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