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A retrospective study of docetaxel or paclitaxel in patients with advanced or recurrent esophageal squamous cell carcinoma who previously received fluoropyrimidine- and platinum-based chemotherapy.
[esophageal squamous cell carcinoma]
Fluoropyrimidine
plus
platinum
(
FP
)
-
based
chemotherapy
has
been
widely
used
as
a
first
-line
regimen
for
advanced
or
recurrent
esophageal
cancer
,
and
taxanes
have
shown
efficacy
after
FP-based
chemotherapy
,
but
there
is
no
standard
regimen
for
second
-line
chemotherapy
(
SLC
)
.
We
retrospectively
investigated
the
clinical
features
of
taxane
therapy
in
SLC
for
esophageal
squamous
cell
carcinoma
(
ESCC
)
.
The
selection
criteria
were
pathologically
proven
ESCC
;
advanced
or
recurrent
disease
previously
treated
with
FP
at
our
hospital
;
performance
status
(
PS
)
0
-
2
;
and
adequate
organ
function
.
Docetaxel
(
DTX
)
was
administered
3
-
weekly
at
70
Â
mg
/
m
(
2
)
.
Paclitaxel
(
PTX
)
was
administered
at
100
Â
mg
/
m
(
2
)
weekly
for
6
Â
weeks
,
with
1
Â
week
's
rest
.
The
analysis
covered
163
patients
from
August
2006
to
June
2012
.
Median
age
was
64
Â
years
(
range
37
-
83
:
DTX
group
132
patients
and
PTX
group
31
)
.
Progression-free
survival
and
median
overall
survival
(
OS
)
were
2
.
3
and
6
.
1
Â
months
,
respectively
,
with
PTX
and
2
.
3
and
5
.
3
Â
months
with
DTX
.
Response
rates
were
20
.
7
Â
%
for
PTX
and
5
.
9
Â
%
for
DTX
.
The
rate
of
grades
3
-
4
neutropenia
was
higher
with
DTX
(
32
.
6
Â
%
)
than
with
PTX
(
16
.
1
Â
%
)
.
Grade
3
febrile
neutropenia
was
seen
in
6
.
1
Â
%
of
DTX
recipients
but
in
no
PTX
group
.
According
to
multivariate
analyses
of
OS
,
PS
2
,
number
of
metastatic
sites
≧
2
,
and
CRP
≧
1
Â
mg
/
dL
were
independent
predictors
of
poor
prognosis
.
PTX
and
DTX
were
both
effective
in
SLC
for
ESCC
,
but
their
toxicity
profiles
differed
.
In
terms
of
febrile
neutropenia
,
PTX
seems
more
appropriate
.
Diseases
Validation
Diseases presenting
"recurrent disease"
symptom
acute rheumatic fever
cholangiocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
junctional epidermolysis bullosa
pleomorphic liposarcoma
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