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