Pembrolizumab in the treatment of metastatic non-small-cell lung cancer: patient selection and perspectives.

IF 3.3 Q1 ONCOLOGY
Lung Cancer: Targets and Therapy Pub Date : 2017-01-11 eCollection Date: 2017-01-01 DOI:10.2147/LCTT.S105678
Ashwin Somasundaram, Timothy F Burns
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引用次数: 12

Abstract

Lung cancer is the leading killer of both men and women in the US, and the 5-year survival remains poor. However, the approval of checkpoint blockade immunotherapy has shifted the treatment paradigm and provides hope for improved survival. The ability of non-small-cell lung cancer (NSCLC) to evade the host immune system can be overcome by agents such as pembrolizumab (MK-3475/lambrolizumab), which is a monoclonal antibody targeting the programmed death 1 (PD-1) receptor. In early studies, treatment with pembrolizumab led to dramatic and durable responses in select patients (PD-L1+ tumors). This remarkable efficacy lead to approval of pembrolizumab in the second-line setting as response rates were almost doubled compared to standard of care (SOC) chemotherapy. Most recently, data in the first-line setting from the KEYNOTE-024 study have redefined the SOC therapy for a selected subset of patients. In patients with ≥50% PD-L1+ tumors, pembrolizumab had a clear progression-free survival and overall survival benefit. Toxicity was mostly immune related and similar to checkpoint blockade toxicities observed in previous studies. The initial approval and subsequent studies of pembrolizumab required and utilized a companion diagnostic test, Dako's IHC 22C3, to assess PD-L1 status of patients. The evaluation and scoring system of this assay has been used by other companies as a reference to develop their own assays, which may complicate selection of patients. Finally, the impact of pembrolizumab in NSCLC is growing as evidenced by the numerous, ongoing trials open for combinations with chemotherapy, chemoradiation, other immunotherapeutics, immunomodulators, tyrosine kinase inhibitors, PI3K inhibitors, MEK inhibitors, hypomethylating agents, and histone deacetylase inhibitors. Further studies are also evaluating pembrolizumab in small-cell lung cancer and malignant pleural mesothelioma. This explosion of studies truly conveys the lack of therapeutic answers for lung cancer patients and the promise of pembrolizumab.

Abstract Image

派姆单抗治疗转移性非小细胞肺癌:患者选择和观点
肺癌是美国男性和女性的头号杀手,其5年生存率仍然很低。然而,检查点阻断免疫疗法的批准已经改变了治疗模式,并为提高生存率提供了希望。非小细胞肺癌(NSCLC)逃避宿主免疫系统的能力可以被pembrolizumab (MK-3475/lambrolizumab)等药物克服,pembrolizumab是一种靶向程序性死亡1 (PD-1)受体的单克隆抗体。在早期研究中,使用派姆单抗治疗可在特定患者(PD-L1+肿瘤)中产生显着且持久的反应。这种显著的疗效使得派姆单抗被批准用于二线治疗,因为与标准治疗(SOC)化疗相比,反应率几乎翻了一番。最近,KEYNOTE-024研究的一线数据重新定义了选定的一部分患者的SOC治疗。在PD-L1+≥50%的肿瘤患者中,派姆单抗具有明显的无进展生存期和总生存期获益。毒性主要与免疫相关,类似于先前研究中观察到的检查点阻断毒性。pembrolizumab的最初批准和后续研究需要并使用伴随诊断测试Dako的IHC 22C3来评估患者的PD-L1状态。该检测的评估和评分系统已被其他公司用作开发自己的检测方法的参考,这可能会使患者的选择复杂化。最后,pembrolizumab在NSCLC中的影响正在增长,这一点得到了大量正在进行的与化疗、放化疗、其他免疫疗法、免疫调节剂、酪氨酸激酶抑制剂、PI3K抑制剂、MEK抑制剂、低甲基化剂和组蛋白去乙酰化酶抑制剂联合使用的试验的证明。进一步的研究也在评估派姆单抗在小细胞肺癌和恶性胸膜间皮瘤中的疗效。这一爆炸性的研究真正传达了肺癌患者缺乏治疗答案和派姆单抗的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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