Targeted therapy of brain metastases: latest evidence and clinical implications
- PMID: 29449898
- PMCID: PMC5808839
- DOI: 10.1177/1758834017736252
Targeted therapy of brain metastases: latest evidence and clinical implications
Abstract
Brain metastases (BM) occur in 20-40% of patients with cancer and 60-75% of patients with BM become symptomatic. Due to an aging population and advances in the treatment of primary cancers, patients are living longer and are more likely to experience complications from BM. The diagnosis of BM drastically worsens long-term survival rates, with multiple metastases being a poor prognostic factor. Until recently, the mainstay of treatment consisted of stereotactic radiosurgery (SRS), surgical resection, whole brain radiation therapy (WBRT), or a combination of these modalities. Systemic chemotherapy has been felt largely ineffective in the treatment of BM due to the presence of the blood-brain barrier (BBB), which includes efflux pumps on brain capillaries. Over the past decade however, researchers have identified therapeutic agents that are able to cross the BBB. These findings could make a multimodality treatment approach possible, consisting of surgery, radiation, immunotherapy, and targeted therapy, which could lead to better disease control in this patient population and prolong survival. In this review, we discuss present evidence on available targeted therapies and their role in the treatment of BM from primary tumors with the highest prevalence of central nervous system (CNS) involvement, specifically non-small cell lung cancer (NSCLC), breast cancer melanoma, and renal cell carcinoma.
Keywords: brain metastases; targeted therapy.
Conflict of interest statement
Conflict of interest statement: The authors declare the following potential conflict of interest: Dr. Di Lorenzo has no financial interests or potential conflicts. Dr. Ahluwalia reports grants and personal fees from Monteris Medical, grants and personal fees from Abbvie, grants and personal fees from BMS, grants and personal fees from Astrazeneca, personal fees from Datar Genetics, personal fees from CBT Pharmaceuticals, personal fees from Kadmon Pharmaceuticals, personal fees from Elsevier, grants and personal fees from Novocure, grants from Novartis, grants and personal fees from Incyte, grants from Pharmacyclics, grants from Tracon Pharmaceuticals, personal fees from Prime Oncology, personal fees from Caris Lifesciences, outside the submitted work.
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