Journal of Experimental & Clinical Cancer Research,
Journal Year:
2024,
Volume and Issue:
43(1)
Published: Dec. 23, 2024
Abstract
Ductal
carcinoma
in
situ
(DCIS)
is
a
noninvasive
breast
disease
that
variably
progresses
to
invasive
cancer
(IBC).
Given
the
unpredictability
of
this
progression,
most
DCIS
patients
are
aggressively
managed
similar
IBC
patients.
Undoubtedly,
treatment
paradigm
places
many
at
risk
overtreatment
and
its
significant
consequences.
Historically,
prognostic
modeling
has
included
assessment
clinicopathological
features
genomic
markers.
Although
these
provide
valuable
insights
into
tumor
biology,
they
remain
insufficient
predict
which
will
progress
IBC.
Contemporary
work
begun
focus
on
microenvironment
surrounding
ductal
cells
for
molecular
patterns
might
progression.
In
review,
extracellular
alterations
occurring
with
malignant
transformation
from
detailed.
Not
only
do
changes
collagen
abundance,
organization,
localization
mediate
transition
IBC,
but
also
discrete
post-translational
regulation
fibers
understood
promote
invasion.
Other
matrix
proteins,
such
as
metalloproteases,
decorin,
tenascin
C,
have
been
characterized
their
role
further
demonstrate
value
matrix.
Importantly,
proteins
influence
immune
fibroblasts
toward
pro-tumorigenic
phenotypes.
Thus,
progressive
play
key
invasion
promise
development.
Multidisciplinary Reviews,
Journal Year:
2025,
Volume and Issue:
8(7), P. 2025218 - 2025218
Published: Feb. 7, 2025
In
the
area
of
theragnostics,
use
artificial
intelligence
(AI)
is
supporting
personalised
medicine
methods
that
merge
therapeutic
and
diagnostic
techniques,
which
causing
sector
to
undergo
a
transition.
An
analysis
historical
backdrop,
current
condition,
promise
intelligence-enhanced
theragnostic
systems
presented
in
this
article.
We
investigate
underlying
ideas
intelligence,
such
as
machine
learning,
deep
neural
networks,
well
their
applications
variety
medical
fields,
including
cancer,
pathology,
imaging,
cardiology,
hypertension
control,
diabetes
management.
The
ability
integrate
wide
information,
recognise
trends,
enable
real-time
decision-making
patient
monitoring
all
illustrate
competency.
It
possible
digital
twins,
make
adaptive
learning
algorithms
dynamic
virtual
models,
might
be
used
optimise
treatment
regimens
anticipate
course
illness.
Important
prospects
for
advancement
biomedical
research
therapy
are
by
biochip
technology
driven
intelligence.
This
includes
gene
chips,
organ-on-a-chip
systems,
biosensors.
However,
there
number
obstacles
must
overcome
before
can
effectively
theragnostics.
These
include
data
security,
privacy,
algorithmic
biases,
legal
frameworks,
acceptability.
vital,
order
realise
full
potential
AI-driven
address
these
constraints
means
extensive
validation,
diversified
datasets,
explainable
clear
communication.
anticipated
synergistic
combination
theragnostics
will
revolutionise
precision
continues
advance.
it
more
accurate
diagnoses,
achieve
tailored
therapeutics,
better
outcomes.
npj Precision Oncology,
Journal Year:
2023,
Volume and Issue:
7(1)
Published: Nov. 15, 2023
Breast
cancer
(BC)
grade
is
a
well-established
subjective
prognostic
indicator
of
tumour
aggressiveness.
Tumour
heterogeneity
and
assessment
result
in
high
degree
variability
among
observers
BC
grading.
Here
we
propose
an
objective
Haematoxylin
&
Eosin
(H&E)
image-based
marker
for
early-stage
luminal/Her2-negative
BReAst
CancEr
that
term
as
the
BRACE
marker.
The
proposed
derived
from
AI
based
at
detailed
level
using
power
deep
learning.
ability
validated
two
well-annotated
cohorts
(Cohort-A/Nottingham:
n
=
2122
Cohort-B/Coventry:
311)
on
luminal/HER2-negative
patients
treated
with
endocrine
therapy
long-term
follow-up.
able
to
stratify
both
distant
metastasis
free
survival
(p
0.001,
C-index:
0.73)
specific
<
0.0001,
0.84)
showing
comparable
prediction
accuracy
Nottingham
Prognostic
Index
Magee
scores,
which
are
manual
histopathological
assessment,
identify
luminal
may
be
likely
benefit
adjuvant
chemotherapy.
Breast Cancer Research and Treatment,
Journal Year:
2024,
Volume and Issue:
206(1), P. 163 - 175
Published: April 9, 2024
To
evaluate
the
Stratipath
Breast
tool
for
image-based
risk
profiling
and
compare
it
with
an
established
prognostic
multigene
assay
in
a
real-world
case
series
of
estrogen
receptor
(ER)-positive
human
epidermal
growth
factor
2
(HER2)-negative
early
breast
cancer
patients
categorized
as
intermediate
based
on
classic
clinicopathological
variables
eligible
chemotherapy.
npj Breast Cancer,
Journal Year:
2024,
Volume and Issue:
10(1)
Published: June 15, 2024
Abstract
Given
high
costs
of
Oncotype
DX
(ODX)
testing,
widely
used
in
recurrence
risk
assessment
for
early-stage
breast
cancer,
studies
have
predicted
ODX
using
quantitative
clinicopathologic
variables.
However,
such
models
incorporated
only
small
cohorts.
Using
a
cohort
patients
from
the
National
Cancer
Database
(NCDB,
n
=
53,346),
we
trained
machine
learning
to
predict
low-risk
(0-25)
or
high-risk
(26-100)
estrogen
receptor
(ER)/progesterone
(PR)/Ki-67
status,
ER/PR
status
alone,
and
no
features.
Models
were
externally
validated
on
diverse
970
(median
follow-up
55
months)
accuracy
prediction
recurrence.
Comparing
area
under
receiver
operating
characteristic
curve
(AUROC)
held-out
set
NCDB,
incorporating
(AUROC
0.78,
95%
CI
0.77–0.80)
ER/PR/Ki-67
0.81,
0.80–0.83)
outperformed
non-quantitative
model
0.70,
0.68–0.72).
These
results
preserved
validation
cohort,
where
0.87,
0.81–0.93,
p
0.009)
0.86,
0.80–0.92,
0.031)
significantly
0.80,
0.73–0.87).
high-sensitivity
rule-out
threshold,
non-quantitative,
identified
35%,
30%
43%
as
cohort.
Of
these
patients,
fewer
than
3%
had
at
5
years.
may
help
identify
who
can
forgo
genomic
testing
initiate
endocrine
therapy
alone.
An
online
calculator
is
provided
further
study.
EBioMedicine,
Journal Year:
2024,
Volume and Issue:
107, P. 105276 - 105276
Published: Aug. 27, 2024
Deployment
and
access
to
state-of-the-art
precision
medicine
technologies
remains
a
fundamental
challenge
in
providing
equitable
global
cancer
care
low-resource
settings.
The
expansion
of
digital
pathology
recent
years
its
potential
interface
with
diagnostic
artificial
intelligence
algorithms
provides
an
opportunity
democratize
personalized
medicine.
Current
workstations,
however,
cost
thousands
hundreds
dollars.
As
incidence
rises
many
low-
middle-income
countries,
the
validation
implementation
low-cost
automated
tools
will
be
crucial
helping
healthcare
providers
manage
growing
burden
cancer.
MedComm,
Journal Year:
2024,
Volume and Issue:
5(11)
Published: Oct. 20, 2024
Abstract
Cancer
is
a
leading
cause
of
morbidity
and
mortality
worldwide,
an
increase
in
incidence
estimated
the
next
future,
due
to
population
aging,
which
requires
development
highly
tolerable
low‐toxicity
cancer
treatment
strategies.
The
use
nanotechnology
tailor
treatments
according
genetic
immunophenotypic
characteristics
patient's
tumor,
allow
its
targeted
release,
can
meet
this
need,
improving
efficacy
minimizing
side
effects.
Nanomedicine‐based
approach
for
diagnosis
rapidly
evolving
field.
Several
nanoformulations
are
currently
clinical
trials,
some
have
been
approved
marketed.
However,
their
large‐scale
production
still
hindered
by
in‐depth
debate
involving
ethics,
intellectual
property,
safety
health
concerns,
technical
issues,
costs.
Here,
we
survey
key
approaches,
with
specific
reference
organ‐on
chip
technology,
cutting‐edge
tools,
such
as
CRISPR/Cas9
genome
editing,
through
nanosystems
needs
personalized
diagnostics
therapy
patients.
An
update
provided
on
nanopharmaceuticals
marketed
those
undergoing
trials.
Finally,
discuss
emerging
avenues
field
challenges
be
overcome
transfer
nano‐based
precision
oncology
into
daily
life.