Outcomes of COVID‐19 in patients with lymphomas participating in registered clinical trials: A real‐world study from China in the Omicron outbreak era
Peng Sun,
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Hang Yang,
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Baitian Zhao
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et al.
Cancer Medicine,
Journal Year:
2023,
Volume and Issue:
12(23), P. 21148 - 21158
Published: Nov. 27, 2023
Abstract
Background
This
real‐world
study
investigated
the
outcome
of
COVID‐19
in
lymphoma
patients
participating
registered
clinical
trials
and
explored
potential
risk
factors
with
during
first
wave
Omicron
outbreak
China.
Methods
One
hundred
ten
diagnosed
our
center
between
December
1,
2022,
January
31,
2023,
were
included.
Results
Four
(3.6%)
identified
as
severe
2
(1.8%)
critical
COVID‐19,
respectively.
The
mortality
rate
observed
was
2.73%
for
entire
cohort,
33.3%
severe/critical
group,
18.8%
hospitalized
group.
90‐day
OS
98.2%
66.7%
87.5%
Advanced
age
(≥70
years),
comorbidities,
PI3K
inhibitor‐containing
regimen
significantly
associated
severity
COVID‐19.
Patients
indolent
B‐cell
non‐Hodgkin
lymphomas
less
likely
to
be
Conclusion
reported
similar
features
cohort
that
non‐hematological
malignancy
(HM)
patients,
while
proportion
relatively
higher
than
non‐HM
patients.
Our
findings
provided
valuable
experience
aid
researchers
managing
ongoing
pandemic
variant.
Language: Английский
Long-Term Immunological Alertness and Response to COVID-19 Vaccination—Conditions for Prevention in Early Palliative Oncological Care Patients
Peter Priester,
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Miroslav Fajfr,
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Veronika Molnárová
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et al.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(3), P. 299 - 299
Published: March 13, 2024
Aside
from
the
general
population,
COVID-19
pandemic
has
also
affected
a
group
of
patients
in
palliative
oncology
care.
In
this
study,
long-term
immune
responses
against
SARS-CoV-2
after
vaccination
were
monitored
cohort
This
non-randomized,
prospective,
and
open-label
pilot
study
recruited
Palliative
Oncology
Program
included
147
patients,
which
80
females
(54.4%)
67
males
(45.6%).
The
overall
evaluation
current
health
status,
anti-S
IgG
titer,
neutralizing
antibodies
using
virus
neutralization
test
(VNT).
Anti-S
antibody
analysis
revealed
high
(H)
levels
35.7%
(n
=
10)
very
(VH)
39.3%
11)
second
dose.
Similarly,
third
dose,
H
was
found
29.6%
32)
VH
55.5%
60)
patients.
High
consistent
with
VNT
titers
(>2560)
17.1%
12)
or
82.9%
58)
Patients
two
more
doses
showed
at
median
451
342
days
vaccination,
respectively.
clinical
trial,
over
longer
period
time.
These
did
not
show
reduced
immunological
to
vaccine
challenge.
We
can
assume
that
prevention
through
reduce
risk
complications
death
early
Language: Английский