Pembrolizumab for the treatment of advanced melanoma

被引:12
作者
Burns, Michael C. [1 ]
O'donnell, Aidan [1 ]
Puzanov, Igor [2 ]
机构
[1] Vanderbilt Univ, Dept Med, Sch Med, Nashville, TN USA
[2] Vanderbilt Univ, Med Ctr, Div Hematol Oncol, Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
来源
EXPERT OPINION ON ORPHAN DRUGS | 2016年 / 4卷 / 08期
关键词
Immunotherapy; pembrolizumab; programmed death-1; programmed death-ligand 1; ANTI-PD-1; MONOCLONAL-ANTIBODY; METASTATIC MELANOMA; OPEN-LABEL; PHASE-II; IPILIMUMAB; DABRAFENIB; SURVIVAL; VEMURAFENIB; NIVOLUMAB; CHEMOTHERAPY;
D O I
10.1080/21678707.2016.1191348
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Since 2010 multiple targeted therapies and immunotherapies have been approved for the treatment of advanced melanoma. Pembrolizumab, a humanized monoclonal antibody directed against programed death receptor 1 has shown significant activity in advanced melanoma resulting in its approval first as post-ipilimumab and subsequently as frontline treatment.Areas covered: This article reviews the approved agents for the treatment of advanced melanoma with a focus on the preclinical and clinical evidence for the use of pembrolizumab in this setting. Primary emphasis is given to the clinical development of pembrolizumab, including phase I-III trials. Finally, we explore the role of pembrolizumab in combination with other therapies and ongoing investigations into its effectiveness in expanded patient populations.Expert opinion: Pembrolizumab provides durable responses and represents a major advancement in the treatment options for patients with advanced melanoma. Early studies of pembrolizumab in combination with other therapeutic agents have generated significant interest and further investigations including advanced clinical trials are warranted to evaluate safety and potential improved outcomes. Pembrolizumab and other immune checkpoint inhibitors are likely to play an expanded role in the treatment of advanced melanoma and other solid tumors over the next decade.
引用
收藏
页码:867 / 873
页数:7
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