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deferasiroxCareFirst (Caremark)

Chronic iron overload in patients with non-transfusion-dependent thalassemia (NTDT) syndromes

Initial criteria

  • Member meets any of the following: Pretreatment serum ferritin level ≥ 800 mcg/L; OR Pretreatment liver iron concentration (LIC) ≥ 5 mg Fe/g dw; OR Pretreatment serum ferritin level > 300 mcg/L to < 800 mcg/L with clinical or laboratory measures indicative of iron overload (e.g., liver disease, renal disease)
  • Dose of deferasirox tablet for suspension/Exjade will not exceed 20 mg/kg per day
  • Dose of deferasirox/Jadenu will not exceed 14 mg/kg per day

Reauthorization criteria

  • Member is experiencing benefit from therapy as evidenced by a decrease in serum ferritin levels as compared to pretreatment baseline
  • Serum ferritin level is not consistently below 300 mcg/L

Approval duration

6 months