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Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency.
[severe combined immunodeficiency]
Patients
with
severe
combined
immunodeficiency
disease
who
have
matched
sibling
donors
(
MSDs
)
can
proceed
to
hematopoietic
cell
transplantation
(
HCT
)
without
conditioning
chemotherapy
.
We
sought
to
determine
whether
the
results
of
HCT
without
chemotherapy-based
conditioning
from
matched
unrelated
donors
(
URDs
)
,
either
from
volunteer
adults
or
umbilical
cord
blood
,
are
comparable
with
those
from
MSDs
.
We
performed
a
multicenter
survey
of
severe
combined
immunodeficiency
transplantation
centers
in
North
America
,
Europe
,
and
Australia
to
compile
retrospective
data
on
patients
who
have
undergone
unconditioned
HCT
from
either
URDs
(
n
=
37
)
or
MSDs
(
n
=
66
)
.
Most
patients
undergoing
URD
HCT
(
92
%
)
achieved
donor
T
-
cell
engraftment
compared
with
97
%
for
those
with
MSDs
;
however
,
estimated
5
-
year
overall
and
event-free
survival
were
worse
for
URD
recipients
(
71
%
and
60
%
,
respectively
)
compared
with
MSD
recipients
(
92
%
and
89
%
,
respectively
;
P
<
.
01
for
both
)
.
URD
recipients
who
received
pre-
HCT
serotherapy
had
similar
5
-
year
overall
survival
(
100
%
)
to
MSD
recipients
.
The
incidences
of
grade
II
to
IV
acute
and
chronic
graft-versus-host
disease
were
higher
in
URD
(
50
%
and
39
%
,
respectively
)
compared
with
MSD
(
22
%
and
5
%
,
respectively
)
recipients
(
P
<
.
01
for
both
)
.
In
the
surviving
patients
there
was
no
difference
in
T
-
cell
reconstitution
at
the
last
follow-up
between
the
URD
and
MSD
recipients
;
however
,
MSD
recipients
were
more
likely
to
achieve
B-
cell
reconstitution
(
72
%
vs
17
%
,
P
<
.
001
)
.
Unconditioned
URD
HCT
achieves
excellent
rates
of
donor
T
-
cell
engraftment
similar
to
that
seen
in
MSD
recipients
,
and
reconstitution
rates
are
adequate
.
However
,
only
a
minority
will
have
myeloid
and
B-
cell
reconstitution
,
and
attention
must
be
paid
to
graft-versus-host
disease
prophylaxis
.
This
approach
might
be
safer
in
children
ineligible
for
intense
regimens
to
spare
the
potential
complications
of
chemotherapy
.
Diseases
Validation
Diseases presenting
"chronic graft-versus-host disease"
symptom
severe combined immunodeficiency
systemic capillary leak syndrome
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