Leveraging Molecular and Immune-Based Therapies in Leptomeningeal Metastases

被引:11
|
作者
Wilcox, Jessica A. [1 ]
Boire, Adrienne A. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Neurol, 1275 York Ave, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Brain Tumor Ctr, Human Oncol & Pathogenesis Program, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
CELL LUNG-CANCER; CENTRAL-NERVOUS-SYSTEM; GROWTH-FACTOR RECEPTOR; HER2-POSITIVE BREAST-CANCER; MULTICENTER PHASE-II; LAPATINIB PLUS CAPECITABINE; TRASTUZUMAB EMTANSINE T-DM1; BLOOD-BRAIN-BARRIER; NON-CNS PROGRESSION; CEREBROSPINAL-FLUID;
D O I
10.1007/s40263-022-00975-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Leptomeningeal metastases represent an aggressive stage of cancer with few durable treatment options. Improved understanding of cancer biology, neoplastic reliance on oncogenic driver mutations, and complex immune system interactions have resulted in an explosion in cancer-directed therapy in the last two decades to include small molecule inhibitors and immune checkpoint inhibitors. Most of these therapeutics are underexplored in patients with leptomeningeal metastases, limiting extrapolation of extracranial and even intracranial efficacy outcomes to the unique leptomeningeal space. Further confounding our interpretation of drug activity in the leptomeninges is an incomplete understanding of drug penetration through the blood-cerebrospinal fluid barrier of the choroid plexus. Nevertheless, a number of retrospective studies and promising prospective trials provide evidence of leptomeningeal activity of several small molecule and immune checkpoint inhibitors and underscore potential areas of further therapeutic development for patients harboring leptomeningeal disease.
引用
收藏
页码:45 / 67
页数:23
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