist
states.
These
subsets
exhibit
distinct
pharmacological
response
profiles
that
are
often
obscured
bulk
analyses.
This
review
explores
the
differential
responses
critical
within
tumor
microenvironment
to
current
modalities,
encompassing
cytotoxic
chemotherapy,
molecular
targeted
agents,
immunotherapies
such
as
checkpoint
inhibitors.
We
delve
into
processes
underlying
subset-specific
drug
effects,
potential
mechanisms
resistance
linked
specific
states,
influence
on
subset
pharmacology.
Furthermore,
we
discuss
application
nanoparticle-based
delivery
systems
specifically
engineered
target
subpopulations,
aiming
enhance
immunomodulatory
efficacy,
reshape
repertoires
favorably,
overcome
resistance,
minimize
toxicity
for
more
precise
effective
treatment
cancer.
Language: Английский
Tumor-Associated Macrophages: Polarization, Immunoregulation, and Immunotherapy
Cells,
Journal Year:
2025,
Volume and Issue:
14(10), P. 741 - 741
Published: May 19, 2025
Tumor-associated
macrophages’
(TAMs)
origin,
polarization,
and
dynamic
interaction
in
the
tumor
microenvironment
(TME)
influence
cancer
development.
They
are
essential
for
homeostasis,
monitoring,
immune
protection.
Cells
from
bone
marrow
or
embryonic
progenitors
dynamically
polarize
into
pro-
anti-tumor
M2
M1
phenotypes
based
on
cytokines
metabolic
signals.
Recent
advances
TAM
heterogeneity,
characterization,
immunological
responses,
therapy
described
here.
The
manuscript
details
functions
their
role
resistance
to
PD-1/PD-L1
blockade.
Similarly,
TAM-targeted
approaches,
such
as
CSF-1R
inhibition
PI3Kγ-driven
reprogramming,
discussed
address
immunity
suppression.
Furthermore,
innovative
biomarkers
combination
may
enhance
TAM-centric
therapies.
It
also
stresses
relevance
of
this
distinct
cell
human
health
disease,
which
could
impact
future
research
Language: Английский