Department of Research, Molecular Immunology Unit Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Department of Medical Oncology, Thoracic Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Future Oncol. 2020 Aug;16(23):1707-1713. doi: 10.2217/fon-2020-0186. Epub 2020 Jul 20.
In the immunoncology era, an acceleration of tumor growth upon immune checkpoint inhibitors (ICI), defined as hyperprogressive disease (HPD) has been observed across different cancers. Although in non-small-cell lung cancer, most of the available evidence regarding HPD has been reported for patients treated with single agent PD-1 and PD-L1 inhibitors, in retrospective series a variable proportion of patients receiving ICI combinations also experienced HPD. Similarly, the shape of survival curves and the progression rates in clinical trials testing combinations of PD-1/PD-L1 inhibitors and anti-CTLA-4 agents suggest the occurrence of HPD. Few data are available regarding pseudoprogression upon ICI combinations. However, considering that pseudoprogression has been reported for anti-PD-1/PD-L1 agents and for CTLA-4 inhibitors separately, it is likely that it may occur also upon combinations of these two classes of drugs.
在免疫肿瘤学时代,在不同的癌症中观察到免疫检查点抑制剂(ICI)加速肿瘤生长,定义为超进展性疾病(HPD)。尽管在非小细胞肺癌中,大多数关于 HPD 的可用证据都是针对接受单一 PD-1 和 PD-L1 抑制剂治疗的患者报告的,但在回顾性系列研究中,接受 ICI 联合治疗的患者中也有不同比例的患者出现 HPD。同样,临床试验中测试 PD-1/PD-L1 抑制剂和抗 CTLA-4 药物组合的生存曲线形状和进展率表明 HPD 的发生。关于 ICI 联合治疗后的假性进展的数据很少。然而,考虑到抗 PD-1/PD-L1 药物和 CTLA-4 抑制剂分别报告了假性进展,因此这两种药物联合治疗后也可能发生假性进展。