New and Emerging Biologics and Jak Inhibitors for the Treatment of Prurigo Nodularis: A Narrative Review
M.A. Bianco,
F D’Oria,
Costanza Falcidia
и другие.
Medicina,
Год журнала:
2025,
Номер
61(4), С. 631 - 631
Опубликована: Март 29, 2025
Prurigo
nodularis
(PN)
is
a
chronic
dermatological
condition
characterized
by
intensely
pruritic
nodules
resulting
from
repeated
scratching.
Its
pathogenesis
involves
neuroimmune
dysregulation,
inflammatory
cytokines,
and
neural
proliferation.
Conventional
treatments
often
provide
limited
relief,
necessitating
novel
therapeutic
approaches.
This
narrative
review
explores
emerging
biologics
small
molecules
for
PN
treatment,
assessing
their
mechanisms,
efficacy,
safety.
A
comprehensive
literature
search
was
conducted
using
PubMed,
Google
Scholar,
Web
of
Science
relevant
studies
up
to
February
2025.
Additionally,
ongoing
clinical
trials
were
identified
through
ClinicalTrials.gov.
The
terms
included
“prurigo
nodularis”,
“biologic
treatments”,
“monoclonal
antibodies”,
“small
molecules”,
“JAK
inhibitors”.
Among
new
treatment
options,
dupilumab,
an
IL-4
receptor
antagonist,
nemolizumab,
IL-31
inhibitor,
demonstrated
significant
efficacy
in
reducing
pruritus
lesion
severity
patients.
Other
promising
monoclonal
antibodies
include
vixarelimab
(OSMRβ
inhibitor)
barzolvolimab
(KIT
inhibitor).
Small
such
as
JAK
inhibitors
(upadacitinib,
povorcitinib)
also
show
potential
modulating
pathways.
Clinical
highlight
safety,
long-term
benefits.
Emerging
represent
transformative
approach
management,
offering
targeted
therapies
that
address
underlying
immunological
neurological
mechanisms.
Ongoing
research
are
crucial
optimizing
strategies
improving
patient
outcomes.
Язык: Английский
Real-World Effectiveness and Safety of Upadacitinib and Abrocitinib in Moderate-to-Severe Atopic Dermatitis: A 52-Week Retrospective Study
Journal of Clinical Medicine,
Год журнала:
2025,
Номер
14(9), С. 2953 - 2953
Опубликована: Апрель 24, 2025
Background:
Atopic
dermatitis
(AD)
is
a
chronic
pruritic
inflammatory
disease
affecting
children
and
adults.
Upadacitinib
abrocitinib
are
selective
Janus
kinase
1
inhibitors
approved
for
the
treatment
of
moderate-to-severe
AD.
Although
their
efficacy
safety
described
in
phase
3
clinical
trials,
real-world
data
limited.
Objectives:
We
aimed
to
evaluate
effectiveness
upadacitinib
real-life
adult
population
with
AD
throughout
an
extended
observation
period.
Methods:
This
retrospective
observational
study
was
conducted
by
analyzing
from
electronic
records
IRCCS
Humanitas
Research
Hospital
January
2023
December
2024.
Patients
were
administered
either
(15
or
30
mg)
(100
200
mg).
Effectiveness
evaluated
using
clinician-reported
scores
(Investigator
Global
Assessment
[IGA]
Eczema
Area
Severity
Index
[EASI])
patient-reported
outcomes
(peak
pruritus
numerical
rating
scale
[PP-NRS])
at
weeks
8,
16,
32
52.
Statistical
significance
set
probability
value
(p-value)
<
0.05.
Adverse
events
also
collected.
Results:
In
total,
129
patients
included
study,
84
them
reached
52
weeks.
At
week
52,
EASI
75,
90,
100
responses
88.9%,
70.8%,
54.2%
upadacitinib,
100%,
91.7%,
75%
abrocitinib.
An
IGA
score
equal
0
achieved
84.7%
treated
100%
those
receiving
A
four-point
reduction
baseline
PP-NRS
reported
86.1%
83.3%
after
one
year
follow-up.
Conclusions:
Our
showed
comparable
even
higher
terms
compared
phase-3
no
new
concerns,
supporting
Язык: Английский
The Transition of Blood Biomarkers During 96-Week Treatment with Upadacitinib for Atopic Dermatitis: A Real-World Analysis Stratified by Age
Dermatitis,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 29, 2025
Background:
The
transition
of
laboratory
indexes
is
unknown
for
long-term
(2-year)
upadacitinib
treatment
in
atopic
dermatitis
(AD).
Objective:
To
assess
the
96-week
real-world
effects
on
immunoglobulin
E
(IgE),
thymus
and
activation-regulated
chemokine
(TARC),
lactate
dehydrogenase
(LDH),
total
eosinophil
count
(TEC)
Japanese
patients
with
AD,
stratified
by
age
groups
(<18,
18-64,
≥65
years).
Methods:
In
this
prospective,
single-center
study,
received
15
mg
or
30
plus
topical
corticosteroids
from
August
2021
to
November
2024.
Laboratory
(IgE,
TARC,
LDH,
TEC)
clinical
(eczema
area
severity
index,
peak
pruritus-numerical
rating
scale)
were
measured
at
weeks
0,
4,
12,
24,
36,
48,
60,
72,
84,
96.
Results:
Upadacitinib
generated
a
sustained
reduction
until
week
96
all
groups.
TEC
decreased
4
12
remained
below
baseline
Patients
aged
years
maintained
lowest
among
three
Conclusion:
provided
across
parallel
reduced
AD.
may
act
as
potential
biomarker
reflecting
responsiveness
upadacitinib.
Язык: Английский
Treatment of Moderate-to-severe Atopic Dermatitis with Upadacitinib: Results from an Interim Analysis of the TREATgermany Registry
Acta Dermato Venereologica,
Год журнала:
2025,
Номер
105, С. adv42206 - adv42206
Опубликована: Май 21, 2025
Язык: Английский
Drug-Induced Acne in Inflammatory Bowel Disease: A Practical Guide for the Gastroenterologist
The American Journal of Gastroenterology,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 9, 2024
Drug-induced
acne
is
a
common
side
effect
to
wide
array
of
pharmacological
therapies
and
characterized
by
monomorphic,
papulopustular
eruption
typically
affecting
the
face,
scalp,
upper
thorax.
Corticosteroids
Janus
kinase
inhibitors
(JAKi)
are
commonly
used
for
treatment
inflammatory
bowel
disease
(IBD)
known
aggravate
prior
tendency
or
trigger
development
new
acneiform
eruptions.
Recent
attention
on
managing
drug-induced
has
been
driven
increasing
use
JAKi,
an
expanding
therapeutic
class
in
IBD
several
other
immune-mediated
diseases.
Both
randomized
controlled
trials
real-world
studies
have
identified
as
one
most
treatment-emergent
adverse
events
JAKi.
Left
untreated,
this
skin
reaction
can
significantly
affect
patient
self-esteem
quality
life
leading
poor
adherence
suboptimal
control.
This
review
examines
characteristics
treatments,
provides
practical
guide
gastroenterologists
manage
mild-to-moderate
occurrences,
highlights
when
seek
specialist
dermatology
advice.
Such
approaches
enable
early
often
distressing
event
optimize
management
preventing
premature
discontinuation
dose
reduction
efficacious
drugs.
Язык: Английский