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晚期黑色素瘤靶向治疗和免疫治疗的皮肤副作用

Cutaneous Side Effects of Targeted Therapy and Immunotherapy for Advanced Melanoma.

作者信息

Russo Irene, Zorzetto Ludovica, Chiarion Sileni Vanna, Alaibac Mauro

机构信息

Unit of Dermatology, University of Padua, Via Gallucci 4, 35128 Padova, Italy.

Istituto Oncologico Veneto I.R.C.C.S., Via Gattamelata 64, 35128 Padova, Italy.

出版信息

Scientifica (Cairo). 2018 Dec 30;2018:5036213. doi: 10.1155/2018/5036213. eCollection 2018.

DOI:10.1155/2018/5036213
PMID:30693134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6332919/
Abstract

Melanoma is one of the most fatal cancers, and its incidence is increasing worldwide. Thanks to the better understanding of the molecular mechanisms involved in the pathogenesis of melanoma, recently new targeted agents have been developed. In this article, we review the current state of knowledge of clinical presentation, mechanisms, and management of the most common cutaneous side effects observed during treatment with targeted and immunological therapies approved for advanced melanoma. We include discussion of BRAF/MEK inhibitors and immune-checkpoint inhibitors, notably CTLA-4 and PD-1 inhibitors.

摘要

黑色素瘤是最致命的癌症之一,其发病率在全球范围内呈上升趋势。由于对黑色素瘤发病机制中涉及的分子机制有了更深入的了解,最近已开发出新型靶向药物。在本文中,我们综述了在晚期黑色素瘤获批的靶向治疗和免疫治疗期间观察到的最常见皮肤副作用的临床表现、机制及管理方面的当前知识状况。我们讨论了BRAF/MEK抑制剂和免疫检查点抑制剂,尤其是CTLA-4和PD-1抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5d8/6332919/fe658b1b5295/SCIENTIFICA2018-5036213.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5d8/6332919/4c6d05cf75bd/SCIENTIFICA2018-5036213.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5d8/6332919/fe658b1b5295/SCIENTIFICA2018-5036213.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5d8/6332919/4c6d05cf75bd/SCIENTIFICA2018-5036213.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5d8/6332919/fe658b1b5295/SCIENTIFICA2018-5036213.002.jpg

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J Skin Cancer. 2018 Jan 21;2018:9602540. doi: 10.1155/2018/9602540. eCollection 2018.
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Encorafenib plus binimetinib versus vemurafenib or encorafenib in patients with BRAF-mutant melanoma (COLUMBUS): a multicentre, open-label, randomised phase 3 trial.
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