Lutathera (lutetium Lu 177 dotatate) is considered medically necessary for
members meeting the following criteria:
1)
Neuroendocrine Tumors
(must meet all):
a.
Diagnosis of a
somatostatin receptor-positive NET of one of the following origins (i or ii):
i.
Gastrointestinal tract or
pancreas;
ii.
Lung or thymus
(off-label)
b.
Prescribed by or in
consultation with an oncologist;
c.
Age > 18 years of
age;
d.
Disease is metastatic or
locally advanced, and unresectable;
e.
Member experienced
disease progression while on a long-acting somatostatin analog (e.g. octreotide,
lanreotide);
f.
Dose does not exceed
7.4GBq (200mCi) every 8 weeks, up to a total of 4 doses.
Approval duration: 32
weeks (no more than 4 total doses)
2)
Pheochromocytoma/Paraganglioma (off-label) (must meet all):
a.
Diagnosis of somatostatin
receptor-positive pheochromocytoma/paraganglioma;
b.
Prescribed by or in
consultation with an oncologist;
c.
Disease is metastatic or
locally advanced, and unresectable;
d.
Dose does not exceed
7.4GBq (200 mCi) every 8 weeks, up to a total of 4 doses.
Approval
duration: 32 weeks (no more than 4 total doses).
Codes
Used In This BI:
A9513 – Lutetium Lu 177, dotatate, therapeutic, 1 millicurie