International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(21), P. 11354 - 11354
Published: Oct. 22, 2024
Molecular
testing
is
recommended
in
patients
with
metastatic
non-small
cell
lung
cancer
(NSCLC),
but
the
extent
of
its
use
Poland
unknown.
The
aim
POL-MOL
study
was
to
investigate
frequency
using
molecular
Polish
NSCLC.
invited
oncologists
completed
two
questionnaires,
and
data
for
1001
undergoing
systemic
treatment
NSCLC
were
collected.
tests
following
genetic
mutations
recorded:
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: Nov. 28, 2023
The
advent
of
iPSCs
has
brought
about
a
significant
transformation
in
stem
cell
research,
opening
up
promising
avenues
for
advancing
cancer
treatment.
formation
is
multifaceted
process
influenced
by
genetic,
epigenetic,
and
environmental
factors.
offer
distinctive
platform
investigating
the
origin
cancer,
paving
way
novel
approaches
to
treatment,
drug
testing,
tailored
medical
interventions.
This
review
article
will
provide
an
overview
science
behind
iPSCs,
current
limitations
challenges
iPSC-based
therapy,
ethical
social
implications,
comparative
analysis
with
other
types
also
discuss
applications
tumorigenesis,
future
tumorigenesis
highlight
successful
case
studies
utilizing
research.
conclusion
summarize
advancements
made
research
importance
continued
investment
iPSC
unlock
full
potential
these
cells.
Advances in healthcare information systems and administration book series,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 19
Published: Feb. 14, 2024
The
integration
of
cutting-edge
technologies
into
health
literacy
and
medical
practice
presents
unprecedented
opportunities
ethical
challenges.
This
chapter
delves
the
technoethical
considerations
crucial
for
navigating
this
new
landscape,
guided
by
a
posthumanist
framework.
Embracing
framework
encourages
us
to
reevaluate
traditional
boundaries,
inviting
more
inclusive
understanding
humanity's
relationship
with
technology.
also
explores
intricate
between
technology
ethics,
advocating
that
ensures
technological
advancements
in
healthcare
are
employed
ethically,
responsibly,
deep
their
societal
impact.
By
doing
so,
serves
as
guiding
beacon
professionals,
technologists,
ethicists,
policymakers,
urging
future
where
human
values
coalesce
foster
ecosystem
is
not
only
advanced
but
compassionate,
equitable,
ethically
grounded.
Journal of Clinical Oncology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 6, 2025
PURPOSE
Datopotamab
deruxtecan
(Dato-DXd)
is
a
trophoblast
cell-surface
antigen-2–directed
antibody-drug
conjugate
with
highly
potent
topoisomerase
I
inhibitor
payload.
The
TROPION-Lung05
phase
II
trial
(ClinicalTrials.gov
identifier:
NCT04484142
)
evaluated
the
safety
and
clinical
activity
of
Dato-DXd
in
patients
advanced/metastatic
non–small
cell
lung
cancer
(NSCLC)
actionable
genomic
alterations
progressing
on
or
after
targeted
therapy
platinum-based
chemotherapy.
PATIENTS
AND
METHODS
Patients
received
6
mg/kg
once
every
3
weeks.
primary
end
point
was
objective
response
rate
(ORR)
by
blinded
independent
central
review.
Secondary
points
included
duration
(DOR),
safety,
tolerability,
survival.
RESULTS
Among
137
who
at
least
1
dose
Dato-DXd,
71.5%
three
lines
prior
therapies
for
disease.
Overall,
56.9%
had
EGFR
mutations
24.8%
ALK
rearrangements.
Median
treatment
4.4
months
(range,
0.7-20.6).
confirmed
ORR
35.8%
(95%
CI,
27.8
to
44.4)
overall,
43.6%
32.4
55.3)
23.5%
10.7
41.2)
those
rearrangements,
respectively.
median
DOR
7.0
4.2
9.8),
overall
disease
control
78.8%
71.0
85.3).
Grade
≥3
treatment-related
adverse
events
(TRAEs)
occurred
28.5%
patients.
most
common
TRAE
stomatitis
(preferred
term;
any
grade:
56.2%;
grade
≥3:
9.5%).
Five
(3.6%)
experienced
adjudicated
interstitial
disease/pneumonitis,
(0.7%)
5
event.
CONCLUSION
Encouraging
durable
antitumor
observed
this
heavily
pretreated
NSCLC
population
alterations.
toxicities
comparable
previous
observations,
no
new
signals
were
observed.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
14
Published: Jan. 4, 2024
Receptor
tyrosine
kinases
(RTKs)
play
a
crucial
role
in
cellular
signaling
and
oncogenic
progression.
Epidermal
growth
factor
receptor
kinase
inhibitors
(EGFR
TKIs)
have
become
the
standard
treatment
for
advanced
non-small
cell
lung
cancer
(NSCLC)
patients
with
EGFR-sensitizing
mutations,
but
resistance
frequently
emerges
between
10
to
14
months.
A
significant
this
is
of
human
EGFR
3
(HER3),
an
family
member.
Despite
its
significance,
effective
targeting
HER3
still
developing.
This
review
aims
bridge
gap
by
deeply
examining
HER3’s
pivotal
contribution
TKI
spotlighting
emerging
HER3-centered
therapeutic
avenues,
including
monoclonal
antibodies
(mAbs),
TKIs,
antibody-drug
conjugates
(ADCs).
Preliminary
results
indicate
combining
HER3-specific
treatments
TKIs
enhances
antitumor
effects,
leading
increased
objective
response
rate
(ORR)
prolonged
overall
survival
(OS)
resistant
cases.
Embracing
HER3-targeting
therapies
represents
transformative
approach
against
emphasizes
importance
further
research
optimize
patient
stratification
understand
mechanisms.
Cancers,
Journal Year:
2024,
Volume and Issue:
16(13), P. 2338 - 2338
Published: June 26, 2024
Non-small-cell
lung
cancer
(NSCLC)
comprises
approximately
85%
of
all
cases,
often
diagnosed
at
advanced
stages,
which
diminishes
the
effective
treatment
options
and
survival
rates.
This
systematic
review
assesses
utility
emerging
biomarkers-circulating
tumor
DNA
(ctDNA),
microRNAs
(miRNAs),
blood
mutational
burden
(bTMB)-enhanced
by
next-generation
sequencing
(NGS)
to
improve
diagnostic
accuracy,
prognostic
evaluation,
strategies
in
NSCLC.
Analyzing
data
from
37
studies
involving
10,332
patients
2020
2024,
highlights
how
biomarkers
like
ctDNA
PD-L1
expression
critically
inform
selection
personalized
therapies,
particularly
beneficial
stages
These
are
critical
for
assessments
dynamically
adapting
plans,
where
high
specific
genetic
mutations
(e.g.,
ALK
fusions,
EGFR
mutations)
significantly
guide
use
targeted
therapies
immunotherapies.
The
findings
recommend
integrating
these
into
standardized
clinical
pathways
maximize
their
potential
enhancing
precision,
ultimately
fostering
significant
advancements
oncology
improving
patient
outcomes
quality
life.
substantiates
predictive
value
emphasizes
need
ongoing
innovation
biomarker
research.
Cancer Cell International,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: March 2, 2024
Abstract
Background
Novel
therapeutic
targets
are
urgently
needed
for
treating
drug-resistant
non-small
cell
lung
cancer
(NSCLC)
and
overcoming
drug
resistance
to
molecular-targeted
therapies.
Regulator
of
G
protein
signaling
20
(RGS20)
is
identified
as
an
upregulated
factor
in
many
cancers,
yet
its
specific
role
the
mechanism
through
which
RGS20
functions
NSCLC
remain
unclear.
Our
study
aimed
identify
prognosis
delineate
associated
cellular
molecular
pathways.
Methods
Immunohistochemistry
tissue
microarray
were
used
verify
expression
between
patients.
CCK8
cloning
conducted
determine
proliferation
ability
H1299
Anip973
cells
vitro.
Furthermore,
Transcriptome
sequencing
was
performed
show
enrichment
genes
Immunofluorescence
detect
translocation
changes
YAP
nucleus.
Western
blotting
demonstrated
different
expressions
autophagy
Hippo-PKA
signal
pathway.
In
vitro
vivo
experiments
verified
whether
overexpression
affect
regulating
Hippo
Results
The
higher
found
be
significantly
correlated
with
a
poorer
five-year
survival
rate.
Further,
accelerated
by
increasing
autophagy.
Transcriptomic
suggested
involvement
pathway
action
NSCLC.
activation
reduced
phosphorylation
facilitated
nuclear
translocation.
Remarkably,
inhibiting
GA-017
promoted
activated
knock-down
cells.
However,
forskolin,
GPCR
activator,
increased
reversed
promoting
effect
RGS20-overexpressing
Lastly,
further
confirmed
aggravating
tumorigenicity,
proliferation.
Conclusion
findings
indicate
that
drives
triggering
via
inhibition
PKA-Hippo
signaling.
These
insights
support
promising
novel
marker
target
future
targeted
therapies
treatment.
Cancer Treatment Reviews,
Journal Year:
2024,
Volume and Issue:
124, P. 102691 - 102691
Published: Jan. 21, 2024
In
treating
diffuse
large
B-cell
lymphoma
(DLBCL),
oncologists
have
traditionally
relied
on
the
chemotherapy
backbone
of
R-CHOP
as
standard
care.
The
two
dangers
that
hematologist
must
navigate
between
are
aggressive
disease
(Charybdis
in
absence
therapy
destroys
systematically
all
ships)
and
toxicity
therapies
(Scylla
with
its
six
monstrous
heads
devour
crew
members
at
a
time),
hematologists
to
very
carefully
both.
Therefore,
three
different
strategies
were
employed
goal
improving
cure
rates:
de-escalating
regimens,
escalating
replacement
strategies.
With
strategy,
breakthrough
treatment
was
identified
polatuzumab
vedotin
(anti-CD79B
antibody/drug
conjugate)
plus
R-CHP.
However,
this
regimen
still
did
not
achieve
elusive
universal
rate.
Fortunately,
advances
genomic
molecular
technologies
allowed
for
an
improved
understanding
heterogenous
nature
help
develop
guide
more
targeted,
precise,
individualized
therapies.
Additionally,
new
pharmaceutical
led
development
novel
cellular
therapies,
such
CAR
T-cell
therapy,
could
be
effective,
while
maintaining
acceptable
safety
profile.
Thus,
we
aim
highlight
challenges
DLBCL
need
address
therapeutic
regimens
eventually
no
longer
tethered
backbone.
intersection
artificial
intelligence
multi-omics
(genomics,
epigenomics,
transcriptomics,
proteomics,
metabolomics),
propose
analyze
multidimensional
biologic
data
launch
decisive
attack
against
targeted
fashion.
JCO Oncology Practice,
Journal Year:
2024,
Volume and Issue:
20(3), P. 370 - 377
Published: Jan. 9, 2024
PURPOSE
Racial/ethnic
inequities
in
next-generation
sequencing
(NGS)
were
examined
for
patients
with
advanced
non–small-cell
lung
cancer
(aNSCLC)
at
the
practice
and
physician
levels
to
inform
policies
improve
equitable
quality
of
care.
METHODS
This
retrospective
study
used
a
nationwide
electronic
health
record–derived
deidentified
database
aNSCLC
diagnosed
between
April
2018
March
2022
community
setting.
Timely
NGS
was
an
result
initial
diagnosis
≤60
days
after
diagnosis.
We
studied
how
driven
by
(1)
non-Latinx
Black
(Black)
Latinx
patient
under-representation
high
testing
practices
versus
(2)
being
tested
lower
rates
than
White
(White)
patients,
even
same
practice.
defined
these
two
concepts
as
across
inequity
within
inequity,
respectively,
total
their
summation.
Mean
percentage
point
estimated
using
Bayesian
approach.
RESULTS
A
12,045
(9,981
White;
1,528
Black;
536
Latinx)
met
criteria.
At
level,
mean
difference
7.49
8.26
Latinx.
Within-
across-practice
contributed
(48%
v
52%)
(60%
40%).
7.73
8.81
patients.
across-physician
(77%
23%
67%
33%).
CONCLUSION
Within-practice,
across-practice,
main
contributors
testing,
requiring
suite
interventions
effectively
address
inequities.