Aetna
Aetna Aetna
Specialty Pharmacy Clinical Policy Bulletins
Aetna Non-Medicare Prescription Drug Plan
Subject: Xtandi 1933-A SGM P2022

Drug
XTANDI  (enzalutamide)


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.

            FDA-Approved Indications
            Xtandi is indicated for the treatment of patients with:
            A.  Castration-resistant prostate cancer (CRPC)
            B.  Metastatic castration-sensitive prostate cancer (mCSPC)

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

 
     II.  EXCLUSIONS

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

 
    III.  CRITERIA FOR INITIAL APPROVAL

            A.  Castration-resistant prostate cancer (CRPC)
                 Authorization of 12 months may be granted for the
                 treatment of castration-resistant prostate cancer when the
                 member has had a bilateral orchiectomy or will be using the
                 requested medication in combination with a GnRH analog.

            B.  Metastatic castration-sensitive prostate cancer
                 (mCSPC)
                 Authorization of 12 months may be granted for the
                 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 GnRH
                 analog.

 
     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. Xtandi [package insert]. Northbrook, IL: Astellas Pharma US, Inc.; January 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.

December 29, 2022
Aetna
Skip Past Footer Links
Company Information   |   Site Map Aetna.com Home   |   Help   |   Contact Us   |   Search
Web Privacy Statement   |   Legal Statement   |   Privacy Notices   |   Member Disclosure

Back to top