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[Results of adjuvant chemotherapy (XELOX) of advanced colorectal cancer].
[papillon-lefèvre syndrome]
While
the
most
frequent
,
surgery
for
colorectal
cancer
is
avoided
in
patients
with
metastases
to
the
regional
lymph
nodes
(
stage
III
)
or
distant
ones
(
stage
IV
)
.
Hence
,
it
is
being
increasingly
substituted
with
neoadjuvant
treatment
.
Our
investigation
is
concerned
with
prospective
evaluation
of
the
efficacy
and
toxicity
profile
of
capecitabine
(
XELODA
)
in
combination
with
oxaliplatin
(
XELOX
)
and
adjuvant
Mayo
treatment
(
stage
IIb-
III
)
.
Patients
had
undergone
radical
surgery
(
somatic
status
<
or
=
2
-
ECOG
)
.
The
prospective
group
(
166
)
received
8
courses
of
adjuvant
polychemotherapy
(
XELOX
)
;
the
retrospective
(
2001
-
2005
)
one
(
152
)
-
-
6
(
Mayo
)
.
The
groups
matched
one
another
as
far
as
number
,
gender
,
age
and
primary
tumor
localization
are
concerned
.
Regional
lymph
node
involvement
in
group
1
was
64
.
5
%
;
group
2
-
-
59
.
8
%
.
Lympho-
vascular
invasion
by
tumor
was
typical
of
group
1
;
gastrointestinal
toxicity
-
9
.
2
%
(
Mayo
)
vs
.
7
.
2
%
in
group
1
.
Hematological
complications
were
5
.
4
%
(
XELOX
)
and
5
.
3
%
(
Mayo
)
;
neutropenia
--
5
.
0
%
(
Mayo
)
and
3
.
0
%
(
XELOX
)
;
polyneutropenia--
3
.
6
%
(
XELOX
)
;
capecitabine-related
Papillon-
Lefevre
syndrome--
8
.
4
%
.
Three
-
year
relapse-free
survival
was
53
.
0
%
(
XELOX
)
and
47
.
5
%
(
Mayo
)
.
After
adjuvant
treatment
,
toxicity
profile
with
XELOX
was
lower
than
that
after
Mayo
,
with
the
survival
tending
to
improve
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated