Kimmtrak (tebentafusp) - CAM 934HB
Background
Kimmtrak is a medication used to treat a specific type of eye cancer called uveal melanoma. It is a bispecific protein that helps the body's immune system attack cancer cells. Specifically, it is used for patients with HLA-A*02:01-positive unresectable or metastatic uveal melanoma.
Policy (Criteria)
Kimmtrak (tebentafusp) is considered MEDICALLY NECESSARY when the following criteria are met:
-
- Provider attestation that patient has HLA-A*02:01-positive uveal melanoma, AND
- Disease is unresectable or metastatic, AND
- Being used as single agent therapy
Approval duration: 6 months
Continuation of Kimmtrak is considered MEDICALLY NECESSARY when there is documentation that member is responsive to therapy with no disease progression.
Approval duration: 12 months
Covered Doses
Dose maximum of 20 mcg IV on Day 1, 30 mcg IV on Day 8, 68 mcg IV on Day 15, and 68 mcg IV once every week thereafter.
References
- AHFS®. Available by subscription at http://www.lexi.com
- DrugDex®. Available by subscription at http://www.micromedexsolutions.com
- Kimmtrak® (tebentafusp-tebn) [Prescribing Information]. Conshohocken, PA: Immunocore Commercial LLC.; 1/2022.
- National Comprehensive Cancer Network. Melanoma: Uveal (Version 2.2022). Available at: www.nccn.org/
- Kimmtrak® Billing and Code Guide. Available at https://kimmtrakhcp.com/pdf/KIMMTRAK-billing-and-coding-guide.pdf
Coding Section
Procedure and diagnosis codes on Medical Policy documents are included only as a general reference tool for each Policy. They may not be all-inclusive.
Code |
Number |
Description |
HCPCS |
J9274 |
Injection, tebentafusp-tebn, 1 microgram |
CPT |
96413 |
Chemotherapy administration, intravenous infusion technique; up to 1 hour, single or initial substance/drug |
|
96409 |
Chemotherapy administration, intravenous, push technique; single or initial substance/drug |
This medical policy was developed through consideration of peer-reviewed medical literature generally recognized by the relevant medical community, U.S. FDA approval status, nationally accepted standards of medical practice and accepted standards of medical practice in this community, technology assessment program (TEC) and other non-affiliated technology evaluation centers, reference to federal regulations, other plan medical policies, and accredited national guidelines.
"Current Procedural Terminology © American Medical Association. All Rights Reserved"
History From 2025 Forward
07/01/2025 |
New Policy |