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免疫肿瘤治疗的第二代和第三代药物——越多越好?

Second- and third-generation drugs for immuno-oncology treatment-The more the better?

作者信息

Dempke Wolfram C M, Fenchel Klaus, Uciechowski Peter, Dale Stephen P

机构信息

Kyowa Kirin Pharmaceutical Development, Galashiels, United Kingdom; University of Munich, University Hospital of Grosshadern, Department of Haematology and Oncology, Germany.

Medical School Hamburg (MSH), Hamburg, Germany.

出版信息

Eur J Cancer. 2017 Mar;74:55-72. doi: 10.1016/j.ejca.2017.01.001. Epub 2017 Feb 10.

Abstract

Recent success in cancer immunotherapy (anti-CTLA-4, anti-PD1/PD-L1) has confirmed the hypothesis that the immune system can control many cancers across various histologies, in some cases producing durable responses in a way not seen with many small-molecule drugs. However, only less than 25% of all patients do respond to immuno-oncology drugs and several resistance mechanisms have been identified (e.g. T-cell exhaustion, overexpression of caspase-8 and β-catenin, PD-1/PD-L1 gene amplification, MHC-I/II mutations). To improve response rates and to overcome resistance, novel second- and third-generation immuno-oncology drugs are currently evaluated in ongoing phase I/II trials (either alone or in combination) including novel inhibitory compounds (e.g. TIM-3, VISTA, LAG-3, IDO, KIR) and newly developed co-stimulatory antibodies (e.g. CD40, GITR, OX40, CD137, ICOS). It is important to note that co-stimulatory agents strikingly differ in their proposed mechanism of action compared with monoclonal antibodies that accomplish immune activation by blocking negative checkpoint molecules such as CTLA-4 or PD-1/PD-1 or others. Indeed, the prospect of combining agonistic with antagonistic agents is enticing and represents a real immunologic opportunity to 'step on the gas' while 'cutting the brakes', although this strategy as a novel cancer therapy has not been universally endorsed so far. Concerns include the prospect of triggering cytokine-release syndromes, autoimmune reactions and hyper immune stimulation leading to activation-induced cell death or tolerance, however, toxicity has not been a major issue in the clinical trials reported so far. Although initial phase I/II clinical trials of agonistic and novel antagonistic drugs have shown highly promising results in the absence of disabling toxicity, both in single-agent studies and in combination with chemotherapy or other immune system targeting drugs; however, numerous questions remain about dose, schedule, route of administration and formulation as well as identifying the appropriate patient populations. In our view, with such a wealth of potential mechanisms of action and with the ability to fine-tune monoclonal antibody structure and function to suit particular requirements, the second and third wave of immuno-oncology drugs are likely to provide rapid advances with new combinations of novel immunotherapy (especially co-stimulatory antibodies). Here, we will review the mechanisms of action and the clinical data of these new antibodies and discuss the major issues facing this rapidly evolving field.

摘要

癌症免疫疗法(抗CTLA-4、抗PD1/PD-L1)最近取得的成功证实了这样一个假设,即免疫系统可以控制多种组织学类型的许多癌症,在某些情况下会产生持久反应,这是许多小分子药物所未见的。然而,所有患者中只有不到25%对免疫肿瘤药物有反应,并且已经确定了几种耐药机制(例如T细胞耗竭、caspase-8和β-连环蛋白的过表达、PD-1/PD-L1基因扩增、MHC-I/II突变)。为了提高反应率并克服耐药性,目前正在进行的I/II期试验(单独或联合使用)中评估新型第二代和第三代免疫肿瘤药物,包括新型抑制性化合物(例如TIM-3、VISTA、LAG-3、IDO、KIR)和新开发的共刺激抗体(例如CD40、GITR、OX40、CD137、ICOS)。需要注意的是,与通过阻断负性检查点分子(如CTLA-4或PD-1/PD-L1等)来实现免疫激活的单克隆抗体相比,共刺激剂的作用机制明显不同。确实,将激动剂与拮抗剂联合使用的前景很诱人,代表了一种真正的免疫学机会,即“踩油门”的同时“踩刹车”,尽管作为一种新型癌症疗法,这一策略目前尚未得到普遍认可。人们担心会引发细胞因子释放综合征、自身免疫反应以及过度免疫刺激导致激活诱导的细胞死亡或耐受,然而,毒性在目前报道的临床试验中尚未成为一个主要问题。尽管激动剂和新型拮抗剂药物的初始I/II期临床试验在没有严重毒性的情况下显示出非常有前景的结果,无论是在单药研究中还是与化疗或其他靶向免疫系统的药物联合使用时;然而,关于剂量、给药方案、给药途径和制剂以及确定合适的患者群体仍有许多问题。我们认为,有如此丰富的潜在作用机制,并且有能力微调单克隆抗体的结构和功能以满足特定要求,第二代和第三代免疫肿瘤药物可能会通过新型免疫疗法(尤其是共刺激抗体)的新组合迅速取得进展。在此,我们将综述这些新抗体的作用机制和临床数据,并讨论这个快速发展领域面临的主要问题。

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