Houdek Š, Büchler T, Kindlová E
Klin Onkol. 2017 Winter;30(Supplementum3):32-39. doi: 10.14735/amko20173S32.
Immunotherapy is a relatively new and developing modality in oncological treatment, which may significantly improve treatment results for some patients with malignant tumors. With the increasing number of clinical trials, the demand for a suitable tool to assess and compare treatment responses is growing. Currently, the most common response assessment system for solid tumors is RECIST (response Evaluation Criteria in Solid Tumors) version 1.1. However, in immuno-oncology, a small percentage of patients manifest a new response pattern termed pseudoprogression, in which, after the initial increase in tumor burden or after the discovery of new lesions, a response or at least a prolonged stabilization of the disease can occur. This patient group would be included in the progression category when using RECIST 1.1 and effective treatment would be discontinued. Therefore, iRECIST criteria were established to capture the phenomenon of pseudoprogression, the need for PD confirmation (according to RECIST 1.1) was introduced, and changes were made in the evaluation of new lesions.
The present work introduces criteria for the evaluation of oncological responses in solid tumors using RECIST version 1.1 and iRECIST immunotherapy variant (including a brief overview of previous immune criteria). These criteria are compared in an immuno-oncological context and their potential pitfalls are discussed.
iRECIST criteria were established by expert consensus; however, sufficient data for final validation has not yet been collected. As a result, RECIST 1.1 should be the primary assessment system in immuno-oncology. The use of iRECIST should be reserved for research purposes (testing and validation). Distinguishing pseudoprogression from true PD in patients treated with immunotherapy remains a major challenge in oncological imaging.Key words: RECIST - response criteria - immunotherapy - measurement - tumor burden The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.Submitted: 24. 9. 2017Accepted: 3. 10. 2017.
免疫疗法是肿瘤治疗中一种相对较新且不断发展的治疗方式,它可能显著改善一些恶性肿瘤患者的治疗效果。随着临床试验数量的增加,对评估和比较治疗反应的合适工具的需求也在增长。目前,实体瘤最常用的反应评估系统是实体瘤疗效评价标准(RECIST)1.1版。然而,在免疫肿瘤学中,一小部分患者表现出一种新的反应模式,称为假性进展,即在肿瘤负荷最初增加或发现新病灶后,可能会出现反应或至少疾病长期稳定。使用RECIST 1.1时,这部分患者会被归类为进展类别,有效的治疗将被中断。因此,建立了iRECIST标准以捕捉假性进展现象,引入了根据RECIST 1.1进行疾病进展(PD)确认的必要性,并对新病灶的评估进行了更改。
本研究介绍了使用RECIST 1.1版和iRECIST免疫疗法变体评估实体瘤肿瘤反应的标准(包括对先前免疫标准的简要概述)。在免疫肿瘤学背景下对这些标准进行了比较,并讨论了它们潜在的缺陷。
iRECIST标准是通过专家共识建立的;然而,尚未收集到足够的最终验证数据。因此,RECIST 1.1应作为免疫肿瘤学中的主要评估系统。iRECIST的使用应仅限于研究目的(测试和验证)。在接受免疫治疗的患者中区分假性进展和真正的疾病进展仍然是肿瘤影像学中的一项重大挑战。关键词:RECIST - 反应标准 - 免疫疗法 - 测量 - 肿瘤负荷 作者声明他们在研究中使用的药物、产品或服务方面没有潜在的利益冲突。编辑委员会声明该手稿符合ICMJE对生物医学论文的建议。提交日期:2017年9月24日 接受日期:2017年10月3日