Lung Cancer: Targeted Therapy in 2025
Nicole Bouchard,
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Nathalie Daaboul
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Current Oncology,
Journal Year:
2025,
Volume and Issue:
32(3), P. 146 - 146
Published: March 2, 2025
Lung
cancer
treatment
has
changed
in
the
last
twenty
years
since
discovery
of
EGFR
mutations.
In
this
article,
we
will
review
current
state
art
for
non-small
cell
lung
(NSCLC)
actionable
genomic
alterations
(AGA).
AGAs
are
mostly
found
adenocarcinomas,
a
subtype
cancers.
We
focus
on
mutations,
ALK
fusions,
ROS1
BRAF
V600E
MET
exon
14-skipping
RET
KRAS
G12C
ERBB2
mutations
(also
called
HER2
mutations),
and
NTRK
fusions.
also
touch
key
toxicities
associated
with
these
medications.
Treatments
available
metastatic
stage,
but
discuss
adjuvant
therapy
as
well
stage
III
post-chemoradiotherapy
cancer.
Language: Английский
Real-world pharmacovigilance analysis unveils the toxicity profile of amivantamab targeting EGFR exon 20 insertion mutations in non-small cell lung cancer
BMC Pulmonary Medicine,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: Feb. 6, 2025
While
clinical
trials
have
demonstrated
enduring
responses
to
amivantamab
among
advanced
non-small
cell
lung
cancer
(NSCLC)
patients
bearing
EGFR
exon
20
insertion
mutations,
the
associated
toxicity
profile
in
real-world
scenarios
remains
elusive.
This
pharmacovigilance
study
analyzed
data
from
FDA
Adverse
Event
Reporting
System
(FAERS)
investigate
adverse
events
with
over
period
September
2021
December
2023.
A
comprehensive
disproportionality
analysis
was
performed,
employing
reporting
odds
ratio
(ROR),
proportional
(PRR),
Empirical
Bayes
Geometric
Mean
(EBGM),
and
Bayesian
confidence
propagation
neural
network
calculate
information
components
(ICs),
identify
statistically
significant
events.
proportion
of
(AEs)
attributable
injury,
poisoning,
procedural
complications,
cutaneous
disorders,
respiratory
ailments,
infections,
as
well
vascular
lymphatic
system
disturbances.
There
were
noteworthy
incidences
AEs
including
infusion-related
reactions,
rash,
dyspnea,
pneumonitis,
paronychia,
pulmonary
embolism,
thrombocytopenia,
nausea,
acneiform
dermatitis,
deep
vein
thrombosis,
febrile
neutropenia,
peripheral
edema,
hypokalemia,
neutropenia.
Furthermore,
majority
occurred
within
first
month
following
initiation
treatment,
accounting
for
51.74%
cases.
The
reversibility
amivantamab-related
toxicities
suggests
its
promising
utility
mutations
NSCLC.
Language: Английский
Trends in Overall Survival in Lung Adenocarcinoma with EFGR Mutation, KRAS Mutation, or No Mutation
Martin Faehling,
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Sabine Fallscheer,
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B. Schwenk
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et al.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(7), P. 1237 - 1237
Published: April 5, 2025
Treatment
of
lung
adenocarcinoma
has
changed
and
now
includes
checkpoint
inhibitors
(CPIs)
or,
in
the
case
an
EGFR
mutation,
third-generation
TKI
osimertinib.
Few
data
compare
long-term
overall
survival
(OS)
current
historic
subgroups.
This
real-world
analysis
(KOMPASS
study)
included
stage
IV
lung-adenocarcinoma
patients
with
either
EGFR,
KRAS,
or
no
mutation.
Patients
were
assigned
to
"current"
no-mutation
cohort
if
they
had
mutation
testing
using
NGS
(n
=
199;
median
date
diagnosis
2021).
If
PCR
test
only,
"historic"
127;
2014).
Both
cohorts
significantly
longer
OS
than
respective
(HR
0.58
0.60,
respectively).
The
a
strong
trend
cohorts.
In
cohorts,
improvement
was
due
increase
survivors
0.71),
whereas
improved
without
0.70).
KRAS
showed
like
cohort,
plateau
around
20%.
A
comparison
our
that
phase
III
trials
KEYNOTE-189
FLAURA
suggests
outcomes
are
use
CPIs
clinical
trial
results
well
translated
into
practice
comparable
OS.
benefit
from
CPI
treatment
patients.
Language: Английский