Highmark Commercial Medical Policy - Pennsylvania |
Medical Policy: | I-65-002 |
Topic: | Paclitaxel, albumin-bound (Abraxane ®) |
Section: | Injections |
Effective Date: | May 30, 2016 |
Issue Date: | May 30, 2016 |
Last Reviewed: | March 2016 |
Paclitaxel, albumin-bound (Abraxane) is an antimicrotubule agent that promotes the assembly of microtubules from tubulin dimers and stabilizes microtubules by preventing depolymerization. This stability results in the inhibition of the normal dynamic reorganization of the microtubule network that is essential for vital interphase and mitotic cellular functions. Abraxane is an albumin-bound form of paclitaxel, a natural product with antitumor activity. In contrast to solvent-based paclitaxel, which requires premedication to decrease the risks of hypersensitivity reactions (eg, difficulty breathing, hives, swollen eyes and lips), Abraxane requires no premedication. |
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. |
Paclitaxel, albumin-bound (Abraxane ®) may be considered medically necessary when used in the treatment of ANY ONE the following condition(s):
Breast Cancer - Invasive
Breast Cancer (metastatic)
Cervical Cancer
Melanoma
Non-small Cell Lung Cancer (NSCLC)
Ovarian Cancer – Epithelial Ovarian Cancer/Fallopian Tube Cancer/Primary Peritoneal Cancer
Pancreatic Adenocarcinoma Cancer
The use of paclitaxel, albumin-bound (Abraxane) for all other indications is considered experimental/investigational, and therefore, non-covered. Peer reviewed literature does not support the use of paclitaxel, albumin-bound (Abraxane) for any indications other than those listed on this medical policy.
FEP Guidelines |
Under the Federal Employees Program, all services that utilize FDA-approved drugs, devices, or biological products are eligible when intended for the treatment of a serious life-threatening condition and when medically necessary and appropriate for the patient’s condition. |
Dosage recommendations per the FDA label. |
Place of Service: Outpatient |
Experimental/Investigational (E/I) services are not covered regardless of place of service.
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 |
01/2015, Clinical Criteria Established For Paclitaxel, Albumin-Bound (Abraxane)
03/2016, Clinical Criteria Revised For Paclitaxel, Albumin-Bound (Abraxane)