Lyfgenia (lovotibeglogene autotemcel)

Indications for Prior Authorization

Lyfgenia (lovotibeglogene autotemcel)
  • For diagnosis of Sickle Cell Disease
    Indicated for the treatment of patients 12 years of age or older with sickle cell disease and a history of vaso-occlusive events.

    Limitations of Use: Following treatment with LYFGENIA, patients with α-thalassemia trait (-α3.7/-α3.7) may experience anemia with erythroid dysplasia that may require chronic red blood cell transfusions. Lyfgenia has not been studied in patients with more than two α-globin gene deletions.

Criteria

Lyfgenia

*Per prescribing information, Lyfgenia is for one-time, single dose intravenous use only.

Prior Authorization

Length of Approval: 1 Time Authorization in Lifetime*

  • Diagnosis of sickle cell disease (SCD)
  • AND
  • Patient has genotype βS/βS, βS/β0, or βS/β+ [2]
  • AND
  • Patient is 12 years of age or older
  • AND
  • Provider attests that patient is clinically stable and eligible to undergo hematopoietic stem cell transplant (HSCT)
  • AND
  • Patient has a history of at least 4 vaso-occlusive events (VOEs) in the past 24 months defined by one of following scenarios:
    • an episode of acute pain with no medically determined cause other than vaso-occlusion, lasting more than 2 hours
    • acute chest syndrome (ACS)
    • acute hepatic sequestration
    • acute splenic sequestration
    • VOE requiring a hospitalization or multiple visits to an emergency department/urgent care over 72 hours and receiving intravenous medications at each visit
    • priapism requiring any level of medical attention
    AND
  • Patient does not have more than two α-globin gene deletions
  • AND
  • Patient has obtained a negative test result for all of the following prior to cell collection:
    • Hepatitis B virus (HBV)
    • Hepatitis C virus (HCV)
    • Human immunodeficiency virus (HIV)
    AND
  • Patient is able to provide an adequate number of cells to meet the minimum recommended dose of 3 x 10^6 CD34+ cells/kg
  • AND
  • Patient will receive both of the following:
    • Full myeloablative conditioning with busulfan prior to treatment with Lyfgenia
    • AND
    • Anti-seizure prophylaxis with agents other than phenytoin prior to initiating busulfan conditioning
    AND
  • Prescriber attests that patient will discontinue disease modifying therapies for sickle cell disease (e.g., hydroxyurea, crizanlizumab, voxelotor) 8 weeks before the planned start of mobilization and conditioning
  • AND
  • Prescribed by a provider at a SCD treatment center with expertise in gene therapy
  • AND
  • Prescribed by one of the following:
    • Hematologist/oncologist
    • Specialist with expertise in the diagnosis and management of sickle cell disease
    AND
  • Both of the following:
    • Patient has never received any previous sickle cell gene therapy treatment in their lifetime (i.e., Casgevy, Lyfgenia)
    • Patient has never received prior allogeneic transplant
P & T Revisions

2024-02-15

  1. Lyfgenia Prescribing Information. Bluebird Bio, Inc. Somerville, MA. December 2023.
  2. Exa-Cel and Lovo-Cel: Final Policy Recommendations Policy Recommendations. https://icer.org/wp-content/uploads/2023/08/ICER_Sickle-Cell-Disease_Final-Policy-Recommendations.pdf

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