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本文引用的文献

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Phase 1 study of twice weekly pulse dose and daily low-dose erlotinib as initial treatment for patients with EGFR-mutant lung cancers.针对表皮生长因子受体(EGFR)突变型肺癌患者,每周两次脉冲剂量和每日低剂量厄洛替尼作为初始治疗的1期研究。
Ann Oncol. 2017 Feb 1;28(2):278-284. doi: 10.1093/annonc/mdw556.
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Pembrolizumab in Patients With Advanced Triple-Negative Breast Cancer: Phase Ib KEYNOTE-012 Study.帕博利珠单抗治疗晚期三阴性乳腺癌患者:Ib期KEYNOTE-012研究
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Activity and safety of ceritinib in patients with ALK-rearranged non-small-cell lung cancer (ASCEND-1): updated results from the multicentre, open-label, phase 1 trial.色瑞替尼在间变性淋巴瘤激酶(ALK)重排的非小细胞肺癌患者中的活性与安全性(ASCEND-1):多中心、开放标签、1期试验的更新结果
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Translational Breast Cancer Research Consortium (TBCRC) 022: A Phase II Trial of Neratinib for Patients With Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer and Brain Metastases.转化型乳腺癌研究联盟(TBCRC)022 研究:曲妥珠单抗耐药的 HER2 阳性乳腺癌脑转移患者接受奈拉替尼治疗的 II 期临床试验。
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MET Exon 14 Mutations in Non-Small-Cell Lung Cancer Are Associated With Advanced Age and Stage-Dependent MET Genomic Amplification and c-Met Overexpression.非小细胞肺癌中的 MET 外显子 14 突变与高龄和与 MET 基因扩增和 c-Met 过表达相关的疾病进展程度有关。
J Clin Oncol. 2016 Mar 1;34(7):721-30. doi: 10.1200/JCO.2015.63.4600. Epub 2016 Jan 4.
6
Alectinib in Crizotinib-Refractory ALK-Rearranged Non-Small-Cell Lung Cancer: A Phase II Global Study.克唑替尼治疗后进展的间变性淋巴瘤激酶阳性非小细胞肺癌患者中阿来替尼的疗效:一项全球 II 期研究。
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Extended Survival and Prognostic Factors for Patients With ALK-Rearranged Non-Small-Cell Lung Cancer and Brain Metastasis.ALK重排的非小细胞肺癌合并脑转移患者的生存延长及预后因素
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Brain accumulation of the EML4-ALK inhibitor ceritinib is restricted by P-glycoprotein (P-GP/ABCB1) and breast cancer resistance protein (BCRP/ABCG2).EML4-ALK抑制剂色瑞替尼在大脑中的蓄积受到P-糖蛋白(P-GP/ABCB1)和乳腺癌耐药蛋白(BCRP/ABCG2)的限制。
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Brain Exposure of Two Selective Dual CDK4 and CDK6 Inhibitors and the Antitumor Activity of CDK4 and CDK6 Inhibition in Combination with Temozolomide in an Intracranial Glioblastoma Xenograft.两种选择性CDK4和CDK6抑制剂在脑内的暴露情况以及CDK4和CDK6抑制与替莫唑胺联合应用于颅内胶质母细胞瘤异种移植模型中的抗肿瘤活性
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脑转移瘤的全身治疗:非小细胞肺癌、乳腺癌和黑色素瘤。

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

作者信息

Chamberlain Marc C, Baik Christina S, Gadi Vijayakrishna K, Bhatia Shailender, Chow Laura Q M

机构信息

Seattle Cancer Center Alliance, Seattle, Washington (M.C.C., C.S.B., V.K.G., S.B., L.Q.M.C.); Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington (C.S.B., V.K.G., L.Q.M.C.); Departments of Neurology and Neurological Surgery, University of Washington, Seattle, Washington (M.C.C.); Division of Medical Oncology, University of Washington, Seattle, Washington (C.S.B., V.K.G., S.B., L.Q.M.C)

Seattle Cancer Center Alliance, Seattle, Washington (M.C.C., C.S.B., V.K.G., S.B., L.Q.M.C.); Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington (C.S.B., V.K.G., L.Q.M.C.); Departments of Neurology and Neurological Surgery, University of Washington, Seattle, Washington (M.C.C.); Division of Medical Oncology, University of Washington, Seattle, Washington (C.S.B., V.K.G., S.B., L.Q.M.C).

出版信息

Neuro Oncol. 2017 Jan;19(1):i1-i24. doi: 10.1093/neuonc/now197.

DOI:10.1093/neuonc/now197
PMID:28031389
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5193029/
Abstract

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.

摘要

脑转移瘤(BM)在许多癌症中频繁发生,尤其是非小细胞肺癌(NSCLC)、乳腺癌和黑色素瘤。脑转移瘤的发生与预后不良相关,对生存和生活质量有不利影响。常用的脑转移瘤治疗方法,如手术或放疗,仅具有适度的益处。然而,许多癌症全身治疗的最新进展引发了对探索这些疗法用于治疗颅内转移瘤的极大兴趣。本综述讨论了上述原发性肿瘤的脑转移瘤流行病学以及使用全身疗法治疗位于中枢神经系统内的转移性疾病所面临的挑战。几项回顾性和小型前瞻性研究的累积数据表明,分子靶向全身疗法可能是治疗非小细胞肺癌、乳腺癌和黑色素瘤脑转移瘤的有效选择,可作为单一疗法或与其他疗法联合使用。有必要进行更大规模的前瞻性研究,以进一步明确这些靶向药物治疗脑转移瘤的疗效和安全性。