Biomarker Research,
Journal Year:
2024,
Volume and Issue:
12(1)
Published: Oct. 18, 2024
Treatment
based
on
immune
checkpoint
blockade
has
revolutionized
cancer
therapy.
Despite
the
remarkable
success
achieved
and
preclinical
development
of
multiple
inhibitors
targeting
other
checkpoints,
only
antibodies
PD-1/PD-L1
axis
CTLA-4
have
been
approved
for
patient
treatment,
especially
in
solid
tumors.
Currently,
with
approval
relatlimab,
a
LAG-3
blocking
antibody,
third
player,
used
fight
against
cancer.
The
endorsement
relatlimab
marks
significant
milestone
immunotherapy,
opening
new
avenues
combination
therapies
enhancing
treatment
outcomes.
However,
complex
biology
may
hinder
its
full
as
therapeutic
alternative.
In
this
review,
we
provide
in-depth
insight
into
current
future
treatment.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 15, 2025
Abstract
The
concomitant
development
and
evolution
of
lung
computed
tomography
(CT)
artificial
intelligence
(AI)
has
allowed
non-invasive
imaging
to
be
a
key
part
the
clinical
care
patients
with
major
diseases,
such
as
cancer.
However,
paucity
labeled
CT
data
limited
training
highly
efficacious
AI
models
thereby
retarded
broad-scale
adoption
deployment
AI-based
in
real-world
setting.
In
this
paper,
We
introduce
LCTfound,
foundational
model
that
encodes
images
along
correlated
information,
into
neural
network.
LCTfound
used
self-supervised
learning
pre-trained
by
diffusion
using
large
dataset
containing
105,184
scans
(totaling
more
than
28
million
images)
from
multiple
centers.
was
evaluated
on
8
categories
tasks,
ranging
scanning-level
diagnosis
pixel-level
image
restoration,
including
segmentation
mediastinal
neoplasm,
pulmonary
alveolar
proteinosis,
prognosis
non-small
cell
cancer,
prediction
pathological
response
neoadjuvant
chemoimmunotherapy,
whole
3D
modeling
for
surgical
navigation,
virtual
angiography(CTA),
reconstruction
sparse
views,
enhancement
low-dose
images.
Equipped
robust
few-shot
capability,
outperformed
previously
state-of-the-art
all
above
tasks.
is
advancements
representation
CT,
laying
groundwork
operates
high
efficacy
across
spectrum
low-level
high-level
tasks
serving
dual
purpose
aiding
diseases
improving
quality
imaging.
Lung Cancer,
Journal Year:
2025,
Volume and Issue:
200, P. 108076 - 108076
Published: Jan. 2, 2025
The
peri-operative
management
of
non-small
cell
lung
cancer
(NSCLC)
in
earlier
stage
disease
has
seen
significant
advances
recent
years
with
the
incorporation
immune
checkpoint
inhibitors
and
targeted
therapy.
However,
many
unanswered
questions
challenges
remain,
including
application
clinical
trial
data
to
routine
practice.
Recognising
unique
demographic
profile
Asian
patients
NSCLC
heterogeneous
healthcare
systems,
Thoracic
Oncology
Research
Group
(ATORG)
convened
a
consensus
meeting
Singapore
on
26
April
2024
discuss
relevant
issues
spanning
diagnostic
testing
post-neoadjuvant
treatment
considerations
future
directions.
An
interdisciplinary
group
19
experts
comprising
medical
oncologists,
thoracic
surgeons,
radiation
pulmonologists
pathologists
from
Singapore,
Hong
Kong,
Mainland
China,
Korea,
Japan,
Taiwan,
India,
Malaysia,
Thailand,
Vietnam
Australia
met
emerging
data,
identify
existing
gaps
care
develop
multidisciplinary,
multinational
expert
statement
tailored
Asia-Pacific
region.
Current Oncology,
Journal Year:
2025,
Volume and Issue:
32(4), P. 239 - 239
Published: April 19, 2025
Worldwide,
about
two
million
people
are
diagnosed
with
lung
cancer
each
year,
85%
of
whom
have
non-small
cell
(NSCLC).
Recent
progress
in
treating
advanced/metastatic
NSCLC
targeted
therapies
has
shifted
attention
to
early
(Stages
I–IIIA)
and
perioperative
(neoadjuvant
adjuvant)
systemic
therapies.
However,
our
comprehension
how
therapeutics
incorporated
into
care
their
impact
on
patient
outcomes
is
just
starting
unfold.
Methods:
This
retrospective
observational
study
used
a
US
nationwide
electronic
health
record-derived
deidentified
database
spanning
January
2019–March
2024
aimed
describe
(1)
eNSCLC
demographic
clinical
characteristics,
(2)
real-world
neoadjuvant
adjuvant
use,
(3)
outcomes.
Results:
The
population
included
4841
Stage
IB–IIIA
patients
mean
age
70.9
±
8.6
years.
majority
(69.9%)
received
definitive
treatment:
surgery
(n
=
2280),
radiation
320),
or
chemoradiation
783),
while
30.1%
1458)
did
not.
Many
treatment
some
therapy
(surgery:
52.6%,
radiation:
52.2%,
chemoradiation:
75.5%).
Neoadjuvant
use
was
limited
all
groups
8.2%,
6.1%,
11.6%).
Among
the
54.6%
receiving
adjuvant,
immune
checkpoint
inhibitors
were
most
common
choice
for
(39.1%)
(73.7%)
patients,
surgical
predominantly
platinum-doublet
(37.0%).
Surgical
similar
across
groups,
without
had
lower
survival
rates.
Conclusions:
In
this
study,
we
found
that
although
underwent
form
treatment,
limited,
rarely
care.
A
crucial
initial
step
improving
understand
address
underutilization
neoadjuvant/adjuvant
patients.
Breathe,
Journal Year:
2024,
Volume and Issue:
20(2), P. 230219 - 230219
Published: June 1, 2024
Chest
radiography,
computed
tomography
(CT)
and
positron
emission
(PET)-CT
are
required
for
staging
nonsmall
cell
lung
cancers.
Stage
I
cancers
may
be
up
to
4
cm
in
maximal
diameter,
with
stage
IA
tumours
being
3
IB
cm.
A
cancer
becomes
II
if
the
tumour
is
between
≤5
(stage
IIA),
or
it
spreads
ipsilateral
peribronchial
hilar
lymph
nodes
IIB).
should
surgically
resected,
ideally
using
minimally
invasive
methods.
Lobectomy
usually
performed,
although
some
studies
have
shown
good
outcomes
sublobar
resections.
If
surgery
not
possible,
stereotactic
body
radiotherapy
a
alternative.
This
involves
delivering
few
high-dose
radiation
treatments
at
very
high
precision.
For
IIB
disease,
combinations
of
surgery,
chemotherapy
immunotherapy
used.
There
evidence
that
neoadjuvant
treatment
(immunotherapy
nivolumab
II)
optimises
outcomes.
Adjuvant
platinum-based
doublet
(typically
cisplatin+vinorelbine)
offered
resected
considered
IIA
tumours.
pembrolizumab
used
IB–IIIA
following
resection
adjuvant
chemotherapy.
Osimertinib
IIIA
which
relevant
mutations
(epidermal
growth
factor
receptor
exon
19
deletions
21
(L858R)
substitution).
no
fixed
guidelines
follow-up,
but
most
centres
recommend
6-monthly
CT
scanning
first
2–3
years
after
definitive
treatment,
followed
by
annual
scans.
Cancer Immunology Immunotherapy,
Journal Year:
2025,
Volume and Issue:
74(2)
Published: Jan. 3, 2025
Checkpoint
inhibitor
pneumonitis
(CIP)
that
develops
following
immune
checkpoint
(ICI)
treatment
can
be
difficult
to
distinguish
from
other
common
etiologies
of
lung
inflammation
in
cancer
patients.
Here,
we
evaluate
the
bronchoalveolar
lavage
fluid
(BAL)
for
potential
biomarkers
specific
CIP.
We
conducted
a
retrospective
study
patients
who
underwent
standard
care
bronchoscopy
compare
cytokines
interest
between
with
and
without
CIP
immune-mediated
pulmonary
diseases.
Pulmonary
diagnoses
were
determined
by
treating
clinician
at
time
retroactively
reviewed
agreement
team.
Thirty-seven
included,
24
(64.9%)
had
infection,
2
(5.4%)
edema,
6
(16.2%)
non-CIP
drug-induced
pneumonitis,
3
(8.1%)
CIP,
5
(13.5%)
ILD
or
autoimmune
vasculitis,
4
(10.8%)
progression,
nonimmune-mediated
interstitial
disease
(ILD).
IL-6
BAL
was
significantly
higher
compared
those
progression
ILD,
diseases
infection.
distinguished
common,
important
causes
infiltrates
cancer,
suggesting
it
may
give
insight
into
pathophysiology
has
as
biomarker.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Jan. 27, 2025
Background
There
is
no
neoadjuvant
immunotherapy
for
early-stage
oral
cancer
patients.
We
report
a
single-arm,
open-label,
pilot
clinical
trial
assessing
the
efficacy
and
safety
of
topical
toll-like
receptor-7
(TLR-7)
agonist,
imiquimod,
utilized
in
setting
squamous
cell
carcinoma
(OSCC).
Methods
The
primary
endpoint
reduction
tumor
counts
assessed
by
quantitative
multiplex
immunofluorescence
immune-related
pathologic
response.
secondary
safety.
Results
60%
patients
experienced
50%
or
greater
count
post-treatment
(95%
CI
=
32%
to
84%).
Similarly,
had
major
response
(irMPR)
with
two
complete
responses,
40%
partial
(PR)
percent
residual
viable
ranging
from
25%
65%.
An
increase
functional
helper
cytotoxic
T-cells
significantly
contributed
(R=0.54
0.55,
respectively).
treatment
was
well
tolerated
application
site
mucositis
being
most
common
adverse
event
(grades
1-3),
grade
4
life-threatening
event.
median
follow-up
time
17
months
16
-
not
reached),
one-year
recurrence-free
survival
93%
evaluable
Conclusion
Neoadjuvant
imiquimod
could
be
safe
promising
regimen
cancer.
Trial
registration
ClinicalTrials.gov,
Identifier
NCT04883645.
General Thoracic and Cardiovascular Surgery Cases,
Journal Year:
2025,
Volume and Issue:
4(1)
Published: Feb. 3, 2025
Abstract
Background
Preoperative
nivolumab
combination
chemotherapy
has
shown
its
efficacy
in
resectable
stage
II–III
non-small
cell
lung
cancer
and
become
one
of
the
standard
treatments.
While
preoperative
is
generally
a
regimen
three
cycles,
when
treatment
prematurely
discontinued
remains
unclear.
Case
presentation
An
81-year-old
man
was
diagnosed
as
adenocarcinoma
(cT3N1M0,
cStage
IIIA).
A
computed
tomography
(CT)
showed
58
mm
mass
left
upper
lobe
with
an
intrapulmonary
metastasis,
positron-emission
tomography/CT
suggested
metastatic
lymph
nodes
at
pulmonary
hilum.
+
carboplatin
paclitaxel
were
administered;
however,
after
first
cycle,
due
to
grade
3
anorexia,
1
body
weight
loss,
4
neutropenia.
It
affair
that
continuation
therapy
made
him
unsuitable
for
surgery,
CT
scan
reduction
tumor
size
20
mm.
Then,
we
decided
discontinue
perform
surgery.
Video-assisted
thoracoscopic
lobectomy
node
dissection
performed,
postoperative
course
uneventful.
The
pathological
examination
revealed
15%
residual
primary
lesion
no
diagnosed.
patient
did
not
undergo
adjuvant
chemotherapy,
recurrence
observed
1.5
years
surgery
Conclusions
In
this
case,
combined
only
cycle
adverse
events;
significant
effect
achieved.
Therefore,
even
it
unable
continue
therapy,
important
miss
chance
good
may
have
been
Cancers,
Journal Year:
2025,
Volume and Issue:
17(4), P. 668 - 668
Published: Feb. 16, 2025
The
treatment
of
epidermal
growth
factor
receptor
(EGFR)-mutant
non-small-cell
lung
cancer
(NSCLC)
patients
was
dramatically
revolutionized
by
the
introduction
EGFR
tyrosine
kinase
inhibitors
in
clinical
practice,
both
advanced
and
locally
advanced/early
stages.
present
work
focuses
on
osimertinib
use
early
NSCLC
Phase
3
trials
have
supported
as
new
standard
care,
adjuvant
setting
disease.
ADAURA
study
reported
an
overall
survival
(OS)
advantage
for
completely
resected
stage
II-IIIA
EGFR-mutant
tumors,
while
LAURA
proved
a
statistically
significant
benefit
progression-free
(PFS)
delay
central
nervous
system
metastasis
development
treated
with
maintenance
after
concurrent
chemoradiotherapy
In
neoadjuvant
setting,
data
osimertinib’s
efficacy
are
conflicting;
therefore,
Neo-ADAURA
is
evaluating
safety
alone
or
combination
chemotherapy
II-IIIB
common
mutations.
We
discuss
several
issues
that
need
to
be
clarified,
such
drug
uncommon
mutations,
long-term
impact
survival,
management
resistance
mechanisms.
Moreover,
we
report
studies
trying
identify
potential
biomarkers
response,
circulating
tumor
DNA
(ctDNA),
aim
selecting
who
will
most
from
osimertinib.