Oncology 2, Istituto Oncologico Veneto IRCCS, Padova, Italy.
Oncology 2, Istituto Oncologico Veneto IRCCS, Padova, Italy.
Cancer Treat Rev. 2020 Jul;87:102031. doi: 10.1016/j.ctrv.2020.102031. Epub 2020 May 16.
Immune checkpoint inhibitors (ICIs) targeting programmed death 1 (PD-1) and PD-ligand 1 (PD-L1) quickly subverted the standard of treatment in Non-Small Cell Lung Cancer (NSCLC), where they were first introduced in all comers previously treated advanced/metastatic NSCLC patients and subsequently in the first line of PD-L1 selected cases of metastatic and locally advanced disease. Treatment algorithm is an evolving landscape, where the introduction of front-line ICIs, with or without chemotherapy, unavoidably influences the following treatment lines. In this context, medical oncologists are currently facing many unclear issues, which have been not clarified so far by available data. Effectiveness and safety in special populations underrepresented in clinical trials - such as elderly, poor PS, hepatitis or human immunodeficiency virus-affected patients - are only a part of the unexplored side of ICIs in the real world. Indeed, pivotal randomized clinical trials (RCTs) often lack of external validity because eligibility criteria exclude some patient subgroups commonly treated in real-world clinical practice. Similarly, cost-effectiveness and sustainability of these innovative agents are important issues to be considered in the real-world. Though affected by several limitations, real-world evidence (RWE) studies allow to collect data regarding overall treated patients in clinical practice according to local authority regulations, overcoming the intrinsic limits of RCTs. The present review focuses on RWE about ICIs in lung cancer treatment, with particular reference to special patient populations, and discusses potential application of real-world data in a potential innovative drug development model.
免疫检查点抑制剂 (ICIs) 靶向程序性死亡 1 (PD-1) 和 PD-配体 1 (PD-L1),迅速颠覆了非小细胞肺癌 (NSCLC) 的治疗标准,最初在所有接受过治疗的晚期/转移性 NSCLC 患者中使用,随后在 PD-L1 选择的转移性和局部晚期疾病患者中使用。治疗方案是一个不断发展的领域,一线 ICIs 的引入(无论是否联合化疗)不可避免地影响了后续的治疗线。在这种情况下,肿瘤内科医生目前面临着许多尚未被现有数据澄清的不明问题。临床试验中代表性不足的特殊人群(如老年、较差的 PS、肝炎或艾滋病毒感染患者)的有效性和安全性只是 ICI 在真实世界中尚未探索的部分。事实上,关键性随机临床试验 (RCT) 通常缺乏外部有效性,因为入选标准排除了一些在真实世界临床实践中经常治疗的患者亚组。同样,这些创新药物的成本效益和可持续性也是在真实世界中需要考虑的重要问题。尽管受到多种限制,真实世界证据 (RWE) 研究允许根据当地当局的规定收集关于临床实践中总体治疗患者的数据,从而克服 RCTs 的内在局限性。本综述重点介绍了关于肺癌治疗中 ICI 的 RWE,特别是特殊患者群体,并讨论了真实世界数据在潜在创新药物开发模型中的潜在应用。