Breast Cancer Research and Treatment,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 12, 2025
To
evaluate
the
prognostic
significance
of
changes
in
pre-
and
post-neoadjuvant
chemotherapy
(NACT)
Ki67
patients
with
primary
invasive
triple-negative
breast
cancer
(TNBC).
Population-based
registry
data
were
retrieved
for
diagnosed
TNBC
between
2007
2021
(n
=
9262).
Multivariable
Cox
regression
analysis
was
performed
disease-specific
survival
(DSS)
overall
(OS)
adjusted
age
residual
disease
nodes
(RDBN).
Of
1777
receiving
NACT,
54
achieved
pathologic
complete
response
(pCR)
755
had
disease.
Most
overweight
stage
II
(78%),
grade
3
tumors
(53%),
RDBN
score
(42%).
Compared
to
baseline,
tumor
size
(30
vs.
15
mm;
P
<
0.0001)
levels
(63%
48%;
2.2e
-
16)
generally
decreased
after
NACT.
Although
only
5%
samples
increased
size,
often
remained
unchanged
(75%)
or
(0.9%)
treatment,
respectively.
However,
34%
discontinued
treatment.
Patients
showing
no
Ki67%
more
unfavorable
OS
(P
DSS
0.00032),
significantly
lower
5-year
probabilities
(OS:
66%;
DSS:
78%)
than
those
87%;
89%).
All
reaching
pCR
alive
5
years
diagnosis.
an
independent
predictor
multivariable
analyses.
treated
neoadjuvant
chemotherapy,
resulting
adverse
clinical
outcomes.
These
findings
highlight
need
individualized
treatment
regimens
dynamic
monitoring
high
post-NACT.
JAMA Oncology,
Journal Year:
2023,
Volume and Issue:
9(11), P. 1557 - 1557
Published: Sept. 21, 2023
Sentinel
lymph
node
biopsy
(SLNB)
is
the
standard
of
care
for
axillary
staging
patients
with
early
breast
cancer
(BC),
but
its
necessity
can
be
questioned
since
surgery
examination
nodes
not
performed
curative
intent.
Cancer Treatment Reviews,
Journal Year:
2022,
Volume and Issue:
105, P. 102375 - 102375
Published: March 4, 2022
Adjuvant
and
neoadjuvant
breast
cancer
treatments
can
reduce
mortality
but
may
increase
from
other
causes.
Information
regarding
treatment
benefits
risks
is
scattered
widely
through
the
literature.
To
inform
clinical
practice
we
collated
reviewed
highest
quality
evidence.Guidelines
were
searched
to
identify
adjuvant
or
options
recommended
in
early
invasive
cancer.
For
each
option,
systematic
literature
searches
identified
highest-ranking
evidence.
radiotherapy
risks,
for
dose-response
relationships
modern
organ
doses
also
undertaken.Treatment
USA
elsewhere
included
chemotherapy
(anthracycline,
taxane,
platinum,
capecitabine),
anti-human
epidermal
growth
factor
2
therapy
(trastuzumab,
pertuzumab,
trastuzumab
emtansine,
neratinib),
endocrine
(tamoxifen,
aromatase
inhibitor,
ovarian
ablation/suppression)
bisphosphonates.
Radiotherapy
after
conserving
surgery
(whole
breast,
partial
tumour
bed
boost,
regional
nodes)
mastectomy
(chest
wall,
nodes).
Treatment
supported
by
randomised
evidence,
including
>
10,000
women
eight
comparisons,
1,000-10,000
fifteen
<
1,000
one.
Most
comparisons
reduced
recurrence
10-25%,
with
no
non-breast-cancer
death.
Anthracycline
increased
overall
mortality.
risk
was
heart
disease
leukaemia.
Radiation-risks
mainly
disease,
lung
oesophageal
cancer,
increasing
heart,
oesophagus
radiation
respectively.
Taxanes
leukaemia
risk.These
decisions
individuals
recommendations
groups
of
women.
Cancer Communications,
Journal Year:
2022,
Volume and Issue:
42(10), P. 913 - 936
Published: Sept. 8, 2022
Breast
cancer
is
the
most
common
worldwide.
The
occurrence
of
breast
associated
with
many
risk
factors,
including
genetic
and
hereditary
predisposition.
cancers
are
highly
heterogeneous.
Treatment
strategies
for
vary
by
molecular
features,
activation
human
epidermal
growth
factor
receptor
2
(HER2),
hormonal
receptors
(estrogen
[ER]
progesterone
[PR]),
gene
mutations
(e.g.,
1/2
[BRCA1/2]
phosphatidylinositol-4,5-bisphosphate
3-kinase
catalytic
subunit
alpha
[PIK3CA])
markers
immune
microenvironment
tumor-infiltrating
lymphocyte
[TIL]
programmed
death-ligand
1
[PD-L1]).
Early-stage
considered
curable,
which
local-regional
therapies
(surgery
radiotherapy)
cornerstone,
systemic
therapy
given
before
or
after
surgery
when
necessary.
Preoperative
neoadjuvant
therapy,
targeted
drugs
checkpoint
inhibitors,
has
become
standard
care
early-stage
HER2-positive
triple-negative
cancer,
followed
risk-adapted
post-surgical
strategies.
For
ER-positive
early
endocrine
5-10
years
essential.
Advanced
distant
metastases
currently
incurable.
Systemic
in
this
setting
include
agents,
such
as
CDK4/6
inhibitors
phosphoinositide
(PI3K)
hormone
receptor-positive
disease,
anti-HER2
poly(ADP-ribose)
polymerase
BRCA1/2
mutation
carriers
immunotherapy
part
disease.
Innovation
technologies
precision
medicine
may
guide
individualized
treatment
escalation
de-escalation
future.
In
review,
we
summarized
latest
scientific
information
discussed
future
perspectives
on
cancer.
Journal of Clinical Oncology,
Journal Year:
2021,
Volume and Issue:
40(3), P. 282 - 293
Published: Dec. 7, 2021
Palbociclib
is
a
cyclin-dependent
kinase
4
and
6
inhibitor
approved
for
advanced
breast
cancer.
In
the
adjuvant
setting,
potential
value
of
adding
palbociclib
to
endocrine
therapy
hormone
receptor-positive
cancer
has
not
been
confirmed.
Annals of Oncology,
Journal Year:
2023,
Volume and Issue:
34(11), P. 970 - 986
Published: Sept. 6, 2023
The
18th
St
Gallen
International
Breast
Cancer
Conference
held
in
March
2023,
Vienna,
Austria,
assessed
significant
new
findings
for
local
and
systemic
therapies
early
breast
cancer
with
a
focus
on
the
evaluation
of
multimodal
treatment
options.
emergence
more
effective,
innovative
agents
both
preoperative
(primary
or
neoadjuvant)
post-operative
(adjuvant)
settings
has
underscored
pivotal
role
multidisciplinary
approach
decision
making,
particularly
when
selecting
therapy
an
individual
patient.
importance
discussions
regarding
clinical
benefits
interventions
was
explicitly
emphasized
by
consensus
panel
as
integral
part
developing
optimal
plan
'right'
degree
intensity
duration.
panelists
focused
controversies
surrounding
management
common
ductal/no
special
type
lobular
histology,
which
account
vast
majority
tumors.
expert
opinion
based
interpretations
available
data,
well
current
practices
their
professional
environments,
personal
socioeconomic
factors
affecting
patients,
cognizant
varying
reimbursement
accessibility
constraints
around
world.
strongly
advocated
patient
participation
well-designed
studies
whenever
feasible.
With
these
considerations
mind,
Consensus
aims
to
offer
guidance
clinicians
appropriate
treatments
early-stage
assist
balancing
realistic
trade-offs
between
benefit
toxicity,
enabling
patients
make
well-informed
choices
through
shared
decision-making
process.
npj Breast Cancer,
Journal Year:
2022,
Volume and Issue:
8(1)
Published: May 20, 2022
Approximately
a
half
of
breast
tumors
classified
as
HER2-negative
exhibit
HER2-low-positive
expression.
We
recently
described
high
instability
expression
from
primary
cancer
(BC)
to
relapse.
Previous
studies
reporting
discordance
in
HER2
status
between
baseline
biopsy
and
residual
disease
(RD)
patients
undergoing
neoadjuvant
treatment
did
not
include
the
category.
The
aim
this
study
is
track
evolution
BC
RD
after
treatment.
Patients
with
available
tumor
tissue
matched
samples
(in
case
no
pCR)
were
included.
cases
sub-classified
HER2-0
or
(IHC
1+
2+
ISH
negative).
Four-hundred
forty-six
Primary
phenotype
was:
HR-positive/HER2-negative
23.5%,
triple-negative
(TN)
35%,
HER2-positive
41.5%.
55.6%
cohort
significantly
enriched
vs.
TN
subgroup
(68.6%
46.8%,
p
=
0.001
χ2
test).
In
all,
35.3%
non-pCR
(n
291)
had
on
RD.
overall
rate
was
26.4%,
mostly
driven
by
converting
either
(14.8%)
(8.9%)
phenotype.
Among
RD,
32.0%
57.1%
an
estimated
risk
relapse
according
proliferative
burden
CPS-EG
score,
respectively.
conclusion,
showed
may
guide
personalized
adjuvant
for
high-risk
context
clinical
trials
novel
anti-HER2
antibody-drug
conjugates.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: March 1, 2023
Our
previous
studies
have
showed
that
C-C
motif
chemokine
ligand
20
(CCL20)
advanced
tumor
progression
and
enhanced
the
chemoresistance
of
cancer
cells
by
positively
regulating
breast
stem
cell
(BCSC)
self-renewal.
However,
it
is
unclear
whether
CCL20
affects
remodeling
microenvironment
(TME).
Here,
we
observed
polymorphonuclear
myeloid-derived
suppressor
(PMN-MDSCs)
were
remarkably
enriched
in
TME
CCL20-overexpressing
orthotopic
allograft
tumors.
Mechanistically,
activated
differentiation
granulocyte-monocyte
progenitors
(GMPs)
via
its
receptor
6
(CCR6)
leading
to
PMN-MDSC
expansion.
PMN-MDSCs
from
tumors
(CCL20-modulated
PMN-MDSCs)
secreted
amounts
C-X-C
2
(CXCL2)
increased
ALDH+
BCSCs
activating
CXCR2/NOTCH1/HEY1
signaling
pathway.
Furthermore,
(CXCR2)
antagonist
SB225002
docetaxel
(DTX)
effects
on
growth
decreasing
CCL20high-expressing
These
findings
elucidated
how
modulated
promote
development,
indicating
a
new
therapeutic
strategy
interfering
with
interaction
between
cancer,
especially
cancer.