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Specialty Pharmacy Clinical Policy Bulletins
Aetna Non-Medicare Prescription Drug Plan
Subject: Inqovi 4002-A SGM P2023

Drug
INQOVI  (decitabine and cedazuridine)


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
               Inqovi is indicated for treatment of adult patients with
               myelodysplastic syndromes (MDS), including previously
               treated and untreated, de novo and secondary MDS with
               the following French-American-British subtypes (refractory
               anemia, refractory anemia with ringed sideroblasts,
               refractory anemia with excess blasts, and chronic
               myelomonocytic leukemia [CMML]) and intermediate-1,
               intermediate-2, and high-risk International Prognostic
               Scoring System groups.

          B.  Compendial Use
               Myelodysplastic syndrome/myeloproliferative neoplasm
               (MDS/MPN) overlap neoplasm

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


    II.  CRITERIA FOR INITIAL APPROVAL

     A.  Myelodysplastic syndromes (MDS)
          Authorization of 12 months may be granted for the treatment
          of myelodysplastic syndromes (MDS).

          B.  Myelodysplastic syndrome/myeloproliferative
          neoplasm (MDS/MPN) overlap neoplasms
          Authorization of 12 months may be granted for the treatment of
          MDS/MPN overlap neoplasms (i.e., chronic myelomonocytic
          leukemia (CMML), BCR-ABL negative atypical chronic myeloid
          leukemia (aCML), MDS/MPN with neutrophilia, unclassifiable
          MDS/MPN, or MDS/MPN with ring sideroblasts and
          thrombocytosis). 


  III.  CONTINUATION OF THERAPY

          Authorization of 12 months may be granted for continued
          treatment in members requesting reauthorization for an
          indication listed in Section II 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. Inqovi [package insert]. Princeton, NJ: Taiho Oncology, Inc; March 2022.
  2. The NCCN Drugs & Biologics Compendium® © 2023 National Comprehensive Cancer Network, Inc. Available at http://www.nccn.org. Accessed January 7, 2023.
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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