Real-World Efficacy and Safety of Anti-PD-1 Antibody Plus Apatinib and Temozolomide for Advanced Acral Melanoma
Jiaran Zhang,
No information about this author
Huichun Tian,
No information about this author
Lili Mao
No information about this author
et al.
Cancer Management and Research,
Journal Year:
2025,
Volume and Issue:
Volume 17, P. 905 - 916
Published: May 1, 2025
The
combination
of
programmed
cell
death-1
(PD-1)
blockade
camrelizumab
plus
apatinib
(an
antiangiogenic
agent)
and
temozolomide
has
displayed
promising
therapeutic
effects
in
patients
with
advanced
acral
melanoma
(AM)
a
non-randomized
Phase
II
clinical
trial
(NCT04397770).
aim
this
retrospective
study
was
to
evaluate
the
efficacy
safety
triplet
regimen
for
AM
real-world
setting.
data
who
received
anti-PD-1
antibody
at
Peking
University
Cancer
Hospital
Institute
between
September
2019
December
2023
were
analyzed.
primary
endpoint
overall
response
rate
(ORR).
secondary
endpoints
included
progression-free
survival
(PFS),
(OS),
disease
control
(DCR),
duration
(DOR),
treatment-related
adverse
events
(TRAEs).
Overall,
250
eligible
analysis.
ORR
38.1%
DCR
92.2%.
median
PFS,
OS,
DOR
8.5,
18.0,
13.2
months,
respectively.
When
used
as
first-line
treatment,
48.1%,
PFS
12.0
OS
24.8
months.
number
lines
therapy
(≥2
lines),
elevated
lactate
dehydrogenase,
presence
brain
or
liver
metastasis
negative
predictors
survival.
92.4%
45.2%
experienced
any-grade
grade
3-4
TRAEs,
This
provides
evidence
that
support
effectiveness
combined
antibody,
treating
AM,
demonstrating
considerable
prolonged
survival,
well
acceptable
tolerability.
Language: Английский
A computed tomography-based radiomics prediction model for BRAF mutation status in colorectal cancer
Baohua Zhou,
No information about this author
Huaqing Tan,
No information about this author
Yuxuan Wang
No information about this author
et al.
Abdominal Radiology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 15, 2025
The
aim
of
this
study
was
to
develop
and
validate
CT
venous
phase
image-based
radiomics
predict
BRAF
gene
mutation
status
in
preoperative
colorectal
cancer
patients.
In
study,
301
patients
with
pathologically
confirmed
were
retrospectively
enrolled,
comprising
225
from
Centre
I
(73
mutant
152
wild-type)
76
II
(36
40
wild-type).
cohort
randomly
divided
into
a
training
set
(n
=
158)
an
internal
validation
67)
7:3
ratio,
while
served
as
independent
external
76).
whole
tumor
region
interest
segmented,
characteristics
extracted.
To
explore
whether
expansion
could
improve
the
performance
objectives,
contour
extended
by
3
mm
study.
Finally,
t-test,
Pearson
correlation,
LASSO
regression
used
screen
out
features
strongly
associated
mutations.
Based
on
these
features,
six
classifiers-Support
Vector
Machine
(SVM),
Decision
Tree
(DT),
Random
Forest
(RF),
Logistic
Regression
(LR),
K-Nearest
Neighbors
(KNN),
Extreme
Gradient
Boosting
(XGBoost)-were
constructed.
model
clinical
utility
evaluated
using
receiver
operating
characteristic
(ROC)
curves,
decision
curve
analysis,
accuracy,
sensitivity,
specificity.
Gender
predictor
unexpanded
RF
model,
constructed
11
imaging
histologic
demonstrated
best
predictive
performance.
For
cohort,
it
achieved
AUC
0.814
(95%
CI
0.732-0.895),
accuracy
0.810,
sensitivity
0.620.
0.798
0.690-0.907),
0.761,
0.609.
0.737
0.616-0.847),
0.658,
0.667.
A
machine
learning
based
can
effectively
mutations
cancer.
optimal
Language: Английский