Highmark Commercial Medical Policy - Pennsylvania |
Medical Policy: | I-34-011 |
Topic: | Ipilimumab (Yervoy) |
Section: | Injections |
Effective Date: | July 2, 2018 |
Issue Date: | July 2, 2018 |
Last Reviewed: | February 2018 |
Ipilimumab (Yervoy®) is a recombinant, human monoclonal antibody that binds to cytotoxic T-lymphocyte antigen-4 (CTLA-4) and blocks the interaction of CTLA-4 with its ligands CD80/CD86. Blockade of CTLA-4 augments T cell activation and proliferation, resulting in an increase in antitumor responsiveness and allowing the body's immune system to recognize, target, and attack cells in tumors. |
This policy is designed to address medical guidelines that are appropriate for the majority of individuals with a particular disease, illness, or condition. Each person's unique clinical circumstances may warrant individual consideration, based on review of applicable medical records.
Policy Position Coverage is subject to the specific terms of the member’s benefit plan. |
Ipilimumab (Yervoy) may be considered medically necessary in individuals 12 years of age or older when ANY ONE of the following indications is met:
Central Nervous System Cancers - Limited (one to three) Metastatic Lesions
Central Nervous System Cancers - Multiple (greater than three) Metastatic Lesions
Melanoma
Uveal Melanoma
Small Cell Lung Cancer (SCLC)
Malignant Pleural Mesothelioma
The use of ipilimumab (Yervoy) for any other indication is considered experimental/investigational. Scientific evidence does not support the use of ipilimumab (Yervoy) for any other indication.
NOTE: Dosage recommendations per the FDA label. Refer to medical policy I-120 for information on nivolumab (Opdivo)/ipilimumab (Yervoy) combination therapy. |
Place of Service: Outpatient |
The administration of Ipilimumab (Yervoy) is typically an outpatient procedure which is only eligible for coverage as an inpatient procedure in special circumstances, including, but not limited to, the presence of a co-morbid condition that would require monitoring in a more controlled environment such as the inpatient setting.
The policy position applies to all commercial lines of business |
Denial Statements |
Services that do not meet the criteria of this policy will be considered experimental/investigational (E/I). A network provider can bill the member for the experimental/investigational service. The provider must give advance written notice informing the member that the service has been deemed E/I. The member must be provided with an estimate of the cost and the member must agree in writing to assume financial responsibility in advance of receiving the service. The signed agreement must be maintained in the provider’s records.
Links |
03/2017, Criteria Revised for Ipilimumab (Yervoy®)
04/2018, Coverage Guidelines Revised for Ipilimumab (Yervoy®)