Current Oncology,
Год журнала:
2023,
Номер
31(1), С. 145 - 167
Опубликована: Дек. 26, 2023
The
prevalence
of
breast
cancer
amongst
older
adults
in
Canada
is
increasing.
This
patient
population
faces
unique
challenges
the
management
cancer,
as
often
have
distinct
biological,
psychosocial,
and
treatment-related
considerations.
paper
presents
an
expert
consensus
Canadian
treatment
landscape,
focusing
on
key
considerations
for
optimizing
selection
systemic
therapy
advanced
adults.
aims
to
provide
evidence-based
recommendations
practical
guidance
healthcare
professionals
involved
care
with
cancer.
By
recognizing
addressing
specific
needs
adults,
providers
can
optimize
outcomes
improve
overall
quality
this
population.
ESMO Open,
Год журнала:
2025,
Номер
10(1), С. 104103 - 104103
Опубликована: Янв. 1, 2025
Randomized
controlled
trials
have
shown
inconsistent
overall
survival
(OS)
benefit
among
the
three
cyclin-dependent
kinase
4/6
inhibitors
(CDK4/6i)
as
first-line
(1L)
treatment
of
patients
with
hormone
receptor-positive
(HR+)/human
epidermal
growth
factor
receptor
2-negative
(HER2-)
metastatic
breast
cancer
(mBC).
Several
real-world
studies
compared
CDK4/6i
effectiveness,
findings.
This
study
HR+/HER2-
mBC
receiving
1L
palbociclib,
ribociclib,
or
abemaciclib,
in
combination
an
aromatase
inhibitor
(AI),
US
clinical
practice.
Targeted Oncology,
Год журнала:
2024,
Номер
19(3), С. 303 - 320
Опубликована: Март 28, 2024
Palbociclib
in
combination
with
endocrine
therapy
is
approved
for
treatment
of
hormone
receptor-positive
(HR+)/human
epidermal
growth
factor
receptor
2-negative
(HER2−)
advanced
breast
cancer.
In
addition
to
clinical
trials,
several
real-world
studies
have
evaluated
the
effectiveness
palbociclib.
With
increased
life
expectancy
general
population,
cancer
older
women
also
expected
increase.
The
aim
was
systematically
review
evidence
from
both
trials
and
palbociclib
outcomes
patients
HR+/HER2−
advanced/metastatic
(a/mBC).
Older
are
often
underrepresented
(RWE)
will
enrich
analysis
this
subgroup
patients.
A
systematic
literature
search
PubMed,
EMBASE,
Cochrane
Library
through
May
4,
2023,
yielded
2355
unique
articles.
total
52
articles
(13
39
reporting
results
seven
randomized
controlled
[RCTs]
37
RWE
studies,
respectively)
were
included
based
on
study
eligibility
criteria.
All
RCTs
used
age
cutoffs
≥
65
years
define
population
(n
=
722;
437
received
palbociclib);
all
except
one
an
cutoff
>
60
years,
had
or
higher
9840;
7408
palbociclib).
Overall,
that
compared
efficacy
(progression-free
survival
[seven
RCTs,
20
studies],
overall
[four
11
tumor
response
[three
benefit
rate
[one
RCT,
two
studies])
safety
(three
three
studies)
between
younger
patients,
showed
similar
benefits,
regardless
age.
Results
global
quality
(QoL)
maintained
receiving
dose
modifications
(two
studies),
reductions
(one
discontinuation
rates
patients;
however,
these
differences
did
not
appear
adversely
impact
outcomes.
review,
data
effective,
well
tolerated,
QoL
a/mBC.
settings
associated
as
RCTs.
CRD42023444195.
Frontiers in Oncology,
Год журнала:
2023,
Номер
13
Опубликована: Сен. 28, 2023
Elderly
patients
are
generally
underrepresented
in
oncology
clinical
trials;
therefore,
real-world
data
needed
to
inform
management
of
elderly
with
hormone
receptor-positive/human
epidermal
growth
factor
receptor
2-negative
(HR+/HER2-)
metastatic
breast
cancer
(mBC).
This
subanalysis
the
P-REALITY
X
study
(NCT05361655)
evaluated
palbociclib
treatment
patterns
and
comparative
effectiveness
plus
an
aromatase
inhibitor
(AI)
versus
AI
alone
among
HR+/HER2-
mBC
aged
≥
75
years
treated
routine
practice
United
States.This
retrospective
observational
cohort
used
electronic
health
records
from
Flatiron
Health
Analytic
Database.
Palbociclib
patterns,
overall
survival
(OS),
progression-free
(rwPFS),
time
chemotherapy
(TTC)
were
evaluated.
Three
methods
for
analyses:
(1)
unadjusted
analysis,
(2)
stabilized
inverse
probability
weighting
(sIPTW;
primary
analysis),
(3)
propensity
score
matching
(PSM;
sensitivity
analysis).A
total
961
identified
who
started
(n
=
313)
or
648)
as
first-line
(1L)
therapy
between
February
2015
March
2020
(data
cut-off:
September
30,
2020).
Among
group
a
documented
starting
dose
306),
approximately
75%
at
125
mg/day,
40%
experienced
adjustment.
After
sIPTW,
had
significantly
improved
OS
(median
43.0
vs.
32.4
months;
hazard
ratio
[HR],
0.66
[95%
confidence
interval
(CI),
0.51-0.84];
P
0.0007),
rwPFS
20.0
15.0
HR,
0.72
(0.59-0.89);
0.0021),
TTC
40.2
27.4
0.69
[0.55-0.87];
0.0014).
These
significant
improvements
OS,
rwPFS,
remained
consistent
analysis
after
PSM.This
demonstrated
that
1L
is
associated
compared
years.
findings
support
standard-of-care
mBC.
Breast Cancer Research and Treatment,
Год журнала:
2024,
Номер
206(2), С. 337 - 346
Опубликована: Апрель 16, 2024
Abstract
Purpose
Palbociclib
has
become
the
standard
of
care
for
estrogen
receptor-positive
(ER+),
human
epidermal
growth
factor
receptor
2
negative
(HER2-)
metastatic
breast
cancer,
but
real-world
evidence
in
older
women
remains
scarce.
Therefore,
we
investigated
tolerability
palbociclib
with
cancer.
Methods
Consecutive
aged
≥
70
ER+/HER2-
treated
any
treatment
line
six
hospitals,
were
included.
Primary
endpoint
was
grade
3
palbociclib-related
toxicity.
Predictors
toxicity
identified
using
logistic
regression
models.
Progression-free
survival
(PFS)
and
overall
(OS)
estimated
Kaplan
Meier.
Results
We
included
144
a
median
age
74
years.
Grade
3–4
occurred
54%
patients,
which
neutropenia
(37%)
most
common.
No
neutropenic
fever
or
5
occurred.
Dose
reduction
during
50%
8%
discontinued
due
to
3%
hospitalized
Polypharmacy
(odds
ratio
(OR)
2.50;
95%
confidence
interval
(CI)
1.12–5.58)
pretreatment
low
leukocytes
(OR
4.81;
CI
1.27–18.21)
associated
toxicity,
while
comorbidities
not.
In
first-line
systemic
therapy,
PFS
12
months
OS
32
months.
second-line,
31
Conclusion
Although
dose
reductions
frequently,
expected
managed
by
reductions,
showing
that
is
generally
well
tolerated
thus
represents
valuable
option
population.
Frontiers in Oncology,
Год журнала:
2025,
Номер
15
Опубликована: Март 10, 2025
Aim
Since
2021,
additional
real-world
evidence
(RWE)
has
emerged
on
the
effectiveness
of
cyclin-dependent
kinase
4/6
inhibitors
(CDK4/6i)
as
first-line
treatment
HR-positive/HER2-negative
(HR+/HER2−)
advanced/metastatic
breast
cancer
(A/MBC),
necessitating
this
updated
review.
Methods
MEDLINE
®
,
Embase
and
Cochrane
Databases
(07/06/2019–01/09/2024),
key
congresses
(2020–2024)
were
searched.
Studies
reporting
CDK4/6i
use,
over
100
participants,
progression-free
survival
(PFS)
and/or
overall
(OS)
data
included.
Results
This
update
included
82
unique
studies,
42.7%
for
palbociclib,
7.3%
ribociclib,
3.7%
abemaciclib;
46.3%
assessed
multiple
CDK4/6i.
In
studies
including
CDK4/6is,
median
PFS
was
23.4–31.0
months
19.8–44.0
14.0–39.5
abemaciclib.
When
reached,
OS
38.0–58.0
months,
40.4–52.0
34.4
respectively.
These
results
within
range
single-arm
versus
endocrine
therapy
(ET)
where
demonstrated
greater
benefits
than
ET
alone.
Conclusion
First-line
RWE
demonstrates
significant
clinical
in
HR+/HER2−
A/MBC.
are
important
to
guide
decision-making,
they
include
patients
who
not
adequately
represented
trials.
with
longer
follow-up
needed
assess
long-term
all
three
therapies
ABSTRACT
Introduction
Cyclin‐dependent
kinase
4/6
inhibitors
(CDK4/6is)
in
combination
with
endocrine
therapy
are
the
current
standard
of
care
for
first‐line
(1L)
treatment
hormone
receptor–positive
and
human
epidermal
growth
factor
receptor
2–negative
(HR+/HER2–)
metastatic
breast
cancer
(mBC).
To
investigate
effectiveness
palbociclib,
first‐in‐class
CDK4/6i,
plus
an
aromatase
inhibitor
(AI)
older
patients,
we
compared
overall
survival
(OS)
a
Medicare
population
treated
1L
palbociclib
+
AI
versus
alone.
Methods
Patients
aged
≥
65
years
who
were
diagnosed
de
novo
HR+/HER2–
mBC
from
2015
to
2019
identified
Surveillance,
Epidemiology,
End
Results
(SEER)–linked
database
eligible
if
they
initiated
or
The
primary
endpoint
was
OS.
Stabilized
inverse
probability
weighting
(sIPTW)
used
balance
baseline
patient
characteristics.
Of
779
296
received
483
alone
as
treatment.
After
sIPTW,
median
follow‐up
23.1
months
18.2
Adjusted
OS
longer
(sIPTW:
37.6
vs.
25.5
months,
HR
=
0.73
[95%
CI,
0.59–0.91]).
In
multivariable
Cox
proportional
hazards
regression,
patients
had
39%
lower
risk
death
(HR
0.61
0.48–0.77]).
Conclusion
routine
US
clinical
practice,
associated
significantly
prolonged
mBC,
adding
growing
body
evidence
on
benefit
this
population.
Trial
Registration
ClinicalTrials.gov
identifier:
NCT06086340
Breast Cancer Research,
Год журнала:
2024,
Номер
26(1)
Опубликована: Окт. 18, 2024
This
study
used
real-world
observational
data
to
compare
profiles
of
patients
receiving
different
first-line
treatment
for
hormone
receptor
positive
(ER+),
HER2
negative,
metastatic
breast
cancer
(MBC):
CDK4/6
inhibitors
(CDK4/6i)
in
combination
with
endocrine
therapy
(ET)
versus
ET
alone.
From
a
nationwide
electronic
health
record-derived
Flatiron
Health
de-identified
database
including
280
US
clinics,
we
identified
positive,
1st
-line
alone
or
CDK4/6i
plus
between
February
2015
and
November
2021.
Patient
sociodemographic
status,
MBC
regimen
outcomes
were
the
focus
this
analysis.
characteristics
compared
using
t-tests
chi-square
tests.
Logistic
regression
analysis
was
performed
examine
association
patient
likelihood
vs.
Kaplan-Meier
method
Cox
proportional
hazards
test
impact
on
progression-free
survival
(PFS)
overall
(OS).
Baseline
balanced
inverse
probability
weighting
(IPW).
The
population
included
3,917
(n
=
2170)
1747)
their
MBC.
Compared
alone,
those
younger
(mean
age
66.8
68.6,
p
<
0.001),
more
likely
present
de
novo
(p
had
better
performance
status
(50.2%
40.5%
ECOG
value
0,
0.001)
lower
number
comorbidities
(29.7%
26.6%
≥
1
comorbidity,
0.001).
revealed
increased
odds
individuals
aged
50–64
(OR:
3.42,
95%
CI
[2.41,
4.86])
65–74
3.18,
[1.68,
6.02])
18–49
years
age.
Black
0.76,
[0.58,
1.00])
White
individuals.
Other
associated
stage
III
disease
0.69,
[0.52,
0.92]),
0.50,
[0.40,
0.62]),
Medicare
insurance
0.73,
[0.30,
1.78])
commercial
Medicaid
insurance.
After
IPW
adjustment,
use
as
significantly
longer
median
PFS
(27
17
months;
hazard
ratio
[HR]
0.61,
Median
OS
52
months
group
42
(HR
0.74,
In
database,
disparities
seen
by
age,
diagnosis
stage,
baseline
status.
adjusted
analysis,
yielded
rates
than
Further
efforts
are
essential
enhance
equitable
access
crucial
drug
class.