Case Reports in Dermatology,
Journal Year:
2022,
Volume and Issue:
14(1), P. 88 - 92
Published: April 21, 2022
An
increasing
number
of
checkpoint
inhibitor-induced
subacute
cutaneous
lupus
erythematosus
events
have
been
reported.
We
present
the
first
case
nivolumab-induced
discoid
in
a
patient
with
hepatocellular
carcinoma.
The
presents
violaceous
hypopigmented
plaques
on
pinna
bilaterally,
central
hyperpigmentation
posterior
neck,
and
other
face,
forearms,
hands.
For
management,
nivolumab
was
held
for
2
months,
Plaquenil
topical
steroids
were
added.
Nivolumab
resumed
no
further
progression
DLE
lesions
improvement
skin.
It
is
important
to
characterize
side
effects
effectively
manage
them.
Frontiers in Medicine,
Journal Year:
2024,
Volume and Issue:
11
Published: Feb. 1, 2024
Immune
checkpoint
inhibitor
(ICI)
use
has
been
associated
with
numerous
autoimmune
side
effects,
known
as
immune
related
adverse
events
(irAEs).
Cutaneous
irAEs
are
common
and
affect
up
to
50%
of
patients
treated
ICIs.
There
have
an
increasing
number
cases
reported
in
the
literature
regarding
ICI-induced
subacute
cutaneous
lupus
erythematosus
(SCLE).
SCLE
is
important
recognize
it
can
result
a
delayed
and/or
prolonged
skin
reaction
despite
treatment
discontinuation.
We
describe
patient
gastro-esophageal
adenocarcinoma
who
developed
following
one
cycle
nivolumab
treatment.
A
75-year-old
man
presented
our
clinic
new
photo-distributed
rash
composed
oval
scaly
pink
papules
plaques
involving
his
chest
arms.
Despite
topical
corticosteroids,
he
emergency
department
1
week
later
worsening
rash.
Skin
biopsy
showed
vacuolar
interface
pattern,
along
superficial
perivascular
lymphocytic
infiltrate,
consistent
drug
eruption.
The
clinicopathological
presentation
was
SCLE.
Nivolumab
discontinued
due
severity
remitted
systemic
high
potency
steroids,
hydroxychloroquine.
Unfortunately,
intraperitoneal
metastatic
disease,
enrolled
hospice
care.
In
this
paper,
we
highlight
importance
early
identification
irAE.
review
literature,
including
discussion
on
management
also
provided.
Arthritis & Rheumatology,
Journal Year:
2020,
Volume and Issue:
73(4), P. 553 - 565
Published: Nov. 13, 2020
Rheumatologists
increasingly
receive
consults
for
patients
treated
with
immune
checkpoint
inhibitors
(ICIs)
cancer.
ICIs
can
cause
inflammatory
syndromes
known
as
immune‐related
adverse
events
(IRAEs).
Several
rheumatic
IRAEs
have
been
reported,
including
arthritis,
polymyalgia
rheumatica,
and
myositis.
For
who
present
musculoskeletal
symptoms
while
receiving
ICI
therapy,
it
is
important
to
an
algorithm
evaluation.
The
differential
diagnosis
includes
a
range
of
syndromes,
such
crystalline
mechanical
issues,
osteoarthritis,
in
addition
IRAEs.
After
diagnosing
IRAE,
rheumatologists
must
work
the
patient
oncologist
form
treatment
plan.
Treatment
guided
by
severity.
Evidence
management
limited
observational
studies.
Inflammatory
arthritis
rheumatica
are
nonsteroidal
antiinflammatory
drugs
mild
cases,
glucocorticoids
moderate‐to‐severe
sometimes
require
other
disease‐modifying
antirheumatic
drugs.
Myositis
due
be
accompanied
myocarditis
or
myasthenia
gravis.
Glucocorticoids
withholding
usually
required
treat
myositis;
some
severe
myositis
intravenous
immunoglobulin
plasmapheresis.
Further
research
needed
optimize
that
does
not
compromise
antitumor
effect
ICIs.
Expert Review of Clinical Pharmacology,
Journal Year:
2019,
Volume and Issue:
13(1), P. 35 - 42
Published: Nov. 27, 2019
Introduction:
There
is
a
growing
list
of
drugs
implicated
in
inducing
both
subacute
and
chronic
forms
cutaneous
lupus
erythematosus.
It
important
to
recognize
these
order
quickly
treat
patients
with
drug
induced
disease.Areas
covered:
This
paper
reviews
the
current
literature
describing
causing
A
Pubmed
search
was
used
compile
medications
up
August
2019.
new
classes
identified
as
erythematosus,
pathophysiology
disease
process,
recommendations
for
treatment
disease.Expert
opinion:
Many
have
been
lupus,
many
more
continue
be
described
reports.
Further
research
needed
understand
this
phenomenon,
which
will
aid
diagnosis
affected
patients.
Pharmaceuticals,
Journal Year:
2024,
Volume and Issue:
17(2), P. 252 - 252
Published: Feb. 15, 2024
Immune
checkpoint
inhibitors
(ICIs)
are
the
standard
of
care
for
a
growing
number
malignancies.
Unfortunately,
they
associated
with
broad
range
unique
toxicities
that
mimic
presentations
primary
autoimmune
conditions.
These
adverse
events
termed
immune-related
(irAEs),
which
ICI-lupus
erythematosus
(ICI-LE)
constitutes
small
percentage.
Our
review
aims
to
describe
available
literature
on
ICI-LE
and
ICI
treatment
patients
pre-existing
lupus.
Most
diagnoses
had
findings
only
cutaneous
lupus;
four
systemic
lupus
manifestations.
Over
90%
(27
29)
cases
received
anti-PD-1/PDL-1
monotherapy,
1
combination
therapy,
anti-CTLA-4
treatment.
About
three-fourths
(22
29
or
76%)
were
managed
topical
steroids,
13
(45%)
hydroxychloroquine,
10
(34%)
required
oral
corticosteroids.
In
our
case
series,
none
receiving
therapy
cancer
flare
their
lupus,
but
few
de
novo
irAE
manifestations,
all
characterized
as
low-grade.
The
yielded
seven
flares
from
total
27
who
ICI.
manageable
without
need
cessation.
Clinical and Experimental Dermatology,
Journal Year:
2020,
Volume and Issue:
46(2), P. 328 - 337
Published: Sept. 17, 2020
Immune
checkpoint
inhibitors
(ICI)
may
cause
eruptions
resembling
cutaneous
autoimmune
diseases.
There
are
six
cases
of
immunotherapy-associated
subacute
lupus
erythematosus
(SCLE)
in
the
literature.
We
present
details
five
patients
referred
to
Skin
Toxicity
Program
at
Dana-Farber
Cancer
Institute/Brigham
and
Women's
Center
who
developed
de
novo
SCLE-like
eruptions,
along
with
clinicopathological
correlation
highlight
potential
mechanistic
features
important
diagnostic
points.
Two
were
maintained
on
topical
corticosteroids,
antihistamines
photoprotection.
One
had
complete
clearance
two
improvement
addition
hydroxychloroquine.
Four
continued
their
immunotherapy
uninterrupted,
while
one
suspended
for
a
month
before
restarting
full
dose.
Histopathologically,
this
series
illustrates
temporal
evolution
ICI-induced
immune
reactions
SCLE
subtype.
Looking
beyond
universally
lichenoid
infiltrate,
evolving
evident.
hypothesize
that
programmed
death-1
blockade
induce
immunological
recognition
previously
immunologically
tolerated
drug
antigens,
leading
epitope
spreading
phenotype.
American Society of Clinical Oncology Educational Book,
Journal Year:
2020,
Volume and Issue:
40, P. 55 - 70
Published: May 1, 2020
Agents
with
mechanisms
novel
to
breast
cancer
care
have
been
approved
treat
cancer.
These
agents
include
drugs
that
target
cyclin-dependent
kinases,
phosphoinositide
3-kinase
PI3KCA
gene
mutations,
PARP,
checkpoint
regulation,
and
antibody-drug
conjugates.
However,
these
approaches
bring
a
risk
of
toxicities
quite
different
from
those
conventional
cytotoxic
chemotherapy.
Here,
we
review
discuss
related
adverse
events,
particular
attention
endocrine,
pulmonary,
dermatologic
toxicities.
Endocrine
associated
therapies
for
are
distinct
often
present
symptoms
the
specific
hormonal
deficiencies
rarely
excess.
Given
complex
sometimes
irreversible
nature
toxicities,
once
recognized,
transdisciplinary
management
an
endocrinologist
experienced
managing
drug-related
is
encouraged.
Drug-related
pneumonitis
serious
concern
new
targeted
therapies.
Presentation
may
not
be
easily
distinguished,
multidisciplinary
team
approach
can
optimize
patient
care.
Heightened
awareness
crucial
early
detection
treatment.
Management
should
follow
recommendations
provided
by
National
Cancer
Institute
Common
Terminology
Criteria
Adverse
Events
agent-specific
guidelines.
Cutaneous
anticancer
represent
common
poorly
characterized
challenge
patients
Although
our
understanding
effects
continues
improve,
breadth
spans
all
conditions.
Targeted
offer
effective
therapeutic
strategies
but
also
event
profiles.
In
this
era,
it
will
important
both
closely
monitoring
remain
vigilant
emerging
Journal of Dermatological Treatment,
Journal Year:
2021,
Volume and Issue:
33(3), P. 1691 - 1695
Published: March 3, 2021
Background
Dermatoses
are
common
and
potentially
serious
complications
of
programmed
cell
death
receptor
PD-1
immune
checkpoint
inhibitor
(anti-PD-1
ICI)
therapy.
Understanding
their
incidence
is
necessary
to
support
clinical
awareness,
diagnosis,
management.Objective
To
examine
the
odds
reported
non-cancerous
dermatoses
in
setting
anti-PD-1
ICI
therapy.Methods
Cross-sectional
study
(pembrolizumab
or
nivolumab)
treated
patients
at
a
tertiary
healthcare
institution.
Selected
dermatologic
events
following
immunotherapy
were
identified
electronic
medical
record.
Comparator
arm
that
developed
these
same
without
receiving
therapy.Results
There
13.7%
(254/1857)
one
28
dermatoses.
Compared
with
general
population,
had
greater
risk
for
development
mucositis
(OR
65.7,
95%
CI
35.0–123.3),
xerostomia
11.9,
8.4–16.8),
pruritus
(11.3,
8.9–14.3),
lichen
planus/lichenoid
dermatitis
10.7,
5.6–20.7).Conclusions
We
report
frequency
encountered
therapy,
both
(pruritus,
rash,
vitiligo)
uncommon
(scleroderma,
urticaria).
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(5), P. 4580 - 4580
Published: Feb. 26, 2023
Immunotherapy
in
oncology
is
replacing
traditional
therapies
due
to
it
specific
action
and
limited
side
effects.
Despite
the
high
efficacy
of
immunotherapy,
effects
such
as
bacterial
infection
have
been
reported.
Bacterial
skin
soft
tissue
infections
represent
one
most
important
differential
diagnoses
patients
presenting
with
reddened
swollen
tissue.
Among
these
infections,
cellulitis
(phlegmon)
abscesses
are
frequent.
In
cases,
occur
locally
possible
contiguous
spread,
or
a
multifocal
manifestation,
especially
immunocompromised
patients.
Herein,
we
report
case
pyodermitis
an
district
patient
treated
nivolumab
for
non-small
cell
lung
cancer.
A
64-year-old,
smoker
male
showed
cutaneous
lesions
at
different
evolution
level
left
arm,
all
tattooed
area,
phlegmon
two
ulcerated
lesions.
Microbiological
cultures
gram
staining
revealed
caused
by
methicillin-susceptible
but
erythromycin-resistant
(ER-R),
clindamycin-resistant
(CL-R),
gentamicin-resistant
(GE-R)
Staphylococcus
aureus
strain.
immunotherapy
becoming
milestone
oncologic
treatment,
more
than
spectrum
immune-mediated
toxicities
agents
needs
be
investigated.
This
highlights
importance
considering
lifestyle
background
before
starting
cancer
emphasis
on
pharmacogenomics
possibility
modified
microbiota
predisposing
PD-1
inhibitors.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Dec. 8, 2023
The
anti-programmed
cell
death
protein
1
(PD-1)
antibody
cemiplimab
has
shown
promising
results
in
the
treatment
of
unresectable
or
metastatic
squamous
carcinoma,
however,
frequently
leads
to
immune-related
adverse
events
limiting
therapy
efficacy.
Although
cutaneous
side
effects
are
common,
only
very
few
cases
lupus
erythematosus
have
been
reported
under
anti-PD-1
immunotherapy.
So
far,
no
case
described
with
cemiplimab.
For
first
time,
we
report
a
patient
advanced
who
developed
clinical
and
histological
findings
sun-exposed
skin
that
were
consistent
anti-SS-A/Ro
antibody-positive
subacute
(SCLE)
Additionally,
laboratory
chemical
analyses
revealed
severe
hepatitis
without
symptoms.
Both,
SCLE
hepatitis,
resolved
after
administration
topical
systemic
steroids
discontinuation
therapy.
Treatment
can
be
associated
appearance
areas.
Application
glucocorticoids
lead
rapid
resolution
eruptions.
Moreover,
our
illustrates
possibility
simultaneously
occurring
events.
This
highlights
importance
additional
diagnostics
avoid
overlooking