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Unless otherwise noted, the following pharmacy (drugs & biologics) coverage policies were modified effective February 15, 2017: |
| Unassigned Drug or Biologic Code Medical Precertification – (1701) |
New |
- Supports unassigned medical codes impacting EviCore Oncology management process, as well as potential expansion to support unassigned (non-J9999) code precertification.
- Added Sustol (granisetron extended-release) criteria.
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| Denosumab (Prolia® and Xgeva®) - (1212) |
Modified |
- Important changes in coverage criteria:
- Expanded diagnosis criteria for osteoporosis to align with American Association of Clinical Endocrinologists (AACE) and American College of Endocrinology (ACE) 2016 updated guidelines.
- Updated criteria for Prolia in prostate cancer and Xgeva to align with recommendations from National Comprehensive Cancer Network (NCCN) guidelines.
- Added criteria for Prolia and breast cancer that individual is at high risk for fractures.
- Added criteria for Xgeva and Prolia in breast cancer:
- No pre-existing hypocalcemia for all covered uses.
- Individual is not pregnant.
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| Erythropoiesis Stimulating Agents (ESA) - (5016) |
Modified |
- Important changes in coverage criteria:
- Added criteria for anemia associated with myelofibrosis for darbepoetin alfa and epoetin alfa.
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| Implantable Hormone Pellets - (1504) |
Modified |
- Important changes in coverage criteria:
- Expanded diagnosis criteria for:
- hypogonadism,
- hypogonadotropic hypogonadism,
- delayed puberty.
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| Interferon Therapy - (1315) |
Modified |
- Important changes in coverage criteria:
- Reincorporated the FDA-approved condylomata acuminata indication to Intron A.
- Added standard sample product note per coverage policy template.
- Added Hepatitis E and Middle East respiratory syndrome to the experimental, investigational, or unproven (EIU) list.
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| Modafinil/Armodafinil (Provigil®/Nuvigil®) - (1501) |
Modified |
- Important changes in coverage criteria:
- Added criteria for Individual and Family Plans to include a trial of generic versions of both products before approval of either brand name product.
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| Step Therapy – (1109) |
Modified |
- Important changes in coverage criteria:
- Added gabapentin (Neurontin®) and Lyrica® (pregabalin) as step 1 agents in the Horizant B / Emerging Step Therapy to account for Horizant’s postherpetic neuralgia FDA-approved indication.
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| Testosterone undecanoate (Aveed®) - (1503) |
Modified |
- Important changes in coverage criteria:
- Added appropriateness of use criteria for hypogonadism and hypogonadotropic hypogonadism by adding:
- Documentation of signs and symptoms of androgen deficiency.
- Two early morning, low total serum testosterone levels (below the testing laboratory's normal reference range) drawn on different days.
- Removed criteria requiring failure, contraindication, or intolerance to a three-month trial of topical or generic injectable testosterone therapy.
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| Glucarpidase (Voraxaze®) - (1302) |
Retired |
- HCPCS code for glucarpidase moved to fast-certification status/no precertification required.
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| Radium Ra-223 dichloride (Xofigo®) - (1404) |
Retired |
- HCPCS code will be managed through EviCore Radiation Oncology guideline/program management criteria.
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