I. 
Initial Approval Criteria 
 
A. 
Diffuse Large B-Cell Lymphoma 
(must meet all): 
1. 
Diagnosis of DLBCL (see subtypes at Appendix D); 
2. 
Prescribed by or in consultation with an oncologist or hematologist; 
3. Age 
≥ 18 years; 
4. 
Member is not a candidate for allogeneic or autologous stem cell transplant; 
5. 
Member has received ≥ 1 prior therapy; 
6. 
Polivy is prescribed as a single agent or in combination with bendamustine* 
and/or a rituximab product* ; 
*Prior authorization may be 
required for bendamustine and rituximab products 
 
7. 
Request meets one of the following (a or b):* 
a. Dose does not exceed 
1.8 mg/kg on Day 1 of a 21-day cycle, for a maximum of 6 cycles; 
b. Dose is supported by 
practice guidelines or peer-reviewed literature for the relevant off-label use (prescriber 
must submit supporting evidence). 
*Prescribed regimen must be 
FDA-approved or recommended by NCCN. 
Approval duration: 6 months (medical justification supports requests for 
cycles beyond 6)
 
 
B. 
NCCN Recommended Uses (off-label) 
(must meet all): 
1. 
Diagnosis of one of the following (a, b, c, d, or e): 
a. Follicular lymphoma 
(FL) (grade 1-2); 
b. Mantle cell lymphoma; 
c. Monomorphic 
post-transplant lymphoproliferative disorder (B-cell type); 
d. One of the following 
AIDS-related B-cell lymphoma subtypes (i, ii, iii, or iv):
i. AIDS-related DLBCL; 
ii. Primary effusion 
lymphoma; 
iii. HHV8-positive 
diffuse large B-cell lymphoma, NOS; 
iv. AIDS-related 
plasmablastic lymphoma;
e. Histologic 
transformation of nodal marginal zone lymphoma to diffuse large B-cell lymphoma; 
2. 
Prescribed by or in consultation with an oncologist or hematologist; 
3. Age 
≥ 18 years; 
4. For 
requests other than FL grade 1-2, member is not a candidate for allogeneic or 
autologous stem cell transplant; 
5. 
Member has received ≥ 1 prior therapy; 
6. 
Polivy is prescribed as a single agent or in combination with bendamustine* 
and/or a rituximab product* ; 
*Prior 
authorization may be required for bendamustine and rituximab products 
 
7. 
Dose is within FDA maximum limit for any FDA-approved indication or is supported 
by practice guidelines or peer-reviewed literature for the relevant off-label 
use (prescriber must submit supporting evidence).* 
 
*Prescribed regimen must be FDA-approved or recommended by NCCN 
Approval duration: 6 months (medical justification is required for requests 
for more than 6 cycles)
 
 
II. 
Continued Therapy 
A. 
All Indications in Section I 
(must meet all): 
1. 
Currently receiving medication via QualChoice benefit, or documentation supports 
that member is currently receiving Polivy for a covered indication and has 
received this medication for at least 30 days; 
 
2. 
Member is responding positively to therapy; 
3. 
Member meets one of the following (a or b): 
a. Member has received < 
6 cycles of Polivy; 
b. Member has received 
less than the number of cycles recommended by NCCN for the covered indication; 
4. If 
request is for a dose increase, request meets one of the following (a or b):* 
a. New dose does not 
exceed 1.8 mg/kg on Day 1 of a 21-day cycle, for a maximum of 6 cycles; 
b. New dose is supported 
by practice guidelines or peer-reviewed literature for the relevant off-label 
use (prescriber must submit supporting evidence).
 
*Prescribed regimen must be FDA-approved or recommended by NCCN. 
Approval duration: 12 months (medical justification supports requests for 
cycles beyond 6)
 
 
Codes 
Used In This BI:
 
1)   
J9309 Injection, 
polatuzumab vedotin-piiq