Therapeutics and Clinical Risk Management,
Journal Year:
2022,
Volume and Issue:
Volume 18, P. 901 - 912
Published: Sept. 1, 2022
To
provide
benchmarks
for
further
studies
of
solitary
fibrous
tumor/hemangiopericytoma
(SFT/HPC)
the
central
nervous
system
(CNS),
we
investigated
association
baseline
demographic,
clinico-pathologic,
and
treatment
factors
with
outcomes
in
those
treated
at
our
center.We
conducted
a
retrospective,
cohort
analysis
patients
SFT/HPC
University
Washington
1990-2020.
Kaplan-Meier
univariable
Cox
analyses
assessed
relationships
between
variables
local
or
global
CNS
recurrence,
extraneural
progression-free
survival
(PFS)
overall
(OS).Among
34
eligible
patients,
median
duration
follow-up
was
79
months
(range
13-318
months).
Local
recurrence
occurred
81
m
(95%
CI
48-151)
47-112),
respectively.
Extraneural
metastases
248
180-Not
Reached)
only
grade
3
tumors.
Median
PFS
OS
were
76
CI:
47-109
months)
210
131-306
months),
Univariable
showed
that
age
diagnosis
associated
(p
=
0.01)
relapse
0.01),
0.03).
Gross
total
resection
decreased
0.02)
improved
0.03);
peri-operative
radiation
0.02).Following
microsurgical
SFT/HPC,
is
common
age,
extent
resection,
adjuvant
radiation.
occurs
some
patients.
Delayed
time-to-initial
justifies
prolonged
surveillance,
but
optimal
approaches
have
not
been
defined.
Clinical Chemistry,
Journal Year:
2024,
Volume and Issue:
70(1), P. 49 - 59
Published: Jan. 1, 2024
Abstract
Background
There
is
accumulating
evidence
supporting
the
clinical
use
of
circulating
tumor
DNA
(ctDNA)
in
solid
tumors,
especially
different
types
gastrointestinal
cancer.
As
such,
appraisal
current
and
potential
utility
ctDNA
needed
to
guide
clinicians
decision-making
facilitate
its
general
applicability.
Content
In
this
review,
we
firstly
discuss
considerations
surrounding
specimen
collection,
processing,
storage,
analysis,
which
affect
reporting
interpretation
results.
Secondly,
evaluate
a
selection
studies
on
colorectal,
esophago-gastric,
pancreatic
cancer
determine
level
for
disease
screening,
detection
molecular
residual
(MRD)
recurrence
during
surveillance,
assessment
therapy
response,
guiding
targeted
therapy.
Lastly,
highlight
limitations
future
directions.
Summary
Current
promising
but
varies
depending
specific
role
type.
Larger
prospective
trials
are
validate
aspects
utility,
standardization
collection
protocols,
analytical
assays,
guidelines
should
be
considered
wider
Oncology Reports,
Journal Year:
2023,
Volume and Issue:
49(5)
Published: April 12, 2023
Circulating
tumor
DNA
(ctDNA)
has
emerged
as
a
promising
biomarker
of
minimal
residual
disease
(MRD)
in
solid
tumors.
There
is
increasing
evidence
to
suggest
that
the
detection
ctDNA
following
curative‑intent
treatments
high
potential
anticipating
future
relapse
various
Multiple
liquid
biopsy
technical
approaches
and
commercial
platforms,
including
tumor‑informed
tumor‑agnostic
assays,
have
been
developed
for
ctDNA‑based
MRD
Accurate
analysis
remains
critical
challenge
due
very
low
concentration
peripheral
blood
samples,
particularly
cancer
patients
surgery
or
treatment.
The
present
review
summarizes
current
key
can
be
used
analyze
surveillance
tumors
provides
brief
update
on
assays
platforms
available
detection.
date
supporting
types
also
reviewed.
In
addition,
biological
variables
considerations
pre‑analytical
analytical
steps
associated
with
are
discussed.
Technology in Cancer Research & Treatment,
Journal Year:
2025,
Volume and Issue:
24
Published: Jan. 1, 2025
The
management
of
early-stage
colon
cancer
involves
surgical
resection
the
primary
tumor
with
or
without
chemotherapy,
depending
on
pathological
staging.
benefit
adjuvant
chemotherapy
for
stage
II
and
III
is
approximately
5%
15%,
indicating
need
optimization
risk
stratification
patient
selection.
Several
studies
have
revealed
that
current
clinicopathological
factors
lack
precision.
Circulating
DNA
(ctDNA)
cell-free
originating
from
cells
can
be
detected
even
in
absence
radiologically
detectable
disease
among
patients
cancer.
Recent
cohort
ctDNA
one
most
significant
prognostic
cancer,
surpassing
clinical
factors.
Prospective
also
suggest
there
may
a
predictive
role
decision
consideration
therapy.
Currently,
randomized
trials
are
enrolling
to
better
define
this
role.
In
review
article,
we
recent
literature
its
We
elaborate
future
utility
practice
unmet
research
optimize
currently
available
assays.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 28, 2025
Abstract
Purpose
While
circulating
tumor
DNA
(ctDNA)
is
a
promising
biomarker
for
minimal
residual
disease
(MRD)
detection
in
head
and
neck
squamous
cell
carcinoma
(HNSCC),
more
sensitive
assays
are
needed
accurate
MRD
at
clinically-relevant
timepoints.
Ultrasensitive
immediately
after
surgery
could
guide
adjuvant
therapy
decisions,
but
early
ctDNA
dynamics
poorly
understood.
Experimental
Design
We
applied
MAESTRO,
whole-genome,
tumor-informed,
mutation-enrichment
sequencing
assay,
pooled
testing
format
called
MAESTRO-Pool,
to
plasma
samples
from
HNSCC
patients
collected
during
surveillance.
evaluated
whether
predict
outcomes.
Results
Among
24
predominantly
HPV-independent
(95.8%)
patients,
rapid
clearance
occurred
by
the
first
postoperative
sample
(1-3
days
postoperatively)
9
without
an
event
(recurrence
or
death).
13/15
with
were
MRD+
(PPV
=
92.9%;
NPV
80%)
median
fraction
(TFx)
of
54
ppm
(range
6-1,177
ppm).
In
last
immediate
window,
8/13
10/13
had
TFx
below
100
ppm,
respectively,
limit
leading
commercial
assays.
Early
correlated
worse
overall
survival
(HR
8.3;
95%
CI:
1.1-66.1;
P
0.02)
event-free
27.4;
3.5-214.5;
<
0.0001)
independent
high-risk
pathology.
Conclusions
Immediate
MAESTRO
was
predictive
recurrence
death.
Given
ultralow
TFxs
observed,
ultrasensitive
will
be
essential
reliable
timepoints
enable
personalized
decision-making
HNSCC.
Cancer Treatment and Research Communications,
Journal Year:
2024,
Volume and Issue:
39, P. 100802 - 100802
Published: Jan. 1, 2024
Reliable
biomarkers
are
needed
to
identify
tumor
recurrence
of
non-small
cell
lung
cancer
(NSCLC)
patients
after
chemoradiotherapy
(CRT)
with
curative
intent.
This
could
improve
consolidation
therapy
progressing
patients.
However,
the
approach
existing
studies
has
limited
transferability
clinic.
A
retrospective
analysis
135
plasma
samples
from
56
inoperable
NSCLC
who
received
CRT
intent
was
performed.
Plasma
collected
at
baseline,
first
check-up
(average
1.6
months
post-RT),
and
second
4.5
post-RT)
were
analyzed
by
deep
sequencing
a
commercially
available
personalized
profiling
strategy
(CAPP-Seq)
using
tumor-agnostic
approach.
Detection
circulating
DNA
(ctDNA)
significantly
associated
higher
odds
(OR:
5.4
(CI:
1.1–31),
Fisher's
exact
test:
p-value
=
0.022),
shorter
recurrence-free
survival
(RFS)
(HR:
4.1
1.7–10);
log-rank
9e-04).
In
contrast,
detection
ctDNA
not
2.7
0.67–12),
0.13)
or
RFS
1.5
0.67–3.3);
0.32).
study
demonstrates
that
can
be
used
minimal
residual
disease
in
kit
Furthermore,
time
point
collecting
sample
decisive
importance
for
prognostic
value
ctDNA.
analysed
treated
Detecting
post-treatment
linked
odds,
indicating
ctDNA's
potential
as
biomarker
identifying
treatment
Importantly,
emphasizes
timing
accurate
results.