Frontiers in Immunology,
Год журнала:
2023,
Номер
14
Опубликована: Дек. 4, 2023
Uveal
melanoma
(UV)
is
a
rare
and
aggressive
with
poor
1-year
survival.
up
to
50%
of
UV
patients
develop
metastases,
mainly
the
liver.
Here,
authors
present
2-deoxy-2-[
Cancers,
Год журнала:
2023,
Номер
15(21), С. 5179 - 5179
Опубликована: Окт. 27, 2023
[18F]-FDG
positron
emission
tomography
with
computed
(PET/CT)
imaging
is
widely
used
to
enhance
the
quality
of
care
in
patients
diagnosed
cancer.
Furthermore,
it
holds
potential
offer
insight
into
synergic
effect
combining
radiation
therapy
(RT)
immuno-oncological
(IO)
agents.
This
achieved
by
evaluating
treatment
responses
both
at
RT
and
distant
tumor
sites,
thereby
encompassing
phenomenon
known
as
abscopal
effect.
In
this
context,
PET/CT
can
play
an
important
role
establishing
timelines
for
RT/IO
administration
monitoring
responses,
including
novel
patterns
such
hyperprogression,
oligoprogression,
pseudoprogression,
well
immune-related
adverse
events.
commentary,
we
explore
incremental
value
combination
IO
precision
solid
tumors,
offering
supplementary
insights
recently
released
joint
guidelines.
Advances in Bioscience and Biotechnology,
Год журнала:
2023,
Номер
14(04), С. 151 - 161
Опубликована: Янв. 1, 2023
Immune
checkpoint
inhibitors
(ICIs),
targeting
programmed
cell
death
protein-1
(PD-1)
and
its
ligand
(PD-L1),
have
changed
the
treatment
history
of
lung
cancer,
especially
in
field
non-small
cancer
(NSCLC).
18F-FDG
PET/CT,
as
a
noninvasive
effective
examination
technique,
reflects
location
functional
information
tumor
lesions
through
metabolic
level
glucose.
Studies
shown
that
PD-L1
may
affect
sugar
metabolism
cells.
Therefore,
PET/CT
can
be
used
to
predict
expression
evaluate
efficacy
immunotherapy.
This
article
mainly
introduces
relationship
between
NSCLC,
advantages
imaging
mechanism
based
on
research
progress
role
response
evaluation
immunotherapy
aiming
provide
reference
for
clinic.
Frontiers in Oncology,
Год журнала:
2023,
Номер
13
Опубликована: Окт. 4, 2023
In
lung
clinical
trials
with
imaging,
blinded
independent
central
review
double
reads
is
recommended
to
reduce
evaluation
bias
and
the
Response
Evaluation
Criteria
Solid
Tumor
(RECIST)
still
widely
used.
We
retrospectively
analyzed
inter-reader
discrepancies
rate
over
time,
risk
factors
for
related
baseline
evaluations,
potential
of
machine
learning
predict
discrepancies.We
five
BICR
patients
on
immunotherapy
or
targeted
therapy
cancer.
Double
1724
involving
17
radiologists
were
performed
using
RECIST
1.1.
evaluated
time
according
four
endpoints:
progressive
disease
declared
(PDD),
date
(DOPD),
best
overall
response
(BOR),
first
(DOFR).
Risk
associated
analyzed,
two
predictive
models
evaluated.At
end
trials,
discrepancy
rates
between
not
different.
On
average,
21.0%,
41.0%,
28.8%,
48.8%
PDD,
DOPD,
BOR,
DOFR,
respectively.
Over
was
higher
DOFR
than
increased
as
trial
progressed,
even
after
accrual
completed.
It
rare
readers
find
any
disease,
less
7%
patients,
at
least
one
reader
selected
non-measurable
only
(NTL).
Often
some
their
target
lesions
(TLs)
NTLs
in
different
organs,
ranges
36.0-57.9%
60.5-73.5%
Rarely
(4-8.1%)
all
TLs
locations.
Significant
depending
endpoint
being
considered.
Prediction
had
a
poor
performance
but
positive
value
80%.
The
classification
obtained
BOR.Predicting
discordance
necessitates
having
knowledge
patient
accrual,
survival,
probability
discordances
time.
cancer
although
are
known,
they
weakly
significant,
ability
from
data
limited.
To
boost
prediction
accuracy,
it
would
be
necessary
enhance
baseline-derived
features
create
new
ones,
considering
other
looking
into
optimal
associations.
Frontiers in Oncology,
Год журнала:
2023,
Номер
13
Опубликована: Ноя. 9, 2023
This
study
aimed
to
elucidate
the
relationship
between
dynamic
genomic
mutation
alteration
and
pseudoprogression
(PsPD)/hyperprogressive
disease
(HPD)
in
immunotherapy-treated
advanced
non-small-cell
lung
cancer
(NSCLC),
provide
clinical
evidence
for
identifying
distinguishing
PsPD
HPD.Patients
with
NSCLC
who
were
treated
anti-PD1
enrolled.
Whole
blood
was
collected
at
baseline
post
image
progression.
Serum
separated
sequenced
using
425-panel
next-generation
sequencing
analysis
(NGS).NGS
revealed
that
not
only
single
gene
mutations
associated
PsPD/HPD
before
treatment,
monitoring
of
whole-blood
genome
spectrum
also
varied
greatly.
Mutational
burden,
allele
frequency%,
relative
circulating
tumor
DNA
abundance
indicated
fold
change
after
progression
much
higher
HPD
group.The
profiles
differed
but
true
patients
HPD.
suggests
whole-genome
profile
as
NGS
can
distinguish
from
more
effectively
than
detection,
providing
a
novel
method
guiding
immune
treatment.
Frontiers in Immunology,
Год журнала:
2023,
Номер
14
Опубликована: Дек. 4, 2023
Uveal
melanoma
(UV)
is
a
rare
and
aggressive
with
poor
1-year
survival.
up
to
50%
of
UV
patients
develop
metastases,
mainly
the
liver.
Here,
authors
present
2-deoxy-2-[