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Specialty Pharmacy Clinical Policy Bulletins
Aetna Non-Medicare Prescription Drug Plan
Subject: Erleada 2498-A SGM P2024

Drug
ERLEADA  (apalutamide)


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 Indications
               1.  Erleada is indicated for the treatment of patients with non-metastatic castration-resistant
                    prostate cancer.
               2.  Erleada is indicated for the treatment of patients with metastatic castration-sensitive
                    prostate cancer.

          B.  Compendial Use
               Prostate Cancer

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


   III.  EXCLUSIONS

          Coverage will not be provided if the requested medication is used in combination with a
          second-generation oral anti-androgen (e.g., enzalutamide [Xtandi]) or an oral androgen
          metabolism inhibitor (e.g., abiraterone acetate [Zytiga]).


   III.  CRITERIA FOR INITIAL APPROVAL

          1.  Non-metastatic castration-resistant prostate cancer
               Authorization of 12 months may be granted for treatment of non-metastatic castration-
               resistant prostate cancer when the member has had a bilateral orchiectomy or will be using
               the requested medication in combination with a luteinizing hormone-releasing hormone
               (LHRH) agonist (e.g., goserelin, leuprolide) or antagonist (e.g., degarelix, relugolix).

          2.  Metastatic castration-sensitive prostate cancer
               Authorization of 12 months may be granted for treatment of metastatic castration-sensitive
               prostate cancer when the member has had a bilateral orchiectomy or will be using the
               requested medication in combination with a luteinizing hormone-releasing hormone (LHRH)
               agonist (e.g., goserelin, leuprolide) or antagonist (e.g., degarelix, relugolix).


   IV.  CONTINUATION OF THERAPY

          Authorization of 12 months may be granted for continued treatment in members requesting
          reauthorization for an indication listed in Section III 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. Erleada [package insert]. Horsham, PA: Janssen Products, LP; December 2023.
  2. The NCCN Drugs & Biologics Compendium™ © 2024 National Comprehensive Cancer Network, Inc. https://www.nccn.org Accessed July 2, 2024.

 

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.

November 03, 2024
Aetna
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