British Journal of Dermatology,
Год журнала:
2024,
Номер
191(3), С. 465 - 467
Опубликована: Май 16, 2024
Our
cross-sectional
study
demonstrates
that
there
is
a
high
rate
of
co-trimoxazole-induced
drug
rash
in
patients
treated
for
immune-related
adverse
events,
with
those
developing
appearing
to
have
reduced
survival.
Cancers,
Год журнала:
2024,
Номер
16(7), С. 1440 - 1440
Опубликована: Апрель 8, 2024
The
landscape
of
cancer
treatment
has
undergone
a
significant
transformation
with
the
introduction
Immune
Checkpoint
Inhibitors
(ICIs).
Patients
undergoing
these
treatments
often
report
prolonged
clinical
and
radiological
responses,
albeit
potential
risk
developing
immune-related
adverse
events
(irAEs).
Here,
we
reviewed
discussed
mechanisms
action
ICIs
their
pivotal
role
in
regulating
immune
system
to
enhance
anti-tumor
response.
We
scrutinized
intricate
pathogenic
responsible
for
irAEs,
arising
from
evasion
self-tolerance
checkpoints
due
drug-induced
modulation.
also
summarized
main
manifestations
irAEs
categorized
by
organ
types,
detailing
incidence
associated
factors.
occurrence
is
more
frequent
when
are
combined;
neurological,
cardiovascular,
hematological,
rheumatic
commonly
linked
PD1/PD-L1
inhibitors
cutaneous
gastrointestinal
prevalent
CTLA4
inhibitors.
Due
often-nonspecific
signs
symptoms,
diagnosis
(especially
those
rare
ones)
can
be
challenging.
differential
primary
autoimmune
disorders
becomes
sometimes
intricate,
given
pathophysiological
similarities.
In
conclusion,
considering
escalating
use
ICIs,
this
area
research
necessitates
additional
studies
practical
insights,
especially
development
biomarkers
predicting
toxicities.
addition,
there
need
heightened
education
both
clinicians
patients
understanding
awareness.
Journal of Medical Virology,
Год журнала:
2023,
Номер
95(4)
Опубликована: Апрель 1, 2023
Abstract
Oncolytic
viruses
(OVs)
can
selectively
kill
tumor
cells
without
affecting
normal
cells,
as
well
activate
the
innate
and
adaptive
immune
systems
in
patients.
Thus,
they
have
been
considered
a
promising
measure
for
safe
effective
cancer
treatment.
Recently,
few
genetically
engineered
OVs
developed
to
further
improve
effect
of
elimination
by
expressing
specific
regulatory
factors
thus
enhance
body's
antitumor
immunity.
In
addition,
combined
therapies
other
immunotherapies
applied
clinical.
Although
there
are
many
studies
on
this
hot
topic,
comprehensive
review
is
missing
illustrating
mechanisms
clearance
how
modify
their
effects.
study,
we
provided
OVs.
reviewed
with
including
radiotherapy
CAR‐T
or
TCR‐T
cell
therapy.
The
useful
generalize
usage
OV
Current Oncology,
Год журнала:
2023,
Номер
30(7), С. 6805 - 6819
Опубликована: Июль 18, 2023
Over
the
past
few
decades,
immune
checkpoint
inhibitors
(ICIs)
have
emerged
as
promising
therapeutic
options
for
treatment
of
various
cancers.
These
novel
treatments
effectively
target
key
mediators
pathways.
Currently,
ICIs
primarily
consist
monoclonal
antibodies
that
specifically
block
cytotoxic
T-lymphocyte
antigen
4
(CTLA-4),
programmed
cell
death
1
(PD-1),
death-ligand
(PD-L1),
and
lymphocyte
activation
gene
3
protein
(LAG-3).
Despite
notable
efficacy
in
cancer
treatment,
they
can
also
trigger
immune-related
adverse
events
(irAEs),
which
present
autoimmune-like
or
inflammatory
conditions.
IrAEs
potential
to
affect
multiple
organ
systems,
with
cutaneous
toxicities
being
most
commonly
observed.
Although
irAEs
are
typically
low-grade
severity
usually
be
managed
effectively,
there
cases
where
severe
become
life-threatening.
Therefore,
early
recognition
a
comprehensive
understanding
mechanisms
underlying
crucial
improving
clinical
outcomes
patients.
However,
precise
pathogenesis
remains
unclear.
This
review
focuses
on
skin
manifestations
induced
by
ICIs,
prognosis
related
irAEs,
exploration
involved
irAEs.
Frontiers in Pharmacology,
Год журнала:
2025,
Номер
16
Опубликована: Янв. 31, 2025
Immune
checkpoint
inhibitors
(ICIs)
have
significantly
changed
cancer
therapy,
improving
patient
survival
rates
and
clinical
outcomes.
Nevertheless,
the
use
of
PD-1/PD-L1
can
result
in
immune-related
adverse
events
(irAEs).
This
study
aims
to
investigate
prevalence
associated
risk
factors
irAEs
a
real-world
setting,
as
well
assess
their
effects
on
optimal
therapeutic
A
retrospective
analysis
involved
2523
patients
with
who
received
inpatient
treatment
between
January
2018
December
2022.
We
documented
patients'
demographic
characteristics,
PD-1
or
PD-L1
inhibitors,
modalities,
incidences,
timing,
severity
irAEs,
efficacy
outcomes
by
reviewing
records.
Patients
were
categorized
into
an
group
non-irAEs
group,
former
further
subdivided
multiple
single
irAE
group.
Chi-square
tests
employed
evaluate
differences
baseline
characteristics
groups,
groups.
Additionally,
logistic
regression
was
utilized
identify
linked
irAEs.
Among
eligible
patients,
1096
reported
1802
incidence
43.4%.
individuals,
92.1%
classified
grade
1-2,
while
7.9%
3
higher.
IrAEs
affected
various
organ
systems,
endocrine
toxicity
(17.7%),
hepatic
(17.2%),
hematologic
(11.4%)
being
most
common.
20.5%
experienced
multi-system
The
average
time
for
develop
within
four
cycles.
Significant
gender,
age,
Eastern
Cooperative
Oncology
Group
(ECOG)
Performance
Status
(PS),
comorbidities,
modalities
observed
but
not
Compared
exhibited
higher
objective
response
rate
(ORR)
disease
control
(DCR),
also
showed
ORR
than
indicated
that
occurrence
is
related
ECOG
PS,
modalities.
may
be
better
benefits.
Cancers,
Год журнала:
2025,
Номер
17(2), С. 251 - 251
Опубликована: Янв. 14, 2025
The
landscape
of
available
therapeutic
options
for
treatment
genitourinary
(GU)
cancers
is
expanding
dramatically.
Many
these
treatments
have
distinct,
sometimes
severe,
skin
toxicities
including
morbilliform,
bullous,
pustular,
lichenoid,
eczematous,
psoriasiform,
and
palmoplantar
eruptions.
Pruritus
pigmentation
changes
also
been
noted.
This
review
aims
to
synthesize
dermatologic
events
observed
with
antibody
drug
conjugates,
poly
(ADP-ribose)
polymerase
(PARP)
inhibitors,
androgen
receptor
pathway
tyrosine
kinase
immune
checkpoint
the
combination
agents
used
GU
cancers.
It
provides
a
guide
on
diagnosis
initial
management
rashes
medical
oncologists.
Immune
checkpoint
inhibitors,
now
widely
used
in
treating
various
malignancies,
increase
the
risk
of
autoimmune
reactions
and
immune-related
adverse
events
(irAEs),
with
skin
toxicities
being
most
frequent.
These
agents
enhance
immune
response
against
tumors
by
blocking
suppression
cytotoxic
T
lymphocytes.
Here,
we
report
a
rare
case
generalized
cutaneous
lichen
planus
induced
atezolizumab,
an
inhibitor
administered
for
small
cell
lung
cancer.
After
consulting
oncologist,
opted
to
initiate
isotretinoin
as
first-line
treatment.
Considering
patient's
oncologic
status
multiple
comorbidities,
aimed
avoid
systemic
corticosteroids
due
their
potential
side
effects.
This
was
effectively
managed
low-dose
oral
alongside
high-potency
topical
corticosteroids.
It
emphasizes
need
consider
retinoids
treatment
option
dermatological
conditions
beyond
acne.
Isotretinoin
may
be
beneficial
influencing
cellular
proliferation
promoting
epithelial
differentiation,
though
its
exact
mechanism
remains
uncertain.
Additionally,
it
has
notable
anti-inflammatory
effects
modulates
responses.
In
such
cases,
also
therapeutic
through
synergistic
interaction.
Skin
biopsy
is
one
of
the
most
frequently
performed
diagnostic
measures
in
dermatological
practice.
Depending
on
question,
selection
type
procedure
and
location
can
have
a
considerable
influence
histological
assessment.
disease,
different
aspects
must
be
taken
into
account
for
precise
diagnosis.
This
article
summarizes
these
exanthema,
erythematosquamous
dermatoses,
blistering
diseases,
subcutaneous
inflammatory
processes,
alopecia
with
examples.
Advantages
disadvantages
types
are
also
addressed
neoplastic
diseases.
The
aim
to
draw
attention
difficulties
histopathologic
differential
diagnosis
caused
by
and,
thus,
improve
quality
JAMA Dermatology,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 12, 2025
Importance
Therapies
for
individual
keratinocyte
carcinomas
(KCs)
do
not
prevent
the
onset
of
new
KCs
in
a
field
sun
damage,
and
therefore
KC
burden
remains
unchanged.
Objective
To
investigate
association
immune
checkpoint
inhibitors
(ICIs)
with
changes
cancerization
evaluated
by
number
actinic
keratoses
(AKs)
at
baseline
compared
12
months
after
starting
ICI
therapy.
Design,
Setting,
Participants
This
prospective
cohort
study
was
performed
outpatient
oncology
clinic
single
tertiary
public
hospital
Brisbane,
Australia,
from
April
1,
2022,
to
November
30,
2023.
Consecutive
immunocompetent
adults
therapy
an
inhibitor
programmed
cell
death
1
(PD-1)
or
ligand
(PDL-1)
any
active
cancer,
planned
treatment
duration
least
6
months,
who
exhibited
clinical
AKs
on
their
forearms
were
eligible.
Those
immunosuppression,
concurrent
chemotherapy
radiotherapy,
recent
topical
fluorouracil
use
excluded.
Exposures
Intravenous
therapy,
either
PD-1
PDL-1
without
cytotoxic
T-lymphocyte–associated
protein
4
inhibitor,
determined
treating
oncologist.
Main
Outcomes
Measures
Clinical
counted
photographed
before
3,
6,
numbers
based
histopathology
reports
all
skin
lesions
excised
Participants’
medical
history,
primary
cancer
tumor
response
using
Response
Evaluation
Criteria
Solid
Tumors,
adverse
events
recorded.
Results
A
total
23
participants
recruited,
whom
17
(73.9%)
male,
mean
(SD)
age
69.7
(9.6)
years.
No
withdrew;
however,
died
during
due
disease
progression.
The
AK
significantly
decreased
47.2
(33.8)
14.3
(12.0)
(
P
<
.001).
Younger
patients
(8
[66.7%]
vs
[33.3%];
=
.007)
those
history
blistering
sunburn
(12
[100%]
0;
.005)
more
likely
reduce
65%
greater.
42
after.
cutaneous
squamous
16
5
same
period.
Conclusions
Relevance
pilot
found
that
ICIs
used
associated
significant
reduction
AKs,
suggesting
potential
as
immunopreventive
strategy
high-risk
individuals.
Given
known
effects
other
chemopreventive
agents
KCs,
further
investigation
into
managing
is
required,
especially
considering
toxicity
cost.