Journal of Experimental & Clinical Cancer Research,
Год журнала:
2024,
Номер
43(1)
Опубликована: Сен. 2, 2024
Abstract
Pancreatic
ductal
adenocarcinoma
(PDAC)
is
frequently
detected
in
late
stages,
which
leads
to
limited
therapeutic
options
and
a
dismal
overall
survival
rate.
To
date,
no
robust
method
for
the
detection
of
early-stage
PDAC
that
can
be
used
targeted
screening
approaches
available.
Liquid
biopsy
allows
minimally
invasive
collection
body
fluids
(typically
peripheral
blood)
subsequent
analysis
circulating
tumor
cells
or
tumor-associated
molecules
such
as
nucleic
acids,
proteins,
metabolites
may
useful
early
diagnosis
PDAC.
Single
biomarkers
lack
sensitivity
and/or
specificity
reliably
detect
PDAC,
while
combinations
these
multimarker
panels
improve
blood
test-based
diagnosis.
In
this
narrative
review,
we
present
an
overview
different
liquid
discuss
validity
panels.
CA A Cancer Journal for Clinicians,
Год журнала:
2024,
Номер
74(4), С. 368 - 382
Опубликована: Март 22, 2024
Abstract
Multicancer
detection
(MCD)
tests
use
a
single,
easily
obtainable
biospecimen,
such
as
blood,
to
screen
for
more
than
one
cancer
concurrently.
MCD
can
potentially
be
used
improve
early
detection,
including
cancers
that
currently
lack
effective
screening
methods.
However,
these
have
unknown
and
unquantified
benefits
harms.
differ
from
conventional
in
the
organ
responsible
positive
test
is
unknown,
broad
diagnostic
workup
may
necessary
confirm
location
type
of
underlying
cancer.
Among
two
prospective
studies
involving
greater
16,000
individuals,
identified
those
who
had
some
without
recommended
tests,
pancreas,
ovary,
liver,
uterus,
small
intestine,
oropharyngeal,
bone,
thyroid,
hematologic
malignancies,
at
stages.
Reported
sensitivities
range
27%
95%
but
by
are
lower
stage
cancers,
which
treatment
toxicity
would
lowest
potential
cure
might
highest.
False
reassurance
negative
result
reduce
adherence,
risking
loss
proven
public
health
standard‐of‐care
screening.
Prospective
clinical
trials
needed
address
uncertainties
about
accuracy
detect
different
asymptomatic
whether
sufficiently
mortality
reduction,
degree
contribute
overdiagnosis
overtreatment,
work
equally
well
across
all
populations,
appropriate
evaluation
follow‐up
patients
with
test.
JAMA,
Год журнала:
2024,
Номер
331(22), С. 1910 - 1910
Опубликована: Апрель 7, 2024
Importance
Randomized
clinical
trials
of
cancer
screening
typically
use
cancer-specific
mortality
as
the
primary
end
point.
The
incidence
stage
III-IV
is
a
potential
alternative
point
that
may
accelerate
completion
randomized
screening.
Objective
To
compare
with
points
in
Design,
Setting,
and
Participants
This
meta-analysis
included
41
conducted
Europe,
North
America,
Asia
published
through
February
19,
2024.
Data
extracted
numbers
participants,
diagnoses,
deaths
intervention
comparison
groups.
For
each
trial,
effect
was
calculated
percentage
reduction
between
groups
participants
cancer.
Exposures
Randomization
to
test
or
group
trial
Main
Outcomes
Measures
End
were
compared
using
Pearson
correlation
coefficients
95%
CIs,
linear
regression,
fixed-effects
meta-analysis.
Results
tested
benefits
for
breast
(n
=
6),
colorectal
11),
lung
12),
ovarian
4),
prostate
other
cancers
4).
Correlation
reductions
varied
by
type
(
I
2
65%;
P
.02).
highest
screened
(Pearson
ρ
0.99
[95%
CI,
0.51-1.00])
0.92
0.72-0.98])
cancers,
moderate
0.70
−0.26
0.96]),
weak
0.39
−0.27
0.80])
−0.69
−0.99
0.81])
cancers.
Slopes
from
regression
estimated
1.15
cancer,
0.75
0.40
0.28
−3.58
suggesting
given
magnitude
produced
different
magnitudes
change
heterogeneity
.004).
Conclusions
Relevance
In
screening,
late-stage
be
suitable
some
types,
but
not
others.
These
results
have
implications
multicancer
tests.
Abstract
Circulating
free
tumor
DNA
(ctDNA)
analysis
is
gaining
popularity
in
precision
oncology,
particularly
metastatic
breast
cancer,
as
it
provides
non-invasive,
real-time
information
to
complement
tissue
biopsies,
allowing
for
tailored
treatment
strategies
and
improved
patient
selection
clinical
trials.
Its
use
early
cancer
has
been
limited
so
far,
due
the
relatively
low
sensitivity
of
available
techniques
a
setting
characterized
by
lower
levels
ctDNA
shedding.
However,
advances
sequencing
bioinformatics,
well
methylome
profiles,
have
led
an
increasing
interest
application
from
screening
curative
evaluation
minimal
residual
disease
(MRD)
detection.
With
multiple
prospective
trials
this
setting,
may
become
useful
practice.
This
article
reviews
data
regarding
analytical
validity
currently
tests
detection
potential
cancer.
Pharmacology & Therapeutics,
Год журнала:
2024,
Номер
256, С. 108613 - 108613
Опубликована: Фев. 16, 2024
Melanoma
is
the
most
aggressive
form
of
skin
cancer,
representing
approximately
4%
all
cutaneous
neoplasms
it
accounts
for
up
to
80%
deaths.
Advanced
stages
melanoma
involve
metastatic
processes
and
are
associated
with
high
mortality
morbidity,
mainly
due
rapid
dissemination
heterogeneous
responses
current
therapies
including
immunotherapy.
Indeed,
immune
checkpoints
inhibitors
(ICIs),
either
alone
or
in
combination
other
currently
used
(MM)
linked
an
increase
patient
survival.
Of
note,
number
therapeutic
regimens
MM
patients
using
ICIs
has
increased,
highlighting
a
growing
need
reliable
biomarkers
that
can
both
predict
monitor
response
ICIs.
In
this
context,
circulating
biomarkers,
such
as
DNA,
RNA,
proteins,
cells,
have
emerged
their
ability
detect
disease
status.
Moreover,
blood
tests
minimally
invasive
provide
attractive
option
avoiding
stressful
medical
procedures.
This
systematic
review
summarizes
evaluate
possibility
non-invasive
biomarker
signature
guide
decisions.
The
studies
reported
here
offer
valuable
insight
into
how
role
personalized
treatments
receiving
therapy,
emphasizing
rigorous
clinical
trials
confirm
findings
establish
standardized
Cancers,
Год журнала:
2024,
Номер
16(5), С. 862 - 862
Опубликована: Фев. 21, 2024
The
concept
and
policies
of
multicancer
early
detection
(MCED)
have
gained
significant
attention
from
governments
worldwide
in
recent
years.
In
the
era
burgeoning
artificial
intelligence
(AI)
technology,
integration
MCED
with
AI
has
become
a
prevailing
trend,
giving
rise
to
plethora
products.
However,
due
heterogeneity
both
targets
technologies,
overall
diversity
products
remains
considerable.
types
encompass
protein
biomarkers,
cell-free
DNA,
or
combinations
these
biomarkers.
development
models,
different
model
training
approaches
are
employed,
including
datasets
case-control
studies
real-world
cancer
screening
datasets.
Various
validation
techniques,
such
as
cross-validation,
location-wise
validation,
time-wise
used.
All
factors
show
impacts
on
predictive
efficacy
AIs.
After
completion
development,
deploying
AIs
clinical
practice
presents
numerous
challenges,
presenting
reports,
identifying
potential
locations
tumors,
addressing
cancer-related
information,
follow-up
treatment.
This
study
reviews
several
mature
currently
available
market,
detecting
their
composing
serum
biomarker
detection,
training/validation,
application.
review
illuminates
challenges
encountered
by
existing
across
stages,
offering
insights
into
continued
obstacles
within
field
AI.
Cancer Discovery,
Год журнала:
2024,
Номер
14(4), С. 600 - 604
Опубликована: Апрель 4, 2024
Summary:
Rapid
advances
in
technology
and
therapeutics,
along
with
better
methods
to
discern
who
is
at
risk
for
cancer
by
genetic
testing
other
means,
has
enabled
the
development
of
interception.
Targeted
therapies
“immuno-interception”
may
eliminate
premalignant
lesions
require
clinical
trial
treatment
paradigms
altogether
distinct
from
current
approaches.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Май 2, 2024
Detecting
early-stage
esophageal
squamous
cell
carcinoma
(ESCC)
and
precancerous
lesions
is
critical
for
improving
survival.
Here,
we
conduct
whole-genome
bisulfite
sequencing
(WGBS)
on
460
cfDNA
samples
from
patients
with
non-metastatic
ESCC
or
matched
healthy
controls.
We
develop
an
expanded
multimodal
analysis
(EMMA)
framework
to
simultaneously
identify
methylation,
copy
number
variants
(CNVs),
fragmentation
markers
in
WGBS
data.
methylation
are
the
earliest
most
sensitive,
detectable
70%
of
ESCCs
50%
lesions,
associated
molecular
subtypes
tumor
microenvironments.
CNVs
features
show
high
specificity
but
linked
late-stage
disease.
EMMA
significantly
improves
detection
rates,
increasing
AUCs
0.90
0.99,
detects
87%
62%
>95%
validation
cohorts.
Our
findings
demonstrate
potential
methylome
early
monitoring
characteristics
ESCC.