Department of Oncology, Lausanne University Hospital, Lausanne, Switzerland; Ludwig Centre and Swiss Institute of Bioinformatics, Génopode, Lausanne, Switzerland.
Department of Dermatology, Medical University Vienna, Austria.
Cancer Treat Rev. 2015 Sep;41(8):660-70. doi: 10.1016/j.ctrv.2015.05.012. Epub 2015 Jun 4.
Before 2011, patients with advanced or metastatic melanoma had a particularly poor long-term prognosis. Since traditional treatments failed to confer a survival benefit, patients were preferentially entered into clinical trials of investigational agents. A greater understanding of the epidemiology and biology of disease has underpinned the development of newer therapies, including six agents that have been approved in the EU, US and/or Japan: a cytotoxic T-lymphocyte antigen-4 inhibitor (ipilimumab), two programmed cell death-1 receptor inhibitors (nivolumab and pembrolizumab), two BRAF inhibitors (vemurafenib and dabrafenib) and a MEK inhibitor (trametinib). The availability of these treatments has greatly improved the outlook for patients with advanced melanoma; however, a major consideration for physicians is now to determine how best to integrate these agents into clinical practice. Therapeutic decisions are complicated by the need to consider patient and disease characteristics, and individual treatment goals, alongside the different efficacy and safety profiles of agents with varying mechanisms of action. Long-term survival, an outcome largely out of reach with traditional systemic therapies, is now a realistic goal, creating the additional need to re-establish how clinical benefit is evaluated. In this review we summarise the current treatment landscape in advanced melanoma and discuss the promise of agents still in development. We also speculate on the future of melanoma treatment and discuss how combination and sequencing approaches may be used to optimise patient care in the future.
在 2011 年之前,晚期或转移性黑色素瘤患者的长期预后特别差。由于传统治疗未能带来生存获益,因此患者优先进入了研究药物的临床试验。对疾病的流行病学和生物学有了更深入的了解,为新疗法的开发奠定了基础,包括在欧盟、美国和/或日本批准的六种药物:细胞毒性 T 淋巴细胞抗原-4 抑制剂(ipilimumab)、两种程序性死亡受体-1 抑制剂(nivolumab 和 pembrolizumab)、两种 BRAF 抑制剂(vemurafenib 和 dabrafenib)和一种 MEK 抑制剂(trametinib)。这些治疗方法的出现极大地改善了晚期黑色素瘤患者的预后;然而,医生现在面临的一个主要问题是如何将这些药物最好地整合到临床实践中。治疗决策的复杂性在于需要考虑患者和疾病特征以及个体治疗目标,同时还需要考虑具有不同作用机制的药物的不同疗效和安全性特征。长期生存是传统系统治疗难以实现的目标,现在已经成为现实,这就需要重新建立如何评估临床获益的方法。在这篇综述中,我们总结了晚期黑色素瘤的当前治疗现状,并讨论了仍在开发中的药物的前景。我们还推测了黑色素瘤治疗的未来,并讨论了如何使用联合和序贯治疗方法来优化未来患者的治疗。