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黑色素瘤脑转移:CTLA-4 抗体治疗的临床活性。

Brain metastasis in melanoma: clinical activity of CTLA-4 antibody therapy.

机构信息

Medical Oncology, University of Washington, Seattle Cancer Care Alliance, Seattle, WA 98109-1023, USA.

出版信息

Semin Oncol. 2010 Oct;37(5):468-72. doi: 10.1053/j.seminoncol.2010.09.014.

Abstract

Melanoma metastasizes frequently to the brain, and brain metastases generally drive the prognosis of melanoma patients. Surgical and radiation therapy improve the outcome of selected melanoma patients with brain metastasis, while systemic treatment using cytotoxic agents still plays a limited role. Temozolomide and fotemustine are preferentially used in melanoma patients with brain metastases in the United States and in Europe, respectively, with modest clinical activity. However, the results obtained with either agent are still limited, and efforts are needed to improve the outcome of these patients who are generally excluded from clinical trials. Among therapeutic agents in development, antibodies that block the interaction of cytotoxic T-lymphocyte-associated antigen (CTLA-4) with its ligands B7.1 and B7.2 and thus enhance antitumor immune responses have shown clinical benefit in patients with metastatic melanoma, including durable control of brain metastases. This chapter reviews the current data and the rationale for ongoing and future trials of combination cytotoxic plus immunomodulatory therapy by US and Italian multicenter trial groups.

摘要

黑色素瘤经常转移到大脑,脑转移通常会影响黑色素瘤患者的预后。手术和放疗改善了选择的有脑转移的黑色素瘤患者的结果,而使用细胞毒性药物的全身治疗仍然作用有限。替莫唑胺和福莫司汀分别是美国和欧洲黑色素瘤脑转移患者的首选药物,具有适度的临床活性。然而,这两种药物的结果仍然有限,需要努力改善这些通常被排除在临床试验之外的患者的结果。在开发中的治疗药物中,阻断细胞毒性 T 淋巴细胞相关抗原 (CTLA-4)与其配体 B7.1 和 B7.2 相互作用从而增强抗肿瘤免疫反应的抗体,在转移性黑色素瘤患者中显示出临床获益,包括对脑转移的持久控制。本章综述了美国和意大利多中心试验组正在进行和未来联合细胞毒性加免疫调节治疗的临床试验数据和原理。

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