I.
Initial Approval Criteria
Alzheimer’s Disease
(must meet all):
A. Diagnosis of MCI or
mild AD dementia;
B. Prescribed by or in
consultation with a geriatrician or neurologist;
C. Age >50 and
<90 years;
D. Documentation of the
presence of beta-amyloid plaques verified by one of the following (1 or 2):
1. Positron emission
tomography scan;
2. Cerebrospinal fluid
testing;
E. Documentation of one
of the following baseline cognitive tests (1 or 2):
1.
Mini-Mental State Examination (MMSE) score > 22;
2.
Montreal Cognitive Assessment (MoCA) score > 16;
F. Documentation of one
of the following baseline functional tests and the resulting score (1, 2, or 3):
1. Functional Assessment Questionnaire (FAQ) score <
9;
2.
Functional Assessment Staging Test (FAST) score of 3-4;
3.
Clinical Dementia Rating-Sum of Boxes (CDR-SB) of 0.5-9;
G. Documentation of
recent (within the last year) brain magnetic resonance imaging (MRI)
demonstrating all of the following (1-4):
1. Fewer than 4
microhemorrhages (defined as < 10mm at the greatest diameter);
2.
Absence of any macrohemorrhages > 10mm at greatest diameter;
3.
Absence of superficial siderosis;
4. Absence of vasogenic
edema, cerebral contusion, encephalomalacia, aneurysms, or vascular
malformations;
H. Prescriber attestation
that the prescriber has discussed with the member the potentially increased risk
of amyloid-related imaging abnormalities (ARIA) in those who are ApoE4 genetic
homozygotes and in those who are currently taking, or who may eventually need,
concomitant anticoagulant or antithrombotic therapy;
I.
Member has no history of
transient ischemic attacks (TIA), stroke, or seizures within the past 12 months;
J. Dose does not exceed
10mg/kg every 2 weeks
Approval Duration: 3 months (6 doses of infusion
only)
II.
Continued Therapy
A. Alzheimer’s Disease
(must meet
all):
1. Member is responding
positively to therapy as evidenced by slowed decline in cognition;
2. Documentation of one
of the following baseline cognitive tests (a or b):\
a. Mini-Mental State Examination (MMSE) score >22;
b. Montreal Cognitive Assessment (MoCA) score > 16;
3. Documentation of one
of the following baseline functional tests and the resulting score (a, b, or c):
a. Functional Assessment Questionnaire (FAQ) score < 9;
b. Functional Assessment Staging Test (FAST) score of 3-4;
c. Clinical Dementia Rating-Sum of Boxes (CDR-SB) of 0.5-9;
4. Prior to the 7th
and 14th infusions, documentation of a recent (within the last month)
brain MRI showing all of the following (a, b, and c):
a. Absence of any
microhemorrhage (> 10mm at greatest diameter; symptomatic or not);
b.
Fewer than 10 cerebral microhemorrhages cumulatively (symptomatic or not);
c. Absence of symptomatic cerebral microhemorrhages or symptomatic
superficial siderosis;
5. If request is for a
dose increase, new dose does not exceed 10mg/kg once very 2 weeks.
Approval duration:
·
Members with < 7 total
infusions: up to the 6th total infusion
·
Member with < 14 total
infusions but > 7 total infusions: up to the 13th total infusion
·
Member with > 14
total infusions: 12 infusions per PA approval
Codes
Used In This BI:
1)
J0174 – Injection,
lecanemab-irmb, 1mg