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Specialty Pharmacy Clinical Policy Bulletins
Aetna Non-Medicare Prescription Drug Plan
Subject: Alunbrig 1815-A SGM P2022

Drug
ALUNBRIG  (brigatinib)


Policy:

       I.  INDICATIONS

            The indications below including FDA-approved indications and
            compendial uses are considered a covered benefit provided
            that all the approval criteria are met and the member has no
            exclusions to the prescribed therapy.

            A.  FDA-Approved Indication
                Alunbrig is indicated for the treatment of adult patients with
                anaplastic lymphoma kinase (ALK)-positive metastatic non
                small cell lung cancer (NSCLC) as detected by an FDA-
                approved test.

            B. Compendial Uses
                1.  Recurrent, advanced or metastatic ALK rearrangement-
                     positive NSCLC as a single agent
                2.  Brain metastases from ALK rearrangement-positive
                     NSCLC as a single agent
                3.  Inflammatory myofibroblastic tumor (IMT) with ALK
                     translocation as a single agent

            All other indications are considered
            experimental/investigational and not medically necessary.

 
      II.  DOCUMENTATION

            Submission of the following information is necessary to initiate
            the prior authorization review: ALK mutation status

 
    III.  CRITERIA FOR INITIAL APPROVAL

            A.  Non-Small Cell Lung Cancer (NSCLC)
                 Authorization of 12 months may be granted for treatment
                 of recurrent, advanced, or metastatic ALK-positive NSCLC
                 (including brain metastases from NSCLC) as a single agent.

            B.  Inflammatory Myofibroblastic Tumor (IMT)
                 Authorization of 12 months may be granted for treatment
                 of ALK-positive IMT as a single agent.

 
     IV.  CONTINUATION OF THERAPY

            A.  Non-Small Cell Lung Cancer (NSCLC)
                 Authorization of 12 months may be granted for continued
                 treatment in members requesting reauthorization when
                 there is no evidence of unacceptable toxicity while on the
                 current regimen.

            B.  Inflammatory Myofibroblastic Tumor (IMT)
                 Authorization of 12 months may be granted for continued
                 treatment in members requesting reauthorization when
                 there is no evidence of unacceptable toxicity or disease
                 progression while on the current regimen.

 

 


Place of Service:

Outpatient

The above policy is based on the following references:
  1. Alunbrig [package insert]. Lexington, MA: Takeda Pharmaceuticals America, Inc.; February 2022.
  2. The NCCN Drugs & Biologics Compendium® © 2022 National Comprehensive Cancer Network, Inc. https://www.nccn.org. Accessed March 9, 2022.
Copyright Aetna Inc. All rights reserved. Pharmacy Clinical Policy Bulletins are developed by Aetna to assist in administering plan benefits and constitute neither offers of coverage nor medical advice. This Clinical Policy Bulletin contains only a partial, general description of plan or program benefits and does not constitute a contract. Aetna does not provide health care services and, therefore, cannot guarantee any results or outcomes. Participating providers are independent contractors in private practice and are neither employees nor agents of Aetna or its affiliates. Treating providers are solely responsible for medical advice and treatment of members. This Clinical Policy Bulletin may be updated and therefore is subject to change.

August 24, 2022
Aetna
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