Presented by John A. Thompson, MD, Division of Medical Oncology, University of Washington School of Medicine/Seattle Cancer Care Alliance, Seattle, Washington.
J Natl Compr Canc Netw. 2016 May;14(5 Suppl):638-40. doi: 10.6004/jnccn.2016.0180.
Over the past 5 years, a host of new agents have radically changed the therapeutic landscape in advanced melanoma; gone are the days when the only active agents were interferon and dacarbazine. Nearly 25 years ago, few patients with stage IV melanoma reached 2-year survival; today, these survival curves have risen substantially. At the NCCN 21st Annual Conference, John A. Thompson, MD, discussed updates with longer duration of patient follow-up for immune checkpoint therapies. He also reviewed some of the newer approvals in advanced melanoma, including the combination of ipilimumab and nivolumab, high-dose ipilimumab, the oncolytic virus therapy talimogene laherparepvec, and the molecularly targeted combination of the BRAF and MEK inhibitors vemurafenib and cobimetinib.
在过去的 5 年中,许多新型药物彻底改变了晚期黑色素瘤的治疗格局;曾经只有干扰素和达卡巴嗪是有效的药物。大约 25 年前,很少有 IV 期黑色素瘤患者能存活 2 年;而如今,这些生存曲线已显著提高。在 NCCN 第 21 届年会上,John A. Thompson, MD 讨论了免疫检查点治疗具有更长随访时间的更新信息。他还回顾了晚期黑色素瘤的一些新批准药物,包括 ipilimumab 和 nivolumab 的联合用药、高剂量 ipilimumab、溶瘤病毒疗法 talimogene laherparepvec,以及 BRAF 和 MEK 抑制剂 vemurafenib 和 cobimetinib 的分子靶向联合用药。