Adakveo (crizanlizumab) is considered medically necessary for patients 16 years
of age and older who meet the following criteria:
1)
Diagnosis of sickle cell
disease (SCD) with one of the following genotypes:
a.
Homzygous hemoblogin S;
b.
Hemoglobin Sβo-thalassemia;
c.
Hemoglobin Sβ+-thalassemia;
d.
Hemoglobin SC;
2)
Prescribed by or in
consultation with a hematologist;
3)
Hb level > 4g/dL;
4)
Member meets one of the
following:
a.
Member has experienced at
least 2 vasocclusive crises (VOC) within the past 6 months while on hydroxyurea
at up to maximally indicateddoses;
b.
Member has intolerance*
or contraindication to hydroxyurea and has experienced at least 2 VOC within the
past 12 months;
*Myelosuppression and hydroxyurea treatment failure: Myelosuppression is
does-dependent and reversible and does not qualify as treatment failure. NIH
guidelines recommend a 6 month trial on the maximum tolerated dose prior to
considering discontinuation due to treatment failure, whether due to lack of
adherence or failure to respond to therapy. A lack of increase in mean
corpuscular volume (MCV) and/or fetal hemoglobin (HbF) levels is not indication
to discontinue therapy.
5)
Documentation of baseline
incidence of VOC over the last 12 months;
6)
Adakveo is prescribed
concurrently with hydroxyurea, unless contraindicated or clinically significant
adverse effects are experienced;
7)
Adakveo is not prescribed
concurrently with Oxbryta
Reauthorization Criteria:
1)
Member is responding
positively to therapy as evidenced by a documented improvement in the incidence
of VOC from baseline AND
2)
Adakveois prescribed
concurrently with hydroxyurea, unless contraindicated or clinically significant
adverse effects are experienced AND
3)
Adakveo is not prescribed
concurrently with Oxbryta.
Codes
Used In This BI:
1)
J0791 - Injection,
crizanlizumab-tmca, 5mg