Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(4), P. 921 - 921
Published: April 21, 2024
Current
management
of
non-metastatic
muscle
invasive
bladder
cancer
(MIBC)
includes
radical
cystectomy
and
cisplatin-based
neoadjuvant
chemotherapy
(NAC),
offers
a
5-year
survival
rate
approximately
50%
is
associated
with
significant
toxicities.
A
growing
body
evidence
supports
the
role
liquid
biopsies
including
circulating
tumour
DNA
(ctDNA)
as
prognostic
predictive
marker
that
could
stratify
patients
according
to
individualised
risk
progression/recurrence.
Detectable
ctDNA
levels
prior
have
been
shown
be
correlated
higher
recurrence
worse
overall
prognosis
after
cystectomy.
In
addition,
status
NAC/neoadjuvant
immunotherapy
pathological
response
these
treatments,
persistently
detectable
being
residual
at
Finally,
post-cystectomy
disease
relapse
disease-free
(DFS)
(OS)
might
identify
population
benefit
from
adjuvant
immunotherapy.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(6), P. 3105 - 3105
Published: March 7, 2024
Tumors
intricately
shape
a
highly
immunosuppressive
microenvironment,
hampering
effective
antitumor
immune
responses
through
diverse
mechanisms.
Consequently,
achieving
optimal
efficacy
in
cancer
immunotherapy
necessitates
the
reorganization
of
tumor
microenvironment
and
restoration
responses.
Bladder
cancer,
ranking
as
second
most
prevalent
malignant
urinary
tract,
presents
formidable
challenge.
Immunotherapeutic
interventions
including
intravesical
BCG
checkpoint
inhibitors
such
atezolizumab,
avelumab,
pembrolizumab
have
been
implemented.
However,
substantial
unmet
need
persists
majority
bladder
patients
across
all
stages
do
not
respond
adequately
to
immunotherapy.
establishes
that
can
actively
hinder
an
efficient
anti-tumor
response.
A
deeper
understanding
evasion
mechanisms
will
aid
suppressing
recurrence
identifying
viable
therapeutic
targets.
This
review
seeks
elucidate
specific
explore
novel
pathways
molecular
targets
might
circumvent
resistance
Cancers,
Journal Year:
2024,
Volume and Issue:
16(12), P. 2280 - 2280
Published: June 20, 2024
CtDNA
is
emerging
as
a
non-invasive
clinical
detection
method
for
several
cancers,
including
genitourinary
(GU)
cancers
such
prostate
cancer,
bladder
and
renal
cell
carcinoma
(RCC).
assays
have
shown
promise
in
early
of
GU
providing
prognostic
information,
assessing
real-time
treatment
response,
detecting
residual
disease
relapse.
The
ease
obtaining
“liquid
biopsy”
from
blood
or
urine
enhances
its
potential
to
be
used
biomarker.
Interrogating
these
biopsies”
ctDNA
can
then
detect
common
cancer
mutations,
novel
genomic
alterations,
epigenetic
modifications.
has
undergone
investigation
numerous
trials,
which
could
address
needs
instance,
earlier
RCC,
therapeutic
response
prediction
castration-resistant
monitoring
recurrence
cancers.
utilization
liquid
biopsy
analysis
provides
promising
advancing
precision
medicine
within
the
field
The Oncologist,
Journal Year:
2024,
Volume and Issue:
29(9), P. 731 - 737
Published: Aug. 2, 2024
In
the
recent
decade,
analysis
of
circulating
tumor
DNA
(ctDNA)
has
improved
cancer
care
by
allowing
for
rapid
detection
actionable
molecular
targets.
A
new
generation
tests
is
now
becoming
available
commercially.
These
are
characterized
a
superior
limit
0.01%
vaF
or
better,
radiologically
occult
residual
disease
(MRD).
MRD
have
potential
to
revolutionize
neoadjuvant
and
adjuvant
treatment.
addition,
these
can
be
used
as
markers
assess
response.
We
reviewed
current
evidence
use
high-sensitivity
assays
with
particular
focus
on
genitourinary
tumors.
Multiple
studies
been
reported
in
urothelial,
renal,
recently
testicular
carcinoma.
find
that
sensitivity
varies
across
types
setting
may
reach
high
100%
urothelial
cancer.
Specificity
tumor-informed
appears
preserved
(98%-100%).
Several
trials
prospectively
validating
testing
biomarker
integral
studies,
mainly
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 21, 2025
Bladder
cancer
is
a
malignant
tumor
with
high
global
incidence
and
recurrence
rate.
Traditional
diagnostic
methods,
such
as
cystoscopy
urine
cytology,
have
limitations
in
sensitivity
specificity,
particularly
detecting
low-grade
bladder
cancer.
Circulating
DNA
(ctDNA)
offers
non-invasive
alternative,
reflecting
genetic
characteristics
through
blood
samples.
It
demonstrates
repeatability,
making
it
promising
tool
for
early
detection,
monitoring,
treatment
evaluation.
Clinical
studies
shown
that
ctDNA
not
only
detects
burden
but
also
captures
dynamic
mutations,
aiding
personalized
strategies.
Despite
its
potential,
clinical
implementation
of
faces
challenges,
including
optimization
detection
techniques,
standardization,
the
cost
testing.
This
paper
explores
role
advancing
diagnosis
treatment,
focus
on
refining
application
guiding
future
research
toward
improved
patient
outcomes.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 29, 2025
Background
Circulating
tumor
DNA
(ctDNA)
has
emerged
as
a
novel
biomarker
with
the
advantages
of
being
non-invasive
and
enabling
dynamic
monitoring,
providing
significant
clinical
insights
into
prognosis
management
malignancies.
However,
its
prognostic
role
in
patients
urothelial
carcinoma
(UC)
receiving
immune
checkpoint
inhibitors
(ICI)
remains
controversial.
This
study
aims
to
systematically
review
perform
meta-analysis
evaluate
significance
ctDNA
levels
this
specific
patient
population.
Methods
We
conducted
comprehensive
search
PubMed,
Cochrane
Library,
CNKI,
EMBASE
databases
include
studies
published
up
November
14,
2024,
assessing
value
UC
treated
ICI.
Fixed-effects
or
random-effects
models
were
used
association
between
overall
survival
(OS),
progression-free
(PFS)/disease-free
(DFS).
Funnel
plots,
Begg’s
test,
Egger’s
test
employed
assess
publication
bias.
Results
Nine
from
eight
articles,
comprising
total
862
(ICIs),
included
meta-analysis.
Seven
investigated
baseline
circulating
status
outcomes.
Compared
without
detectable
ctDNA,
those
elevated
exhibited
significantly
shorter
survival/disease-free
(PFS/DFS)
(HR
=
2.75,
95%
CI
1.36-5.58,
P
0.005),
though
no
statistically
difference
was
observed
(OS)
2.08,
0.83-5.24,
0.119).
Additionally,
we
evaluated
dynamics
during
ICI
therapy.
A
decline
clearance
associated
improved
outcomes
(OS:
HR
0.10,
0.02-0.47,
0.004;
PFS/DFS:
0.27,
0.16-0.45,
<
0.001).
Conclusions
demonstrates
that
is
PFS
DFS
undergoing
Moreover,
changes
are
strongly
correlated
OS
PFS/DFS.
Therefore,
serves
valuable
tool
for
pre-treatment
diagnostic
assessment
stratification
plays
crucial
monitoring
treatment
response
tracking
disease
progression
throughout
Systematic
registration
www.inplasy.com
,
identifier
INPLASY202520058.
Journal of Clinical Oncology,
Journal Year:
2024,
Volume and Issue:
42(35), P. 4196 - 4205
Published: Sept. 6, 2024
PURPOSE
To
evaluate
the
activity
and
safety
of
nivolumab
with
nab-paclitaxel
as
neoadjuvant
therapy,
followed
by
radical
cystectomy
(RC)
postsurgical
adjuvant
in
patients
muscle-invasive
bladder
cancer
(MIBC).
PATIENTS
AND
METHODS
Eligible
had
an
Eastern
Cooperative
Oncology
Group
performance
status
≤1
a
T2-4aN0-1M0
stage
>50%
urothelial
carcinoma
histology
were
ineligible
for
or
refused
cisplatin-based
chemotherapy.
Patients
received
four
cycles
360
mg
once
every
3
weeks
+
125
mg/m
2
on
days
1
8,
weeks,
RC,
then
×
13
cycles.
The
primary
end
point
was
pathologic
complete
response
(CR)
rate
(ypT0N0).
Secondary
points
major
(ypT≤1N0),
safety,
event-free
survival
(EFS),
overall
survival.
RESULTS
Thirty-one
enrolled
from
December
2021
to
June
2023;
19
(61.3%)
cT2
stage,
two
(6.5%)
N1
16
(51.6%)
variant
histology.
Five
(16.1%)
less
than
full
courses
treatment
because
treatment-related
adverse
events
(TRAEs).
Grade
3/4
TRAEs
occurred
eight
(25.8%).
Twenty-eight
underwent
three
RC
after
evidence
clinical
CR
redo
transurethral
resection
tumor
(reTURBT).
trial
met
its
point:
10
(32.3%;
95%
CI,
16.7
51.4)
achieved
ypT0N0
response.
By
including
those
who
reTURBT,
22
(70.9%;
55
87)
ypT≤1N0-x
After
median
follow-up
12
months
(range,
5-22),
disease
relapse
surgery.
12-month
EFS
89.8%
(95%
79.5
100).
CONCLUSION
our
knowledge,
first
results
NURE-Combo
suggest
that
this
combination
could
expand
therapeutic
opportunities
immune-chemotherapy
MIBC.
Cancers,
Journal Year:
2024,
Volume and Issue:
16(7), P. 1247 - 1247
Published: March 22, 2024
Melanoma
treatment
is
leading
the
neo-adjuvant
systemic
(NAS)
therapy
field.
It
hypothesized
that
having
entire
tumor
in
situ,
with
all
of
heterogeneous
antigens,
allows
patient’s
immune
system
to
have
a
broader
response
its
shapes
and
forms.
This
translates
into
higher
clinical
efficacy.
Another
benefit
NAS
potentially
includes
identifying
patients
who
favorable
response,
which
could
offer
an
opportunity
for
de-escalation
extent
surgery
need
adjuvant
radiotherapy
and/or
therapy,
as
well
tailoring
follow-up
terms
frequency
visits
cross-sectional
imaging.
In
this
paper,
we
will
review
rationale
resectable
metastatic
melanoma
results
obtained
so
far,
both
immunotherapy
BRAF/MEKi
discuss
assessment
interpretation,
toxicity
surgical
considerations.
All
trials
been
reported
up
now
investigator-initiated
phase
I/II
either
single-agent
anti-PD-1,
combination
anti-CTLA-4
anti-PD-1
or
BRAF/MEK
inhibition.
The
good
but
are
especially
encouraging
immunotherapies,
showing
high
durable
recurrence-free
survival
rates.
Combination
seems
superior,
rate
pathologic
responses,
particularly
major
(MPR
=
complete
[pCR]
+
near-pCR
[max
10%
viable
cells])
60%
vs.
25–30%.
SWOG
S1801
trial
has
recently
shown
23%
improvement
event-free
(EFS)
after
2
years
pembrolizumab
when
giving
3
doses
15
versus
18
only.
community
keen
see
first
(expected
2024)
NADINA
(NCT04949113),
randomized
between
two
courses
ipilimumab
nivolumab,
followed
by
response-driven
regimen
follow-up.
We
on
eve
immunotherapy,
becoming
novel
standard
care
macroscopic
stage
III
melanoma.
International Journal of Surgery,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 3, 2024
Circulating
tumor
DNA
(ctDNA)
has
emerged
as
a
noninvasive
technique
that
provides
valuable
insights
into
molecular
profiles
and
disease
management.
This
study
aimed
to
evaluate
the
prognostic
significance
of
circulating
in
urothelial
carcinoma
(UC)
through
systematic
review
meta-analysis.