Cyramza is considered medically necessary for members who meet the following
criteria:
1)
Member has a diagnosis of
advanced gastric cancer or gastro-esophageal junction adenocarcinoma
AND
2)
Member had disease
progression or intolerance to a prior chemotherapy regimen containing a
fluoropyrimidine- or platinum-agent
OR
3)
Member has diagnosis of
metastatic colorectal cancer AND
4)
Member has experienced
disease progression on or after prior therapy with bevacizumab, oxaliplatin, and
a fluoropyrimidine, in combination with irinotecan, folinic acid (leucovorin),
and 5-fluourouracil.
OR
5)
Member has a diagnosis of
metastatic non-small cell lung cancer (NSCLC) AND
6)
Will be used in
combination with docetaxel AND
7)
Has experience disease
progression on or after platinum-based chemotherapy
OR
8) Member has
diagnosis of progressive hepatocellular carcinoma (HCC) AND
9) AFP >
400ng/mL AND
10) Disease has
progressed on or after therapy with Nexavar
Reauthorization (after 12 months) will be provided for members who have not
experienced any of the following:
1)
Severe bleeding
2)
Grade 3 or 4
infusion-related reactions
3)
Severe hypertension that
cannot be controlled with optimized antihypertensive therapy
4)
Urine protein level >3
g/24 hours or in the setting of nephrotic syndrome
5)
Arterial Thrombolic
events
6)
Gastrointestinal
perforation
Codes
Used In This BI:
J9308 – Injection, Ramucirumab, 5mg (Cyramza)