Rye Brook, N.Y. (December
18, 2020) – The U.S. Food and Drug Administration (FDA) today announced
approval of selinexor (Xpovio®) for adults with multiple myeloma who
have had at least one prior type of treatment. Selinexor is used in combination
with the chemotherapy drug bortezomib (Velcade®) and the
corticosteroid dexamethasone in these patients.
LLS supported development
of selinexor with over $4 million in grants for research in multiple myeloma
and other forms of blood cancer. Despite therapeutic advances, there is no cure
for multiple myeloma and a pressing need for additional treatment options for
patients who are living with this progressive disease. Multiple myeloma
accounts for nearly one in five new blood cancer diagnoses in the United States
each year, with most of the 30,000 new cases diagnosed in people in their
mid-60s.
Today’s approval expands
the availability of selinexor to patients in earlier stages of multiple
myeloma. Selinexor was previously approved for patients whose multiple myeloma
had returned or was progressing despite treatment with at least four prior
therapies. Selinexor is an oral therapy that works by helping the body’s cells
retain proteins they need to fight cancer.
The approval was based on
results from the phase 3 BOSTON study. Patients who received treatment
once-a-week with a combination of selinexor, bortezomib and dexamethasone had a
47% improvement in progression-free survival (PFS) compared to patients on the
standard twice-a-week treatment with bortezomib and dexamethasone with a median
PFS of 13.9 months compared to 9.4 months. The triple combination patients had
fewer clinic visits and received less of the chemotherapy and steroid drugs
overall. However, the combination treatment is associated with some serious,
though usually manageable side effects. A full report on this study has been
published (Grosicki et al., 2020. Lancet 396: 1563-1573).
LLS continues to support
the development of new life-extending therapies for patients with multiple
myeloma by funding the best foundational research as well as clinical studies
through our robust academic grant and venture philanthropy programs.
https://www.lls.org/news/fda-approval-treatment-advance-for-patients-with-multiple-myeloma
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