Choi H
Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Clin Oncol (R Coll Radiol). 2017 Aug;29(8):481-488. doi: 10.1016/j.clon.2017.04.002. Epub 2017 May 12.
The first systematic response evaluation criteria were established by WHO, based on the tumor size changes shortly after the computed tomography (CT) technique became available to the daily practice. RECIST, a simplified version of WHO criteria, and its newer version, RECIST1.1 are the currently available international response evaluation criteria in solid tumors and remains based on tumor size changes. While the introduction of molecularly targeted drugs has significantly improved the survival in patient with sarcomas, the evaluation of tumor response has become more complicated. Increasing number of studies have reported the lack of shrinkage in responding tumors and raised concerns of significant underestimation of responses using RECIST. The first such observation was made on gastrointestinal stromal tumor (GIST) treated with imatinib. In GISTs responding to imatinib, the degree of contrast enhancement on CT typically decreases significantly compared with the baseline, and, regardless of whether tumors shrink, heterogeneous hyperattenuating tumors become homogeneous hypoattenuating tumors with a smaller enhancing solid component. In current oncology practice, CT is a widely accepted method of evaluating tumor response. CT images are relatively simple to acquire and can be reasonably reproduced with no significant technical obstacles. FDG-PET is highly sensitive and specific in identifying responding sarcomas. It has mostly been used as a problem solver and for those with marginally resectable GIST. More recently, the utility of whole body MRI is undergoing exploration. This article discusses the traditional size-based response evaluation criteria, and introduces new evidence based response evaluation based on changes in morphology in addition to changes in tumor size on CT images, and whole body imaging is introduced at the end.
世界卫生组织(WHO)基于计算机断层扫描(CT)技术应用于日常实践后不久肿瘤大小的变化,制定了首个系统的疗效评估标准。实体瘤疗效评价标准(RECIST)是WHO标准的简化版本,其更新版本RECIST1.1是目前可用的实体瘤国际疗效评估标准,仍基于肿瘤大小变化。虽然分子靶向药物的引入显著提高了肉瘤患者的生存率,但肿瘤疗效评估变得更加复杂。越来越多的研究报告称,有反应的肿瘤缺乏缩小,并对使用RECIST显著低估疗效表示担忧。首次此类观察是在接受伊马替尼治疗的胃肠道间质瘤(GIST)中进行的。在对伊马替尼有反应的GIST中,与基线相比,CT上的对比增强程度通常会显著降低,并且,无论肿瘤是否缩小,异质性高密度肿瘤会变成具有较小强化实性成分的均匀低密度肿瘤。在当前的肿瘤学实践中,CT是评估肿瘤疗效的广泛接受的方法。CT图像相对容易获取,并且在没有重大技术障碍的情况下可以合理再现。氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)在识别有反应的肉瘤方面具有高度敏感性和特异性。它主要用作解决问题的工具,用于那些GIST可切除性边缘的患者。最近,全身磁共振成像(MRI)的效用正在探索中。本文讨论了传统的基于大小的疗效评估标准,并介绍了基于CT图像上肿瘤大小变化以及形态学变化的新的基于证据的疗效评估,最后介绍了全身成像。