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Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)

机译:黑色素瘤的透视:黑素瘤大桥的会议报告(2017年11月30日,2017年12月30日,那不勒斯,意大利)

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摘要

Abstract Metastatic melanoma represents a challenging clinical situation and, until relatively recently, there was an absence of effective treatment options. However, in 2011, the advanced melanoma treatment landscape was revolutionised with the approval of the anti-cytotoxic T-lymphocyte-associated protein-4 checkpoint inhibitor ipilimumab and the selective BRAF kinase inhibitor vemurafenib, both of which significantly improved overall survival. Since then, availability of new immunotherapies, especially the anti-programmed death-1 checkpoint inhibitors, as well as other targeted therapies, have further improved outcomes for patients with advanced melanoma. Seven years on from the first approval of these novel therapies, evidence for the use of various immune-based and targeted approaches is continuing to increase at a rapid rate. Improved understanding of the tumour microenvironment and tumour immuno-evasion strategies has resulted in different approaches to target and harness the immune response. These new immune-based approaches offer the opportunity for various approaches with distinct modes of action being used in combination with one another, as well as combined with other treatment modalities such as targeted therapy, electrochemotherapy and surgery. The increasing number of treatment options that are now available has resulted in a growing need to identify which patients will derive most benefit from which treatments. Much research is now focused on the identification of biomarkers that can be utilised to help select patients for treatment. These and other recent advances in the management of melanoma were the focus of discussions at the third Melanoma Bridge meeting (30 November–2 December, 2017, Naples, Italy), which is summarised in this report.
机译:摘要转移性黑色素瘤代表着挑战性的临床情况,直到相对最近,没有有效的治疗方案。然而,在2011年,通过抗细胞毒性T淋巴细胞相关蛋白-4检查点抑制剂IPILIMIMAB和选择性BRAF激酶抑制剂vemureafenib的批准,彻底改变了先进的黑色素瘤治疗景观,这两者都显着提高了整体存活率。从那时起,新免疫疗法的可用性,特别是反编程死亡-1检查点抑制剂以及其他有针对性的疗法,对先进黑素瘤的患者进一步改善了结果。从第一次批准这些小说疗法的七年,使用各种免疫和有针对性方法的证据继续以迅速的速度增加。改善对肿瘤微环境和肿瘤免疫逃号策略的理解导致了不同的靶向和束缚免疫应答的方法。这些新的基于免疫力的方法提供了各种方法的机会,具有不同的行动模式,以及与其他治疗,电化学疗法和手术等其他治疗方式结合使用。现在可用的治疗方面的越来越多的治疗方案导致了越来越需要确定哪些患者将从哪些治疗中获得哪些患者。现在研究了很多研究识别可用于帮助选择患者治疗的生物标志物。 Melanoma的管理的这些和其他最新进展是第三黑色素瘤桥梁会议讨论的重点(2017年11月30日,意大利,意大利十二月二十日),这在本报告中总结道。

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