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Specialty Pharmacy Clinical Policy Bulletins
Aetna Non-Medicare Prescription Drug Plan
Subject: Kisqali 1639-A SGM P2023

Drug
KISQALI  (ribociclib)


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.  Kisqali is indicated in combination with an aromatase
                    inhibitor as initial endocrine-based therapy for the
                    treatment of adult patients with hormone receptor (HR)-
                    positive, human epidermal growth factor receptor 2
                    (HER2)-negative advanced or metastatic breast cancer.

               2.  Kisqali is indicated in combination with fulvestrant for the
                    treatment of postmenopausal women or in men with
                    (HR)-positive, human epidermal growth factor receptor 2
                    (HER2)-negative advanced or metastatic breast cancer, as
                    initial endocrine based therapy or following disease
                    progression on endocrine therapy.

          B.  Compendial Uses
               Breast cancer: Recurrent HR-positive, HER2-negative
               disease.

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


    II.  DOCUMENTATION

          Submission of hormone receptor (HR) and human epidermal
          growth factor receptor 2 (HER2) status is necessary to initiate
          the prior authorization review.

 
  III.  CRITERIA FOR INITIAL APPROVAL

          Breast cancer
          Authorization of 12 months may be granted to members for
          treatment of HR-positive, HER2-negative recurrent, advanced,
          or metastatic breast cancer when used in combination with an
          aromatase inhibitor or fulvestrant.

 
  IV.   CONTINUATION OF THERAPY

          Authorization of 12 months may be granted for continued
          treatment in members requesting reauthorization for an
          indication outlined 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. Kisqali [package insert]. East Hanover, NJ: Novartis Pharmaceuticals Corporation; October 2022.
  2. The NCCN Drugs & Biologics Compendium® © 2022 National Comprehensive Cancer Network, Inc. Available at: http://www.nccn.org. Accessed November 8, 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.

June 18, 2023
Aetna
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