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帕博利珠单抗治疗转移性非小细胞肺癌:患者选择与展望

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

作者信息

Somasundaram Ashwin, Burns Timothy F

机构信息

Division of Hematology/Oncology, Department of Medicine, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.

出版信息

Lung Cancer (Auckl). 2017 Jan 11;8:1-11. doi: 10.2147/LCTT.S105678. eCollection 2017.

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.

摘要

肺癌是美国男性和女性的主要杀手,5年生存率仍然很低。然而,检查点阻断免疫疗法的获批改变了治疗模式,并为提高生存率带来了希望。非小细胞肺癌(NSCLC)逃避宿主免疫系统的能力可以通过派姆单抗(MK-3475/兰布单抗)等药物来克服,派姆单抗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,派姆单抗治疗在部分患者(PD-L1阳性肿瘤)中导致了显著且持久的反应。这种显著的疗效使得派姆单抗在二线治疗中获批,因为与标准治疗(SOC)化疗相比,缓解率几乎提高了一倍。最近,KEYNOTE-024研究一线治疗的数据重新定义了特定亚组患者的SOC疗法。在PD-L1阳性肿瘤≥50%的患者中,派姆单抗具有明显的无进展生存期和总生存期获益。毒性大多与免疫相关,与先前研究中观察到的检查点阻断毒性相似。派姆单抗的初始获批及后续研究需要并使用了伴随诊断检测——达科公司的免疫组化22C3检测,以评估患者的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身检测方法的参考,这可能会使患者选择变得复杂。最后,派姆单抗在NSCLC中的影响不断扩大,这从众多正在进行的与化疗、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脱乙酰酶抑制剂联合使用的试验中可见一斑。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作用。这些大量的研究真正表明了肺癌患者缺乏有效的治疗方法以及派姆单抗带来的希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/5342609/2562ee8e4b09/lctt-8-001Fig1.jpg

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