Efficacy and safety of antiviral plus anti-spike monoclonal antibody combination therapy vs. monotherapy for high-risk immunocompromised patients with mild-to-moderate SARS-CoV2 infection during the Omicron era: A prospective cohort study
International Journal of Antimicrobial Agents,
Journal Year:
2024,
Volume and Issue:
63(3), P. 107095 - 107095
Published: Jan. 21, 2024
Antivirals
and
monoclonal
antibodies
are
available
to
lower
progression
risk
in
immunocompromised
patients.
However,
combination
therapy
with
both
types
of
agents
has
not
been
studied.
Single-centre
prospective
cohort
study.
We
enrolled
all
patients
who
received
treatment
for
mild-to-moderate
COVID-19
from
January
1st,
2022,
October
30th,
2022.
Primary
endpoint
was
at
90
days,
defined
as
hospital
admission
or
death
due
and/or
seronegative
persistent
Three
hundred
four
(304)
were
included.
43
(14.1%)
sotrovimab
plus
a
direct-acting
antiviral
261
(85.9%)
monotherapy.
outcome
occurred
more
frequently
after
monotherapy
(4.6%
vs
0%,
p=0.154).
Among
anti-Spike
IgG
titter
below
750
BAU/mL,
frequent
(23.9%
p=0.001),
including
COVID-related
(15.2%
p=0.014)
(10.9%
p=0.044).
Combination
associated
(OR
0.08,
95%
CI
0.01-0.64).
Anti-S
than
BAU/mL
previous
antiCD20
higher
13.70,
2.77-67.68;
OR
3.05,
1.20-10.94,
respectively).
In
immunocompromised,
an
may
be
effective
SARS-CoV2.
Language: Английский
Monoclonal antibodies as COVID-19 prophylaxis therapy in immunocompromised patient populations
International Journal of Infectious Diseases,
Journal Year:
2023,
Volume and Issue:
134, P. 228 - 238
Published: July 1, 2023
The
objective
of
this
review
was
to
examine
the
latest
literature
regarding
effectiveness
monoclonal
antibodies
as
COVID-19
prophylaxis
therapy
for
immunocompromised
patient
populations.Literature
published
real-world
and
randomized
control
trials
(RCTs)
from
2020
May
2023.COVID-19
is
highly
transmissible
with
potentially
serious
health
outcomes,
underscoring
need
effective
prevention
treatment
strategies.
Vaccines
are
at
preventing
general
population;
however,
efficacy
often
impaired
in
patients
given
insufficient
response
initial
exposure
and/or
memory
secondary
exposures.
Some
individuals
may
also
have
contraindications
vaccination.
As
such,
additional
protective
measures
needed
bolster
immune
these
populations.
Monoclonal
been
bolstering
system
responses
among
patients;
they
proving
ineffective
against
most
recent
Omicron
strains
(BA.4
BA.5).Several
studies
investigated
pre-
post-prophylaxis
COVID-19.
Historical
evidence
promising;
new
variants
concern
challenging
currently
available
regimens.
Language: Английский
Real-World Effectiveness of Sotrovimab for the Early Treatment of COVID-19: Evidence from the US National COVID Cohort Collaborative (N3C)
Clinical Drug Investigation,
Journal Year:
2024,
Volume and Issue:
44(3), P. 183 - 198
Published: Feb. 20, 2024
The
coronavirus
disease
2019
(COVID-19)
pandemic
has
been
an
unprecedented
healthcare
crisis,
one
that
threatened
to
overwhelm
health
systems
and
prompted
urgent
need
for
early
treatment
options
patients
with
mild-to-moderate
COVID-19
at
high
risk
progression
severe
disease.
Randomised
clinical
trials
established
the
safety
efficacy
of
monoclonal
antibodies
(mAbs)
in
pandemic;
vitro
data
subsequently
led
use
mAbs
being
discontinued,
without
clear
evidence
on
how
these
were
linked
outcomes.
In
this
study,
we
describe
compare
real-world
outcomes
treated
sotrovimab
versus
untreated
patients.
Language: Английский
Resistance Analysis Following Sotrovimab Treatment in Participants with COVID-19 During the Phase III COMET-ICE Study
Sambhavi Subramanian,
No information about this author
Gretja Schnell,
No information about this author
Julia di Iulio
No information about this author
et al.
Future Virology,
Journal Year:
2023,
Volume and Issue:
18(15), P. 975 - 990
Published: Oct. 1, 2023
Aim:
Sotrovimab
is
an
engineered
human
monoclonal
antibody
that
binds
a
conserved
region
of
the
SARS-CoV-2
spike
protein.
The
COMET-ICE
phase
III
study
evaluated
sotrovimab
for
treatment
mild
to
moderate
COVID-19
in
nonhospitalized
participants
with
≥1
risk
factor
severe
disease
progression.
Materials
&
methods:
We
presence
circulating
variants
concern
or
interest
(VOCs/VOIs)
and
characterized
baseline,
post-baseline
emergent
amino
acid
substitutions
detected
epitope
SARS-CoV-2.
Results:
None
sotrovimab-treated
baseline
substitutions,
1
48
met
primary
clinical
endpoint
Conclusion:
Overall,
progression
was
not
associated
identified
VOC/VOI
participants.
Language: Английский
Sotrovimab in Severe COVID-19 anti-S Seronegative Immunocompromised Patients: Multicenter Retrospective Cohort
Rubén Lobato-Cano,
No information about this author
Alberto Romero-Palacios,
No information about this author
Laurine Prinet
No information about this author
et al.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 6, 2024
Abstract
Purpose:
Sotrovimab’s
effectiveness
remains
uncertain
in
severely
immunocompromised
inpatients
with
COVID-19,
particularly
amidst
the
emergence
of
Omicron
subvariants.
Our
study
aimed
to
evaluate
clinical
progress
and
safety
severe
COVID-19
at-risk
treated
sotrovimab.
Methods:
Retrospective
multicentric
cohort
(four
teaching
hospitals
from
Andalusian
Health
System)
that
included
adult
inmunosupression
negative
anti-S
serology
who
received
sotrovimab
December
2021
March
2023.
Primary
outcomes
focused
on
respiratory
progression
(High-flow
oxygen/Invasive
Non-invasive
support
mortality
at
28-day)
while
secondary
variables
encompassed
hospital
stay
duration
readmission
reasons.
Results:
79
patients
were
included,
58.2%
male,
a
median
age
72
years
(P
25-P
75
65-79).
Significant
immunosuppression
factors
hematologic
neoplasms
51.9%
patients,
solid
organ
transplants
17.7%,
13.9%
systemic
autoimmune
diseases.
The
interval
between
symptom
onset
infusion
was
12
days
(P
25-P
75
8-22),
13
13-26).
36.7%
deceased,
32.9%
attributed
directly
COVID-19.
No
adverse
reactions
reported.
Univariate
analysis
linked
severity
admission
(p<0.05).
Patients
distributed
among
dominant
subvariants
across
five
periods:
BA.1
(15%),
BA.2
(25%),
BA.3
(31.3%),
BQ.1
(16.3%),
XBB.1.5
(11.4%).
Conclusions
The
underscores
need
for
further
investigations
establish
sotrovimab's
efficacy
cases
immunocompromise.
Early
treatment
initiation
may
be
crucial
considering
potential
limitations
its
use
advanced
forms.
Language: Английский
Clinical practice guideline supported administration of monoclonal antibody therapy for high-risk patients with COVID-19: Experience of a quaternary care centre
Keely Hammond,
No information about this author
François Bourdeau,
No information about this author
Marina Klein
No information about this author
et al.
Journal of the Association of Medical Microbiology and Infectious Disease Canada,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 3, 2024
Background:
Immunocompromised
patients
remain
at
risk
of
progression
to
severe
COVID-19
disease.
Methods:
We
describe
clinical
COVID-19-related
outcomes
after
administration
anti-SARS-CoV-2
monoclonal
antibodies
(mAb)
following
institutional
practice
guidelines
(CPGs)
in
205
high-risk
between
November
2021
and
April
2022
a
Canadian
quaternary
care
centre.
Results:
Median
patient
age
was
59
years;
102
(50%)
were
female.
Eighty-two
(40%)
transplant
recipients,
47
(23%)
had
hematologic
malignancies,
25
(12%)
solid
organ
51
(25%)
another
indication.
Forty-eight
received
fewer
than
two
doses
vaccines.
The
majority
(80%)
mild
disease
presentation
with
14%
moderate
6%
severe.
time
from
symptom
onset
mAb
3
days
(IQR
2.0-5.5
days).
Of
those
who
as
outpatients,
90
(93%)
favourable
(no
hospitalizations
or
death
within
months).
inpatients,
93
(86%)
(discharged
without
re-admission
death),
4%
re-admitted,
10%
died.
In
logistic
regression
analysis,
only
severity
associated
unfavourable
outcomes.
Fewer
vaccine
not
outcomes,
suggesting
potential
benefit
among
the
under-vaccinated.
There
significant
difference
adherence
CPGs
outpatients
versus
inpatients
(adherent
for
85%
58%,
p<0.001),
where
non-adherence
occurred
cases
Conclusion:
CPG-supported
management
may
be
useful
model
guide
future
therapies.
Language: Английский
Host-Directed Adjunctive Therapies in Immunocompromised Patients with Pneumonia
Clinics in Chest Medicine,
Journal Year:
2024,
Volume and Issue:
46(1), P. 37 - 48
Published: Dec. 9, 2024
Language: Английский
Clinical experience in the treatment of COVID-19 with monoclonal antibodies in solid organ transplant recipients
Elena Múñez,
No information about this author
Jorge Calderón‐Parra,
No information about this author
Andrea Gutiérrez‐Villanueva
No information about this author
et al.
Revista Española de Quimioterapia,
Journal Year:
2023,
Volume and Issue:
36(Suppl1), P. 25 - 28
Published: Nov. 24, 2023
Solid
organ
transplant
(SOT)
recipients
are
at
high
risk
for
complications
from
coronavirus
disease
2019
(COVID-19).
SOT
mount
lower
immunological
responses
to
vaccines
than
general
population
and
breakthrough
COVID-19
infections.
Passive
immunotherapy
in
the
form
of
anti-Spike
monoclonal
antibodies
(MoAbs)
may
be
an
alternative
prophylaxis
treatment
these
patients.
SARS-CoV-2
has
evolved
by
accumulating
resistance
mutations
that
have
escaped
neutralizing
action
most
MoAbs.
However,
MoAbs
directed
more
conserved
epitopes
maintain
effector
functions
could
efficacy
According
published
data,
with
low
anti-spike
antibody
vaccination
benefit
use
pre-exposure
prophylaxis,
mild
moderate
severe
less
15
days
symptom
duration
oxygen
requirements.
Combination
therapy
effective
monotherapy
mild-to-moderate
infection.
Language: Английский