Systemic therapy of brain metastases: non-small cell lung cancer, breast cancer, and melanoma

被引:2
|
作者
Chamberlain, Marc C. [1 ,3 ,4 ]
Baik, Christina S. [1 ,2 ,5 ]
Gadi, Vijayakrishna K. [1 ,2 ,5 ]
Bhatia, Shailender [1 ,5 ]
Chow, Laura Q. M. [1 ,2 ,5 ]
机构
[1] Seattle Canc Ctr Alliance, 825 Eastlake Ave East,Box 358081,G6-800, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA
[3] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Neurol Surg, Seattle, WA 98195 USA
[5] Univ Washington, Div Med Oncol, Seattle, WA 98195 USA
关键词
Brain metastases; breast cancer; blood-brain barrier; melanoma; non-small cell lung cancer; CENTRAL-NERVOUS-SYSTEM; PHASE-II TRIAL; LAPATINIB PLUS CAPECITABINE; P-GLYCOPROTEIN ABCB1; TYROSINE KINASE INHIBITORS; RESISTANCE PROTEIN ABCG2; CEREBROSPINAL-FLUID CONCENTRATIONS; DISSEMINATED MALIGNANT-MELANOMA; ALBUMIN-BOUND PACLITAXEL; OPEN-LABEL;
D O I
10.1093/neuonc/now197
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Brain metastases (BM) occur frequently in many cancers, particularly non-small cell lung cancer (NSCLC), breast cancer, and melanoma. The development of BM is associated with poor prognosis and has an adverse impact on survival and quality of life. Commonly used therapies for BM such as surgery or radiotherapy are associated with only modest benefits. However, recent advances in systemic therapy of many cancers have generated considerable interest in exploration of those therapies for treatment of intracranial metastases. This review discusses the epidemiology of BM from the aforementioned primary tumors and the challenges of using systemic therapies for metastatic disease located within the central nervous system. Cumulative data from several retrospective and small prospective studies suggest that molecularly targeted systemic therapies may be an effective option for the treatment of BM from NSCLC, breast cancer, and melanoma, either as monotherapy or in conjunction with other therapies. Larger prospective studies are warranted to further characterize the efficacy and safety profiles of these targeted agents for the treatment of BM.
引用
收藏
页码:I1 / I24
页数:24
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