European Thyroid Journal,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
Immune
checkpoint
inhibitors
(ICIs)
frequently
cause
immune-related
adverse
events
(irAEs),
with
thyroid
irAEs
being
the
most
common
endocrine-related
irAEs.
The
incidence
of
overt
ranged
8.9–22.2%
in
real-world
settings,
typically
triggered
by
antibodies
against
PD-1
and
PD-L1
rarely
anti-CTLA-4
alone.
representative
clinical
course
involves
biphasic
changes
function,
transient
thyrotoxicosis
subsequent
persistent
hypothyroidism.
identified
risk
factors
for
include
presence
autoantibodies,
uptake
18F-FDG-PET,
prior
use
tyrosine
kinase
(TKIs),
high
BMI,
TSH
levels.
There
is
evidence
that
are
associated
good
prognosis,
at
least
non-small
cell
lung
cancer.
Although
features
have
been
well
clarified,
management
strategies
require
further
refinement.
Routine
monitoring
function
every
4
to
6
weeks
during
ICI
therapy
recommended
early
detection
While
generally
requires
observation
only,
hypothyroidism
should
be
promptly
treated
levothyroxine
replacement.
Continuation
feasible
patients
irAEs,
provided
their
overall
health
remains
stable.
However,
these
were
largely
based
on
experience
monotherapy.
As
combination
therapies
developed
as
first-line
treatments,
antitumor
agents
may
modify
For
example,
cytotoxic
can
delay
onset
while
TKIs
often
linked
early-onset
hypothyroidism,
independent
use.
Given
increasing
diversity
complexity
cancer
immunotherapy,
it
essential
vigilantly
screen
Journal of Clinical Oncology,
Год журнала:
2022,
Номер
41(6), С. 1200 - 1212
Опубликована: Окт. 12, 2022
We
present
5-year
results
from
CheckMate
227
Part
1,
in
which
nivolumab
plus
ipilimumab
improved
overall
survival
(OS)
versus
chemotherapy
patients
with
metastatic
non-small-cell
lung
cancer,
regardless
of
tumor
programmed
death
ligand
1
(PD-L1)
status.Adults
stage
IV/recurrent
cancer
without
EGFR
mutations
or
ALK
alterations
and
PD-L1
≥
1%
<
(n
=
1739)
were
randomly
assigned.
Patients
assigned
to
first-line
ipilimumab,
alone,
chemotherapy.
chemotherapy,
End
points
included
exploratory
for
efficacy,
safety,
quality
life.At
a
minimum
follow-up
61.3
months,
OS
rates
24%
14%
(PD-L1
1%)
19%
7%
1%).
The
median
duration
response
was
24.5
6.7
months
19.4
4.8
Among
surviving
5
years,
66%
64%
off
initiating
subsequent
systemic
anticancer
treatment
by
the
time
point.
Survival
benefit
continued
after
discontinuation
because
treatment-related
adverse
events,
rate
39%
(combined
populations).
Quality
life
survivors
treated
similar
that
general
US
population
through
follow-up.
No
new
safety
signals
observed.With
all
immunotherapy
3
increased
survivorship
including
long-term,
durable
clinical
expression.
These
data
support
as
an
effective
cancer.
Frontiers in Immunology,
Год журнала:
2022,
Номер
13
Опубликована: Окт. 11, 2022
Immune
checkpoint
therapy
via
PD-1
antibodies
has
shown
exciting
clinical
value
and
robust
therapeutic
potential
in
practice.
It
can
significantly
improve
progression-free
survival
overall
survival.
Following
surgery,
radiotherapy,
chemotherapy,
targeted
therapy,
cancer
treatment
now
entered
the
age
of
immunotherapy.
Although
immunotherapy
remarkable
efficacy,
it
also
suffers
from
limitations
such
as
irAEs,
cytokine
storm,
low
response
rate,
etc.
In
this
review,
we
discuss
basic
classification,
research
progress,
Besides,
by
combining
resistance
mechanism
with
analysis
combination
give
our
insights
into
development
new
anticancer
strategies.
Frontiers in Immunology,
Год журнала:
2023,
Номер
14
Опубликована: Май 25, 2023
Since
the
first
Immune
Checkpoint
Inhibitor
was
developed,
tumor
immunotherapy
has
entered
a
new
era,
and
response
rate
survival
of
many
cancers
have
also
been
improved.
Despite
success
immune
checkpoint
inhibitors,
resistance
limits
number
patients
who
can
achieve
lasting
response,
immune-related
adverse
events
complicate
treatment.
The
mechanism
(irAEs)
is
unclear.
We
summarize
discuss
mechanisms
action
different
types
their
possible
mechanisms,
describe
strategies
targets
for
prevention
therapeutic
interventions
to
mitigate
them.
Journal of Hematology & Oncology,
Год журнала:
2022,
Номер
15(1)
Опубликована: Июль 7, 2022
The
development
of
combination
immunotherapy
based
on
the
mediation
regulatory
mechanisms
tumor
immune
microenvironment
(TIME)
is
promising.
However,
a
deep
understanding
immunology
must
involve
systemic
environment
(STIE)
which
was
merely
illustrated
previously.
Here,
we
aim
to
review
recent
advances
in
single-cell
transcriptomics
and
spatial
for
studies
STIE,
TIME,
their
interactions,
may
reveal
heterogeneity
responses
as
well
dynamic
changes
essential
treatment
effect.
We
evidence
from
preclinical
clinical
related
significance
overall
survival,
through
different
immunomodulatory
pathways,
such
metabolic
neuro-immunological
pathways.
also
evaluate
interactions
after
local
radiotherapy
or
combined
immunotherapy.
focus
our
lung
cancer,
hepatocellular
carcinoma,
nasopharyngeal
aiming
reshape
STIE
TIME
enhance
efficacy.
Trends in cancer,
Год журнала:
2023,
Номер
9(7), С. 543 - 553
Опубликована: Апрель 27, 2023
Immunotherapy
has
changed
the
treatment
landscape
for
cancer
over
past
decade.
Inhibitors
of
immune
checkpoint
proteins
cytotoxic
T
lymphocyte
antigen
(CTLA)-4,
programmed
death
(PD)-1,
and
PD
ligand
1
(PD-L1)
can
induce
durable
remissions
in
a
subset
patients
with
metastatic
disease.
However,
these
treatments
be
limited
by
inflammatory
toxicities
that
affect
any
organ
system
body
some
cases
life
threatening.
Considerable
progress
been
made
understanding
drivers
as
well
effective
management
strategies.
Further
research
into
molecular
cellular
mechanisms
drive
toxicity
will
enable
better
prediction
development
optimized
therapies
avoid
interfering
antitumor
immunity.
In
this
review,
we
discuss
our
current
from
inhibitors
(ICIs)
propose
optimal
strategies
toxicities.
The Oncologist,
Год журнала:
2022,
Номер
27(3), С. e223 - e232
Опубликована: Янв. 24, 2022
Enfortumab
vedotin
is
a
first-in-class
Nectin-4-directed
antibody-drug
conjugate
approved
by
the
US
Food
and
Drug
Administration
for
treatment
of
patients
with
locally
advanced
or
metastatic
urothelial
cancer
(la/mUC)
previously
treated
platinum-based
chemotherapy
programmed
death
receptor-1/programmed
death-ligand
1
(PD-1/L1)
inhibitor,
la/mUC
who
are
ineligible
cisplatin-based
have
received
one
more
prior
lines
therapy.
only
drug
to
demonstrated
survival
benefit
versus
in
randomized
controlled
trial
PD-1/L1
inhibitor.
The
development
dermatologic
events
following
administration
enfortumab
anticipated
given
expression
Nectin-4
epidermal
keratinocytes
skin
appendages
(eg,
sweat
glands
hair
follicles).
There
potential
rare
but
severe
possibly
fatal
cutaneous
adverse
reactions,
including
Stevens-Johnson
syndrome
toxic
necrosis,
as
described
boxed
warning
prescribing
information
vedotin.
This
manuscript
describes
presumed
pathophysiology
manifestations
reactions
related
vedotin,
presents
recommendations
prevention
treatment,
provide
oncologists
other
healthcare
providers
an
awareness
these
best
anticipate
manage
them.
European Heart Journal,
Год журнала:
2022,
Номер
43(42), С. 4458 - 4468
Опубликована: Авг. 30, 2022
Abstract
Over
the
last
decade
or
so,
there
has
been
a
paradigm
shift
in
oncologic
care
of
patients
with
range
solid
tumour
and
haematologic
malignancies,
away
from
traditional
cytotoxic
chemotherapy
towards
personalized
cancer
treatments,
using
both
targeted
therapy
immunotherapy.
This
contributed
to
remarkable
sustained
increase
number
survivors
longevity
diagnosis.
review
will
focus
on
cardiovascular
effects
immune
checkpoint
inhibitors
present
background
inhibition
for
cancer,
epidemiology,
potential
mechanisms,
insights
into
biology,
diagnostic
therapeutic
approach
cases.
Our
understanding
needs
improve.
However,
evolution
necessarily
be
rapid.
Initial
observations
noted
that
inhibitor
can
lead
fulminant
myocarditis.
Recent
reports
have
expanded
effect
system
include
an
cardiac
dysfunction
without
myocarditis,
arrhythmias,
venous
thromboembolic
disease,
accelerated
atherosclerosis,
atherosclerosis-related
events.
The
association
between
these
events
is
not
only
limited
occurring
within
first
few
weeks
after
starting
but
also
occur
months
years
therapy.
latter
observation
especially
relevance
those
treated
adjuvant
neoadjuvant
There
recognition
currently
approved
therapies
mechanisms
adverse
effects,
who
at
risk,
what
we
do
about
it.