Persigehl T, Poeppel T D, Sedlaczek O
Institut für Diagnostische und Interventionelle Radiologie, Universitätsklinikum Köln, Kerpener Str. 62, 50937, Köln, Deutschland.
Klinik für Nuklearmedizin, Universitätsklinikum Essen, Hufelandstr. 55, 45122, Essen, Deutschland.
Radiologe. 2017 Oct;57(10):826-833. doi: 10.1007/s00117-017-0289-9.
CLINICAL/METHODICAL ISSUE: Modern immunotherapies in oncology show tumor response patterns differing from conventional chemotherapies including initial pseudo-progression.
Response evaluation criteria in solid tumors (RECIST 1.1) represent the currently most used response criteria for conventional chemotherapy of solid tumors. However, atypical response patterns of immunotherapies are not correctly classified using RECIST 1.1 so that the effectiveness is also incorrectly interpreted.
In order to correctly interpret these atypical response patterns, special immune-related response criteria in solid tumors (iRECIST) have been published. In contrast to RECIST 1.1 according to iRECIST an initially unconfirmed progressive disease (iUPD) requires confirmation (iCPD) in clinically stable patients by subsequent control imaging after 4-8 weeks. New lesions are separately assessed within iRECIST.
The iRECIST procedure allows a standardized objective assessment of a possible pseudo-progression which can occur in up to 10% of cases depending on the immunomodulating drug and tumor entity.
In principle, iRECIST was developed only for usage in trials testing modern immunotherapeutics.
The iRECIST procedure might also be helpful as an additional objective response criterium for clinical treatment decisions, taking the limitations into account.
临床/方法学问题:肿瘤学中的现代免疫疗法显示出与传统化疗不同的肿瘤反应模式,包括初始假性进展。
实体瘤疗效评价标准(RECIST 1.1)是目前实体瘤传统化疗最常用的疗效标准。然而,使用RECIST 1.1不能正确分类免疫疗法的非典型反应模式,因此疗效也被错误解读。
为了正确解读这些非典型反应模式,已发布了实体瘤特殊免疫相关疗效标准(iRECIST)。与RECIST 1.1不同,根据iRECIST,最初未经确认的疾病进展(iUPD)在临床稳定的患者中需要在4至8周后通过后续对照成像进行确认(iCPD)。新病灶在iRECIST中单独评估。
iRECIST程序允许对可能出现的假性进展进行标准化客观评估,根据免疫调节药物和肿瘤类型,这种情况在高达10%的病例中可能发生。
原则上,iRECIST仅为用于测试现代免疫治疗药物的试验而开发。
考虑到局限性,iRECIST程序作为临床治疗决策的额外客观疗效标准可能也有帮助。