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CD30 targeting with brentuximab vedotin: a novel therapeutic approach to primary effusion lymphoma.
[primary effusion lymphoma]
Primary
effusion
lymphoma
(
PEL
)
is
an
aggressive
subtype
of
non-
Hodgkin
lymphoma
characterized
by
short
survival
with
current
therapies
,
emphasizing
the
urgent
need
to
develop
new
therapeutic
approaches
.
Brentuximab
vedotin
(
SGN-
35
)
is
an
anti-
CD
30
monoclonal
antibody
(
cAC
10
)
conjugated
by
a
protease-cleavable
linker
to
a
microtubule-disrupting
agent
,
monomethyl
auristatin
E
.
Brentuximab
vedotin
is
an
effective
treatment
of
relapsed
CD
30
-
expressing
Classical
Hodgkin
and
systemic
anaplastic
large
cell
lymphomas
.
Herein
,
we
demonstrated
that
PEL
cell
lines
and
primary
tumors
express
CD
30
and
thus
may
serve
as
potential
targets
for
brentuximab
vedotin
therapy
.
In
vitro
treatment
with
brentuximab
vedotin
decreased
cell
proliferation
,
induced
cell
cycle
arrest
,
and
triggered
apoptosis
of
PEL
cell
lines
.
Furthermore
,
in
vivo
brentuximab
vedotin
promoted
tumor
regression
and
prolonged
survival
of
mice
bearing
previously
reported
UM-
PEL
-
1
tumors
as
well
as
UM-
PEL
-
3
tumors
derived
from
a
newly
established
and
characterized
Kaposi
's
sarcoma
-associated
herpesvirus-
and
Epstein-
Barr
virus-
positive
PEL
cell
line
.
Overall
,
our
results
demonstrate
for
the
first
time
that
brentuximab
vedotin
may
serve
as
an
effective
therapy
for
PEL
and
provide
strong
preclinical
indications
for
evaluation
of
brentuximab
vedotin
in
clinical
studies
of
PEL
patients
.
Diseases
Validation
Diseases presenting
"first time"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
congenital adrenal hyperplasia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
gm1 gangliosidosis
harlequin ichthyosis
heparin-induced thrombocytopenia
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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