Schneider Hannah, Illert Anne-Lena, Bamberg Fabian, Eisenblätter Michel
Klinik für Diagnostische und Interventionelle Radiologie, Universitätsklinikum Freiburg, Hugstetter Str. 55, 79106, Freiburg, Deutschland.
Klinik für Innere Medizin I - Onkologie, Universitätsklinikum Freiburg, Freiburg, Deutschland.
Radiologe. 2020 Aug;60(8):711-720. doi: 10.1007/s00117-020-00726-x.
Cancer immunotherapies play an increasing role in the treatment of advanced cancer. In a subset of patients, atypical response patterns and unconventional adverse events make diagnostic evaluation challenging for radiologists.
In this article, we provide a review of the possibilities and limitations of imaging methods in monitoring immunotherapies, discuss the phenomena of pseudoprogression and hyperprogression, and introduce iRECIST as an evaluation standard for clinical studies with immunotherapies. In addition, we describe the most notable adverse events and their imaging features.
This article is based on reviews and studies published since 2009. We used PubMed for the literature search and included the following search terms: "immunotherapy", "checkpoint inhibitor", "pseudoprogression", "iRECIST" and "immune related adverse events".
With an incidence of up to 10%, pseudoprogression is a rare phenomenon. Currently, differentiation between pseudoprogression and true progressive disease is only possible by follow-up examinations. iRECIST, published in 2017, introduced immune unconfirmed progressive disease (iUPD) and immune confirmed progressive disease (iCPD) as new categories of therapeutic response. There is still no consensus on the time interval between examinations. Crucial adverse events include hypophysitis and pneumonitis, whereby the latter may present as different patterns of interstitial pneumonia making it difficult to differentiate between drug toxicity, infection, and tumor progression.
癌症免疫疗法在晚期癌症治疗中发挥着越来越重要的作用。在一部分患者中,非典型反应模式和非常规不良事件给放射科医生的诊断评估带来了挑战。
在本文中,我们综述了成像方法在监测免疫疗法中的可能性和局限性,讨论了假性进展和超进展现象,并介绍了iRECIST作为免疫疗法临床研究的评估标准。此外,我们描述了最显著的不良事件及其成像特征。
本文基于2009年以来发表的综述和研究。我们使用PubMed进行文献检索,检索词包括:“免疫疗法”、“检查点抑制剂”、“假性进展”、“iRECIST”和“免疫相关不良事件”。
假性进展发生率高达10%,是一种罕见现象。目前,仅通过随访检查才能区分假性进展和真正的疾病进展。2017年发布的iRECIST引入了免疫未确认进展性疾病(iUPD)和免疫确认进展性疾病(iCPD)作为治疗反应的新类别。检查之间的时间间隔仍未达成共识。关键不良事件包括垂体炎和肺炎,其中后者可能表现为不同类型的间质性肺炎,难以区分药物毒性、感染和肿瘤进展。