Juan Cuevas eBooks,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 1, 2024
La
medicina
interna
desempeña
un
papel
fundamental
en
la
atención
primaria
de
salud,
siendo
base
para
el
manejo
integral
una
amplia
variedad
enfermedades.
En
este
contexto,
libro
"Guía
Esencial
Medicina
Interna
Primer
Nivel
Atención
Tomo
14"
se
presenta
como
herramienta
invaluable
los
profesionales
salud
que
trabajan
primer
nivel
atención,
ofreciendo
orientación
clara
y
concisa
sobre
las
condiciones
médicas
más
comunes.
The Lancet Regional Health - Europe,
Journal Year:
2024,
Volume and Issue:
38, P. 100838 - 100838
Published: March 1, 2024
In
the
past
two
decades,
treatment
of
metastatic
non-small
cell
lung
cancer
(NSCLC),
has
undergone
significant
changes
due
to
introduction
targeted
therapies
and
immunotherapy.
These
advancements
have
led
need
for
predictive
molecular
tests
identify
patients
eligible
therapy.
This
review
provides
an
overview
development
current
application
biomarker
testing
in
European
with
advanced
stage
NSCLC.
Using
data
from
eleven
countries,
we
conclude
that
recommendations
are
incorporated
national
guidelines
across
Europe,
although
there
differences
their
comprehensiveness.
Moreover,
availability
recently
EMA-approved
varies
between
countries.
Unfortunately,
routine
assessment
national/regional
rates
is
limited.
As
a
result,
it
remains
uncertain
which
proportion
NSCLC
Europe
receive
adequate
testing.
Lastly,
Molecular
Tumor
Boards
(MTBs)
discussion
test
results
widely
implemented,
but
composition
functioning
lacking.
The
establishment
MTB
can
provide
framework
interpreting
rare
or
complex
mutations,
facilitating
appropriate
decision-making,
ensuring
quality
control.
Histopathology,
Journal Year:
2024,
Volume and Issue:
85(1), P. 3 - 19
Published: March 5, 2024
The
significant
clinical
benefits
of
human
epidermal
growth
factor
receptor
2
(HER2)‐targeted
therapeutic
agents
have
revolutionized
the
treatment
landscape
in
a
variety
solid
tumours.
Accordingly,
accurate
evaluation
HER2
status
these
different
tumour
types
is
critical
for
decision
making
to
select
appropriate
patients
who
may
benefit
from
life‐saving
HER2‐targeted
therapies.
biomarker
scoring
criteria
organ
systems,
and
close
adherence
corresponding
testing
guidelines
their
updates,
if
available,
essential
evaluation.
In
addition,
knowing
unusual
patterns
expression
also
important
avoid
inaccurate
this
review,
we
discuss
key
considerations
when
evaluating
tumours
making,
including
tissue
handling
preparation
testing,
as
well
pathologist's
readout
results
breast
carcinomas,
gastroesophageal
adenocarcinomas,
colorectal
gynaecologic
non‐small
cell
lung
carcinomas.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(6), P. 1705 - 1705
Published: March 10, 2023
Next-generation
sequencing
(NGS)
is
a
molecular
approach
able
to
provide
comprehensive
profile
of
non-small
cell
lung
cancer
(NSCLC).
The
broad
spectrum
biomarker-guided
therapies
has
positioned
diagnostic
laboratories
as
central
component
patient
clinical
management.
Here,
we
show
the
results
an
UNE-EN
ISO
15189:2022
NGS-accredited
assay
in
cohort
350
patients.
TP53
(51.0%),
KRAS
(26.6%)
and
EGFR
(12.9%)
were
most
frequently
mutated
genes.
Furthermore,
detected
co-occurring
mutually
exclusive
alterations,
well
distinct
profiles
according
sex
smoking
habits.
Actionable
genetic
alterations
significantly
more
frequent
female
patients
(80.5%,
p
<
0.001)
never-smoker
(87.7%,
0.001).
When
NGS
was
established
main
testing
strategy,
36.4%
received
at
least
one
line
targeted
treatment.
Among
200
with
stage
IV
NSCLC,
first-line
treatment
associated
longer
progression-free
survival
(PFS)
(13.4
months
(95%
CI,
10.2-16.6)
(p
=
0.001)).
Similarly,
overall
(OS)
receiving
drug
(26.2
11.8-40.5)
Our
that
implementation
public
healthcare
system
provided
broader
application
precision
medicine.
Revista Española de Patología,
Journal Year:
2025,
Volume and Issue:
58(1), P. 100799 - 100799
Published: Jan. 1, 2025
Microscopic
assessment
is
essential
in
the
study
of
mediastinal
lymph
nodes.
Obtaining
cytological
samples
through
Endobronchial
Ultrasound
TransBronchial
Needle
Aspiration
(EBUS-TBNA)
has
long
been
considered
gold
standard
procedure.
The
implementation
World
Health
Organization
(WHO)
Reporting
System
for
Lymph
Node
Cytopathology,
along
with
advancement
CryoEBUS
node
technique,
enhanced
and
refined
diagnostic
accuracy
this
field.
During
a
two-year
period,
cases
involving
parallel
performance
EBUS-TBNA
specimen
collection
were
quantified.
WHO
allowed
comparison
yield
between
tissue
samples.
A
total
178
procedures
conducted,
mean
patient
age
63
years
male
predominance
72.5%.
station
7
was
most
sampled
site,
accounting
38.76%
cases.
Category
V
-
malignant
common
diagnosis,
representing
50%
cases,
while
46.62%
malignant.
Pearson
correlation
coefficient
two
methods
calculated
at
0.99.
combined
Cytopathology
simultaneous
use
resulted
accuracy,
reducing
non-diagnostic
to
less
than
3%.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(5), P. 744 - 744
Published: Feb. 22, 2025
Objectives:
The
purpose
of
this
study
is
to
assess
the
clinical
impact
next-generation
sequencing
(NGS),
as
an
increasingly
available
and
advantageous
tool,
for
glioblastoma
patients.
Methods:
Adult
patients
aged
less
than
65,
surgically
treated
between
2010-2021,
were
included.
Tumor
samples
analyzed
with
NGS
using
Oncomine
Comprehensive
v3
(OCA)
panel
Ion
Reporter
Genexus
v5.9.1
(Thermo
Fisher
Scientific).
Results:
Thirty-two
included,
a
median
age
47.7
years
overall
survival
25
months.
Identification
mutations
by
resulted
in
change
diagnosis
two
cases.
In
all
but
one,
at
least
one
genetic
alteration
was
detected
(median
three
per
patient),
most
commonly
EGFR
amplification.
93.7%
patients,
biomarkers
that
make
them
potentially
eligible
trial
found.
No
differences
seen
regarding
alterations,
although
trend
towards
better
those
without
CDK4
mutation
observed
(p
=
0.088).
Conclusions:
use
provides
useful
information
diagnosis,
especially
young
it
will
probably
become
valuable
decision-making
more
therapeutic
targets
treatments
emerge.
For
moment,
crucial
scientific
progress
happen.
Revista Española de Patología,
Journal Year:
2025,
Volume and Issue:
58(3), P. 100824 - 100824
Published: April 17, 2025
Non-small
cell
lung
cancer
(NSCLC)
can
arise
from
insertions
in
exon
20
of
the
EGFR
gene,
among
other
alterations.
We
carried
out
an
external
quality
assessment
(EQA)
to
evaluate
accuracy
laboratory
methods
and
highlight
importance
detecting
identifying
genetic
alterations,
such
as
insertion,
patients
with
NSCLC.
The
2021
EGRF
EQA
program
consisted
two
rounds,
which
four
formalin-fixed
paraffin-embedded
specimens
(round
1:
positive
for
insertions/duplications,
one
a
common
alteration,
wild-type;
round
2:
three
insertions/duplications
wild-type)
obtained
NSCLC
were
tested.
Approximately
80%
invited
laboratories
participated
each
round.
most
DNA
isolation
techniques
used
cobas®
Sample
Preparation
Kit
(46.7%)
1
QIAamp
(37.1%)
2.
frequently
genotyping
method
both
rounds
was
Mutation
Test
53.3%;
37.1%).
In
71.1%
73.6%
tests,
respectively,
reported
expected
result.
lowest
success
rate
observed
H773delinsRY
Exon
determination
17.8%;
31.4%).
This
alteration
correctly
determined
only
by
next-generation
sequencing.
variability
our
study
Spain
ensure
high
performance.
Diagnostics,
Journal Year:
2025,
Volume and Issue:
15(9), P. 1064 - 1064
Published: April 22, 2025
Background/Objectives:
Recent
advances
in
the
treatment
of
non-small
cell
lung
cancer
(NSCLC)
have
shifted
from
conventional
chemotherapy
to
targeted
therapies
aimed
at
specific
genetic
mutations,
particularly
adenocarcinoma
subtype.
These
improved
overall
survival
and
quality
life.
However,
some
patients
still
face
barriers
accessing
these
treatments
due
challenges
diagnosing
advanced-stage
NSCLC.
Limited
tumor
cellularity
small
biopsies
cytological
samples
hinders
ability
perform
further
molecular
analyses.
Additionally,
increasing
number
alterations
requiring
testing
complicates
diagnostic
process.
To
overcome
this
challenge,
we
propose
combining
endobronchial
ultrasound-guided
transbronchial
needle
aspiration
(EBUS-TBNA)
with
next-generation
sequencing
(NGS)
immunohistochemistry
for
PD-L1.
Methods:
A
total
120
EBUS-TBNA
were
consecutively
collected
during
first
year
integrating
NGS
a
reference
hospital
Castilla
y
León,
Spain.
Depending
on
histology
patient
characteristics,
67
analyses
116
PD-L1
determinations
performed.
Results:
The
sample
obtained
cases
successfully
achieved
triple
objective
proposed
by
NCCN
(diagnosis,
staging,
analysis
single
procedure)
97%
instances.
Conclusions:
Our
study
highlights
effectiveness
as
comprehensive,
cost-effective,
safe
tool
NSCLC,
achieving
diagnosis,
cases.
procedure
consistently
provided
high-quality
testing,
minimal
complications,
reinforcing
its
value
reliable
approach
optimizing
personalized
strategies.