Cureus,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 17, 2024
Theranostics,
a
remarkable
combination
of
diagnostics
and
therapeutics,
has
given
rise
to
tissue/organ-format
theranostic
scaffolds
that
integrate
targeted
therapy
real-time
disease
monitoring.
The
scaffold
is
3D
structuring
template
for
cell
or
tissue
attachment
growth.
These
offer
unprecedented
opportunities
personalized
medicine
hold
great
potential
revolutionizing
healthcare.
Recent
advancements
in
fabrication
techniques
have
enabled
the
creation
highly
intricate
precisely
engineered
with
controllable
physical
chemical
properties,
enhancing
their
therapeutic
engineering
regenerative
medicine.
This
paper
proposes
new
categorization
method
based
on
relativity
design-independent
parameters.
Five
types
are
defined
at
different
levels,
highlighting
importance
understanding
analyzing
types.
It
possesses
ability
seamlessly
therapeutics
within
single
platform,
efficacy
precision
Natural
derived
from
biomaterials
synthetic
fabricated
by
human
intervention
discussed,
offering
advantages
such
as
tunable
mechanical
properties
controlled
drug
delivery,
while
natural
provide
inherent
biocompatibility
bioactivity,
making
them
ideal
promoting
cellular
responses.
use
shows
promise
advancing
improving
patient
outcomes.
transfer
technologies
changes
society
accelerated
evolution
health
monitoring
into
era
personal
Using
emerging
data,
cost-effective
analytics,
wireless
sensor
networks,
mobile
smartphones,
easy
internet
access,
these
expected
accelerate
transition
outside
traditional
healthcare
settings.
main
objective
this
review
article
comprehensive
overview
applications
current
biomedical
research,
dual
role
diagnostics.
aims
explore
latest
design,
fabrication,
functionalization,
emphasizing
how
innovations
contribute
improved
efficacy,
progression
across
various
medical
fields.
ESMO Open,
Journal Year:
2022,
Volume and Issue:
7(2), P. 100399 - 100399
Published: Feb. 21, 2022
Liquid
biopsy
(LB)
is
a
rapidly
evolving
diagnostic
tool
for
precision
oncology
that
has
recently
found
its
way
into
routine
practice
as
an
adjunct
to
tissue
(TB).
The
concept
of
LB
refers
any
tumor-derived
material,
such
circulating
tumor
DNA
(ctDNA)
or
cells
are
detectable
in
blood.
An
not
limited
the
blood
and
may
include
other
fluids
cerebrospinal
fluid,
pleural
effusion,
urine,
among
others.
Nature Medicine,
Journal Year:
2024,
Volume and Issue:
30(3), P. 716 - 729
Published: Feb. 13, 2024
Abstract
For
patients
with
non-small-cell
lung
cancer
(NSCLC)
tumors
without
currently
targetable
molecular
alterations,
standard-of-care
treatment
is
immunotherapy
anti-PD-(L)1
checkpoint
inhibitors,
alone
or
platinum-doublet
therapy.
However,
not
all
derive
durable
benefit
and
resistance
to
immune
blockade
common.
Understanding
mechanisms
of
resistance—which
can
include
defects
in
DNA
damage
response
repair
pathways,
alterations
functional
mutations
STK11
/LKB1,
antigen-presentation
immunosuppressive
cellular
subsets
within
the
tumor
microenvironment—and
developing
effective
therapies
overcome
them,
remains
an
unmet
need.
Here
phase
2
umbrella
HUDSON
study
evaluated
rational
combination
regimens
for
advanced
NSCLC
following
failure
anti-PD-(L)1-containing
A
total
268
received
durvalumab
(anti-PD-L1
monoclonal
antibody)–ceralasertib
(ATR
kinase
inhibitor),
durvalumab–olaparib
(PARP
durvalumab–danvatirsen
(STAT3
antisense
oligonucleotide)
durvalumab–oleclumab
(anti-CD73
antibody).
Greatest
clinical
was
observed
durvalumab–ceralasertib;
objective
rate
(primary
outcome)
13.9%
(11/79)
versus
2.6%
(5/189)
other
regimens,
pooled,
median
progression-free
survival
(secondary
5.8
(80%
confidence
interval
4.6–7.4)
2.7
(1.8–2.8)
months,
overall
17.4
(14.1–20.3)
9.4
(7.5–10.6)
months.
Benefit
durvalumab–ceralasertib
consistent
across
known
immunotherapy-refractory
subgroups.
In
ATM
-altered
hypothesized
harbor
vulnerability
ATR
inhibition,
26.1%
(6/23)
survival/median
were
8.4/22.8
Durvalumab–ceralasertib
safety/tolerability
profile
manageable.
Biomarker
analyses
suggested
that
anti-PD-L1/ATR
inhibition
induced
changes
reinvigorated
antitumor
immunity.
under
further
investigation
NSCLC.
ClinicalTrials.gov
identifier:
NCT03334617
The Lancet Regional Health - Europe,
Journal Year:
2024,
Volume and Issue:
38, P. 100838 - 100838
Published: March 1, 2024
In
the
past
two
decades,
treatment
of
metastatic
non-small
cell
lung
cancer
(NSCLC),
has
undergone
significant
changes
due
to
introduction
targeted
therapies
and
immunotherapy.
These
advancements
have
led
need
for
predictive
molecular
tests
identify
patients
eligible
therapy.
This
review
provides
an
overview
development
current
application
biomarker
testing
in
European
with
advanced
stage
NSCLC.
Using
data
from
eleven
countries,
we
conclude
that
recommendations
are
incorporated
national
guidelines
across
Europe,
although
there
differences
their
comprehensiveness.
Moreover,
availability
recently
EMA-approved
varies
between
countries.
Unfortunately,
routine
assessment
national/regional
rates
is
limited.
As
a
result,
it
remains
uncertain
which
proportion
NSCLC
Europe
receive
adequate
testing.
Lastly,
Molecular
Tumor
Boards
(MTBs)
discussion
test
results
widely
implemented,
but
composition
functioning
lacking.
The
establishment
MTB
can
provide
framework
interpreting
rare
or
complex
mutations,
facilitating
appropriate
decision-making,
ensuring
quality
control.
Clinical Cancer Research,
Journal Year:
2023,
Volume and Issue:
29(18), P. 3579 - 3591
Published: April 24, 2023
The
current
landscape
of
targeted
therapies
directed
against
oncogenic
driver
alterations
in
non-small
cell
lung
cancer
(NSCLC)
is
expanding.
Patients
with
EGFR-mutant
NSCLC
can
derive
significant
benefit
from
EGFR
tyrosine
kinase
inhibitor
(TKI)
therapy,
including
the
third-generation
TKI
osimertinib.
However,
invariably,
all
patients
will
experience
disease
progression
this
therapy
mainly
due
to
adaptation
cells
through
primary
or
secondary
molecular
mechanisms
resistance.
comprehension
and
access
tissue
cell-free
DNA
next-generation
sequencing
have
fueled
development
innovative
therapeutic
strategies
prevent
overcome
resistance
osimertinib
clinical
setting.
Herein,
we
review
biological
implications
ongoing
ESMO Open,
Journal Year:
2023,
Volume and Issue:
8(4), P. 101587 - 101587
Published: June 25, 2023
Biomarker
tests
in
lung
cancer
have
been
traditionally
ordered
by
the
treating
oncologist
upon
confirmation
of
an
appropriate
pathological
diagnosis.
The
delay
this
introduces
prolongs
yet
further
what
is
already
a
complex,
multi-stage,
pre-treatment
pathway
and
delays
start
first-line
systemic
treatment,
which
crucially
informed
results
such
analysis.
Reflex
testing,
responsibility
for
testing
agreed
range
biomarkers
lies
with
pathologist,
has
shown
to
standardise
expedite
process.
Twelve
experts
discussed
rationale
considerations
implementing
reflex
as
standard
clinical
practice.
The Oncologist,
Journal Year:
2023,
Volume and Issue:
28(5), P. 402 - 413
Published: Feb. 23, 2023
Abstract
The
objective
of
this
narrative
review
is
to
summarize
the
efficacy
and
safety
available
therapies
for
rearranged
during
transfection
(RET)
fusion-positive
non-small
cell
lung
cancer
(NSCLC),
including
in
patients
with
central
nervous
system
(CNS)
metastases.
Background
information
provided
on
RET
rearrangements
NSCLC
molecular
testing
options
as
well
an
overview
clinical
guidelines
testing,
which
recommend
broad
rearrangements.
potential
treatments
NSCLC,
multikinase
inhibitors,
RET-selective
pemetrexed-based
therapy,
immunotherapies
are
reviewed
from
Phase
I/II
`real-world’
studies,
alongside
primary
secondary
resistance
mechanisms.
selpercatinib
pralsetinib,
preferred
first-line
therapy
metastatic
recommended
subsequent
if
inhibitors
have
not
been
used
setting.
Therapeutic Advances in Medical Oncology,
Journal Year:
2024,
Volume and Issue:
16
Published: Jan. 1, 2024
Lung
cancer
poses
a
global
health
challenge
and
stands
as
the
leading
cause
of
cancer-related
deaths
worldwide.
However,
its
incidence,
mortality,
characteristics
are
not
uniform
across
all
regions
Understanding
factors
contributing
to
this
diversity
is
crucial
in
prevalent
disease
where
most
cases
diagnosed
advanced
stages.
Hence,
prevention
early
diagnosis
emerge
efficient
strategies
enhance
outcomes.
In
Western
societies,
tobacco
consumption
constitutes
primary
risk
factor
for
lung
cancer,
accounting
up
90%
cases.
other
geographic
locations,
different
significant
play
fundamental
role
development,
such
individual
genetic
predisposition,
or
exposure
carcinogens
radon
gas,
environmental
pollution,
occupational
exposures,
specific
infectious
diseases.
Comprehensive
clinical
molecular
characterization
recent
decades
has
enabled
us
distinguish
subtypes
with
distinct
phenotypes,
genotypes,
immunogenicity,
treatment
responses,
survival
rates.
The
ultimate
goal
prevent
individualize
management
each
community
improve
patient