Shortcoming of serum B-cell maturation antigen measurement by enzyme-linked immunosorbent assay in one laboratory’s experience: Unsatisfactory assay reproducibility
Clinical Biochemistry,
Journal Year:
2025,
Volume and Issue:
138, P. 110941 - 110941
Published: May 8, 2025
Language: Английский
Research progress of targeted BCMA CAR-T therapy for relapsed/refractory multiple myeloma antigen-negative relapse
Best Practice & Research Clinical Haematology,
Journal Year:
2025,
Volume and Issue:
unknown, P. 101632 - 101632
Published: May 1, 2025
Language: Английский
CAR-T Therapy in Multiple Myeloma: Looking Beyond
Gianluca Maiorana,
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Giusy Antolino,
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Giacinto La Verde
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et al.
Hemato,
Journal Year:
2024,
Volume and Issue:
5(2), P. 180 - 198
Published: May 31, 2024
Multiple
Myeloma
is
a
hematological
neoplasm
that,
over
the
recent
few
years,
has
benefited
from
numerous
therapeutic
options.
Among
latter,
CAR-T
stands
out
as
most
and
one
of
promising
treatments
currently
available.
Despite
its
introduction,
multiple
products
have
already
been
approved,
research
regarding
cellular
therapy
rapidly
increasing.
We
conducted
comprehensive
search
review
available
literature,
including
published
studies
abstracts
meetings
(ASH,
ASCO,
ASTCT,
IMS),
therapy.
describe
discovery
targets
like
B-Cell
Maturation
Antigen
(BCMA)
others,
origin
nature
cells,
introduction
anti-BCMA
CAR-Ts
Idecabtagene-vicleucel
Ciltacabtagene-autoleucel,
which
are
only
approved
for
MM.
Additionally,
we
discuss
non-BCMA-targeting
their
clinical
implications.
Given
significant
impact
therapy,
provide
an
overview
limitations
possible
adverse
implications,
well
related
resistance
mechanisms.
Finally,
current
aimed
at
improving
in
MM,
structural
innovations
new
approaches,
such
earlier
lines
treatment
maintenance
Language: Английский
Measurable Residual Disease Testing in Multiple Myeloma Following T-Cell Redirecting Therapies
Cancers,
Journal Year:
2024,
Volume and Issue:
16(19), P. 3288 - 3288
Published: Sept. 27, 2024
Several
novel
T-cell-based
therapies
have
recently
become
available
for
multiple
myeloma
(MM).
These
T-cell
redirecting
(TRTs)
include
chimeric
antigen
receptor
T-cells
(CAR-T)
and
bispecific
antibodies
(BiAbs).
In
both
clinical
trial
real-world
data,
these
demonstrated
high
rates
of
deep
response,
some
are
now
approved
second-line
treatment
relapsed
MM.
The
sustained
responses
capable
inducing
will
require
sophisticated
response
monitoring
to
provide
meaningful
information
patient
care.
Obtaining
measurable
residual
disease
(MRD)
negativity
has
been
validated
as
an
independent
positive
prognostic
marker
progression-free
survival
(PFS)
overall
(OS)
in
newly
diagnosed
refractory
patients
with
myeloma.
Assessment
MRD
was
performed
all
the
trials
FDA-approved
TRT.
Here,
we
summarize
pertinent
data
assessment
following
TRT
MM
a
rationale
structured
framework
conducting
testing
post
Language: Английский