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BRAF+MEK抑制的免疫效应。

Immunological effects of BRAF+MEK inhibition.

作者信息

Ascierto Paolo A, Dummer Reinhard

机构信息

Unit of Melanoma, Cancer Immunotherapy and Development Therapeutics, Istituto Nazionale Tumori - IRCCS Fondazione "G. Pascale", Napoli, Italy.

Department of Dermatology, University Hospital Zürich Skin Cancer Center, Zürich, Switzerland.

出版信息

Oncoimmunology. 2018 Jul 23;7(9):e1468955. doi: 10.1080/2162402X.2018.1468955. eCollection 2018.

Abstract

Recent developments in immunotherapy have prolonged overall survival in metastatic melanoma with the possibility to reach a long-term benefit. Targeted therapies based on BRAF and MEK inhibition also seem to have a long-term beneficial effect, which is more evident in patients with favorable baseline characteristics, namely normal levels of lactate dehydrogenase, without brain metastases, and low tumor burden. This long-term benefit of targeted therapies might be related to an immune-modulation: indeed BRAF and MEK inhibitors affect tumor microenvironment and immune surveillance, and it has been shown that patients with complete response to targeted treatment have a pre-existing favorable immunologic signature.

摘要

免疫疗法的最新进展延长了转移性黑色素瘤患者的总生存期,并有可能带来长期益处。基于BRAF和MEK抑制的靶向治疗似乎也具有长期有益效果,这在具有良好基线特征的患者中更为明显,即乳酸脱氢酶水平正常、无脑转移且肿瘤负荷低的患者。靶向治疗的这种长期益处可能与免疫调节有关:事实上,BRAF和MEK抑制剂会影响肿瘤微环境和免疫监视,并且已经表明,对靶向治疗完全缓解的患者具有预先存在的良好免疫特征。

相似文献

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Immunological effects of BRAF+MEK inhibition.BRAF+MEK抑制的免疫效应。
Oncoimmunology. 2018 Jul 23;7(9):e1468955. doi: 10.1080/2162402X.2018.1468955. eCollection 2018.

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Targeted therapies induced depigmentation: a review.靶向治疗引起的色素脱失:综述
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MEK inhibition and immune responses in advanced melanoma.晚期黑色素瘤中的MEK抑制与免疫反应
Oncoimmunology. 2017 Aug 10;6(8):e1335843. doi: 10.1080/2162402X.2017.1335843. eCollection 2017.

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