Initial Approval Criteria
I.
Multiple Myeloma (must
meet all):
a.
Diagnosis of MM;
b.
Prescribed by or in
consultation with an oncologist or hematologist;
c.
Age > 18 years;
d.
Disease is relapsed or
refractory;
e.
One of the following (i
or ii):
i.
Member has measurable
disease as evidenced by one of the following assessed:
1.
Serum M-proten >
5g/dL;
2.
Urine M-protein >
200 mg/23h;
3.
Serum free light chain
(FLC) assay: involved FLC level > 10mg/dL (100mg/L) provided serum FLC
ratio is abnormal;
ii.
Member has progressive
disease, as defined by the IMWG response criteria assessed with 60 days
following the last dose of the last anti-myeloma drug regimen received.
f.
Elrexfio is prescribed as
monotherapy;
g.
Member has received or
has documented intolerance to > 4 prior lines of therapy that include all
of the following:
i.
One proteasome inhibitor
(e.g. bortezomib, Kyprolis, Ninlaro)
ii.
One immunomodulatory drug
(e.g. Revlmid, pomalidomide, Thalomid)
iii.
One anti-CD38 antibody
(e.g. Darzalex/Darzalex Faspro), Sarclisa)
h.
Dose is consistent with
FDA labeling
Approval Duration: 6 months
Continued Therapy Criteria
1.
Member is responding
positively to therapy
2.
Dose is consistent with
FDA labeling.
Continued Therapy Duration: 12 months