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乳腺癌脑及软脑膜转移的治疗。

Management of Brain and Leptomeningeal Metastases from Breast Cancer.

机构信息

Department of Neuro-Oncology, University and City of Health and Science Hospital, 10126 Turin, Italy.

Department of Biomedical Sciences and Human Oncology, University of Bari Aldo Moro, 70121 Bari, Italy.

出版信息

Int J Mol Sci. 2020 Nov 12;21(22):8534. doi: 10.3390/ijms21228534.

Abstract

The management of breast cancer (BC) has rapidly evolved in the last 20 years. The improvement of systemic therapy allows a remarkable control of extracranial disease. However, brain (BM) and leptomeningeal metastases (LM) are frequent complications of advanced BC and represent a challenging issue for clinicians. Some prognostic scales designed for metastatic BC have been employed to select fit patients for adequate therapy and enrollment in clinical trials. Different systemic drugs, such as targeted therapies with either monoclonal antibodies or small tyrosine kinase molecules, or modified chemotherapeutic agents are under investigation. Major aims are to improve the penetration of active drugs through the blood-brain barrier (BBB) or brain-tumor barrier (BTB), and establish the best sequence and timing of radiotherapy and systemic therapy to avoid neurocognitive impairment. Moreover, pharmacologic prevention is a new concept driven by the efficacy of targeted agents on macrometastases from specific molecular subgroups. This review aims to provide an overview of the clinical and molecular factors involved in the selection of patients for local and/or systemic therapy, as well as the results of clinical trials on advanced BC. Moreover, insight on promising therapeutic options and potential directions of future therapeutic targets against BBB and microenvironment are discussed.

摘要

在过去的 20 年中,乳腺癌(BC)的管理迅速发展。系统治疗的改善使颅外疾病得到了显著控制。然而,脑(BM)和软脑膜转移(LM)是晚期 BC 的常见并发症,也是临床医生面临的挑战。一些为转移性 BC 设计的预后评分用于选择合适的患者进行适当的治疗和临床试验入组。不同的系统药物,如针对单克隆抗体或小分子酪氨酸激酶的靶向治疗药物,或改良的化疗药物正在研究中。主要目标是提高活性药物通过血脑屏障(BBB)或脑肿瘤屏障(BTB)的穿透率,并确定放疗和系统治疗的最佳顺序和时机,以避免神经认知障碍。此外,药物预防是一个新的概念,其驱动力是针对特定分子亚组的大转移灶的靶向药物的疗效。本文旨在概述局部和/或系统治疗患者选择中涉及的临床和分子因素,以及晚期 BC 临床试验的结果。此外,还讨论了针对 BBB 和微环境的有前途的治疗选择和潜在治疗靶点的方向。

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