Digklia Antonia, Michielin Olivier
Department of Oncology, Centre Hospitalier Universitaire Vaudois, Bugnon 46, 1011 Lausanne, Switzerland.
Melanoma Manag. 2016 Sep;3(3):217-229. doi: 10.2217/mmt-2016-0026. Epub 2016 Aug 22.
The past decade has witnessed impressive new developments for the treatment of melanoma. The discovery of key oncogenic driver mutations, upon which tumor establishment and progression are dependent, changed the prognosis of patients with stage IV disease. Extensive preclinical and clinical studies have shown high response rates and survival benefits over conventional chemotherapies provided by target-specific inhibitors of BRAF- or NRAS-activating mutations. Recent genomic analyses of melanoma have also given new potentially targetable driver mutations. In addition, the quickened pace of development of immune checkpoint inhibitors for the treatment of melanoma offers the unique opportunity to provide a long-term clinical benefit. In this emerging era, predictive biomarkers for the selection of patients are required to help us develop an optimal therapeutic strategy.
过去十年见证了黑色素瘤治疗方面令人瞩目的新进展。关键致癌驱动基因突变的发现改变了IV期疾病患者的预后,肿瘤的发生和进展依赖于这些突变。广泛的临床前和临床研究表明,针对BRAF或NRAS激活突变的特异性靶向抑制剂相比于传统化疗,具有更高的缓解率和生存获益。黑色素瘤的最新基因组分析也发现了新的潜在可靶向驱动基因突变。此外,用于治疗黑色素瘤的免疫检查点抑制剂研发步伐加快,提供了带来长期临床获益的独特机会。在这个新兴时代,需要有预测性生物标志物来挑选患者,以帮助我们制定最佳治疗策略。