Zytiga — Blue Cross Blue Shield of Texas
associated condition related to stage four advanced, metastatic cancer
Preferred products
- everolimus
- imatinib
- gefitinib
- sorafenib tosylate
- dasatinib
- sunitinib
- erlotinib
- bexarotene
- temozolomide
- lapatinib
- pazopanib
- capecitabine
- abiraterone
Initial criteria
- ONE of the following:
- A. BOTH of the following:
- 1. Prescriber states or documents stage four advanced, metastatic cancer and requested agent used to treat it OR associated condition [chart notes required]
- 2. Use consistent with best practices, supported by evidence-based literature, and FDA approved
- B. Patient currently treated and stable on requested agent [chart notes required]
- C. Patient tried and had inadequate response to generic equivalent [chart notes required]
- D. Generic equivalent discontinued due to lack of efficacy, effectiveness, diminished effect, or adverse event [chart notes required]
- E. Patient has intolerance or hypersensitivity to generic equivalent not expected with requested brand [chart notes required]
- F. Patient has FDA labeled contraindication to generic equivalent not expected with requested brand [chart notes required]
- G. Generic equivalent expected to be ineffective OR cause adherence barrier OR worsen comorbidities OR decrease functional ability OR cause harm [chart notes required]
- H. Generic equivalent not in best interest of patient based on medical necessity [chart notes required]
- I. Patient tried another drug in same class or mechanism as generic equivalent discontinued due to lack of efficacy, effectiveness, or adverse event [chart notes required]
- J. Support for use of requested brand over generic equivalent
- Patient does not have any FDA labeled contraindications to requested agent
Approval duration
12 months