Mount Sinai researchers have
published results that show encouraging therapeutic options for
patients with the blood cancer multiple myeloma after first-line
treatment with bispecific antibodies fails. Bispecific antibodies
are a type of antibody that can bind to two different antigens at
the same time—they are meant to enhance the immune system's
destruction of tumor cells.
NEW
YORK, Sept. 1, 2022 /PRNewswire-PRWeb/ --
Mount Sinai researchers have
published results that show encouraging therapeutic options for
patients with the blood cancer multiple myeloma after first-line
treatment with bispecific antibodies fails. Bispecific antibodies
are a type of antibody that can bind to two different antigens at
the same time—they are meant to enhance the immune system's
destruction of tumor cells.
While new T cell-based immunotherapies, or "T-cell redirection"
therapies, such as chimeric antigen receptor (CAR) T-cell therapy
and bispecific antibodies have revolutionized cancer treatment,
doctors still need to determine what second-line treatments (also
known as salvage therapy) are effective after a patient relapses.
In the August 26 online edition of
Blood Advances , Mount Sinai
researchers report that sequential use of different T-cell
redirection therapies in these multiple myeloma patients is
possible and could lead to good patient outcomes and survival.
In a retrospective analysis, researchers identified 58 multiple
myeloma patients who participated in a bispecific antibodies
clinical trial at Mount Sinai and
underwent salvage therapy due to relapse. Patients were followed
for an average of 30.5 months after the end of the trial and
underwent an average of two salvage therapies over that period.
Nineteen patients received T-cell redirection therapy as a first
salvage therapy, and the rest received a non-T-cell redirection
therapy, such as chemotherapy. Thirty-two percent of patients who
underwent T-cell redirection therapy as a first salvage therapy
needed to undergo a second salvage therapy due to relapse or
nonresponse to therapy. In a significant contrast, 79 percent of
the patients treated with a non-T-cell redirection therapy needed
to undergo a second salvage therapy. Some of this group of patients
had T-cell redirection therapy as their second salvage therapy,
resulting in a total of 28 patients who received T-cell redirection
as either a first salvage therapy or second salvage therapy.
Depth and duration of response to the first bispecific
antibodies treatment did not predict response to the second T-cell
redirection therapy, indicating that even if patients did not
respond to an initial T-cell redirection therapy, there may still
be an option to effectively treat with a second course. The overall
response rate of the 19 patients who transitioned from the initial
bispecific antibodies to T-cell redirection therapy as a first
salvage therapy was 84 percent, compared to 49 percent in those who
received other types of therapies.
"As the clinical use and advancement of T-cell redirection
therapies continue to grow, effective strategies are needed to
manage outcomes for patients who relapse or are unresponsive to
this initial treatment," said senior author Samir Parekh, MD, Director of Translational
Research in Myeloma, co-leader of the Cancer Clinical Investigation
program at The Tisch Cancer Institute, and a member of the Icahn
Genomics Institute at the Icahn School of Medicine at Mount Sinai. "This study shows patients
relapsing after initial bispecific antibodies therapy can benefit
from a second bispecific antibody or CAR-T cell therapy."
Studies are underway to understand how T cells function after
initial T-cell redirection therapy and how they are activated in
sequential bispecific antibodies and CAR-T cell treatments. "Future
clinical trials incorporating sequential combinations of T-cell
redirection therapy will build upon these findings to further
develop treatment guidelines and improve long-term outcomes for
multiple myeloma patients," Dr. Parekh said.
This work was supported by the National Cancer Institute (NCI)
R01 CA244899 and CA252222.
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Media Contact
Karin Eskenazi, Mount Sinai
Health System, 332-257-1538, Karin.Eskenazi@mssm.edu
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SOURCE Mount Sinai Health System