Steininger Julian, Gellrich Frank Friedrich, Schulz Alexander, Westphal Dana, Beissert Stefan, Meier Friedegund
Skin Cancer Center at the University Cancer Center and National Center for Tumor Diseases, Department of Dermatology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Cancers (Basel). 2021 Mar 20;13(6):1430. doi: 10.3390/cancers13061430.
This decade has brought significant survival improvement in patients with metastatic melanoma with targeted therapies and immunotherapies. As our understanding of the mechanisms of action of these therapeutics evolves, even more impressive therapeutic success is being achieved through various combination strategies, including combinations of different immunotherapies as well as with other modalities. This review summarizes prospectively and retrospectively generated clinical evidence on modern melanoma therapy, focusing on immunotherapy and targeted therapy with BRAF kinase inhibitors and MEK kinase inhibitors (BRAF/MEK inhibitors), including recent data presented at major conference meetings. The combination of the anti-PD-1 directed monoclonal antibody nivolumab and of the CTLA-4 antagonist ipilimumab achieves unprecedented 5-year overall survival (OS) rates above 50%; however, toxicity is high. For PD-1 monotherapy (nivolumab or pembrolizumab), toxicities are in general well manageable. Today, novel combinations of such immune checkpoint inhibitors (ICIs) are under investigation, for example with cytokines and oncolytic viruses (i.e., pegylated interleukin-2, talimogene laherparepvec). Furthermore, current studies investigate the combined or sequential use of ICIs plus BRAF/MEK inhibitors. Several studies focus particularly on poor prognosis patients, as e.g., on anti-PD-1 refractory melanoma, patients with brain metastases, or uveal melanoma. It is hoped, on the road to cure, that these new approaches further improve long term survival in patients with advanced or metastatic melanoma.
在这十年间,靶向治疗和免疫治疗显著提高了转移性黑色素瘤患者的生存率。随着我们对这些治疗方法作用机制的理解不断深入,通过各种联合策略,包括不同免疫疗法之间以及与其他治疗方式的联合,取得了更加令人瞩目的治疗成果。本综述总结了前瞻性和回顾性产生的关于现代黑色素瘤治疗的临床证据,重点关注免疫治疗以及BRAF激酶抑制剂和MEK激酶抑制剂(BRAF/MEK抑制剂)的靶向治疗,包括在主要会议上展示的最新数据。抗PD-1单克隆抗体纳武利尤单抗与CTLA-4拮抗剂伊匹木单抗联合使用,实现了前所未有的5年总生存率(OS)超过50%;然而,毒性较高。对于PD-1单药治疗(纳武利尤单抗或帕博利珠单抗),毒性总体上易于控制。如今,此类免疫检查点抑制剂(ICI)的新型联合疗法正在研究中,例如与细胞因子和溶瘤病毒联合(即聚乙二醇化白细胞介素-2、talimogene laherparepvec)。此外,目前的研究正在探究ICI与BRAF/MEK抑制剂联合或序贯使用的情况。多项研究特别关注预后较差的患者,例如抗PD-1难治性黑色素瘤患者、脑转移患者或葡萄膜黑色素瘤患者。在攻克黑色素瘤的道路上,希望这些新方法能进一步提高晚期或转移性黑色素瘤患者的长期生存率。