Gleevec — 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