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临床试验中常规临床解读与正式 RECIST 1.1 解读评估进展性疾病的差异。

Discrepant Assessments of Progressive Disease in Clinical Trials between Routine Clinical Reads and Formal RECIST 1.1 Interpretations.

机构信息

From the Edward Mallinckrodt Institute of Radiology and Alvin J. Siteman Cancer Center, Washington University School of Medicine, 510 S Kingshighway Blvd, St Louis, MO 63110.

出版信息

Radiol Imaging Cancer. 2023 Sep;5(5):e230001. doi: 10.1148/rycan.230001.

Abstract

Purpose To analyze the frequency of discrepant interpretations of progressive disease (PD) between routine clinical and formal Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 interpretations in patients enrolled in solid tumor clinical trials and investigate the causes of discordance. Materials and Methods This retrospective study included patients in solid tumor clinical trials undergoing imaging response assessments based on RECIST 1.1 from January to July 2021. Routine clinical interpretations (RCIs) performed as part of standard workflow and not requiring formal use of any established response criteria were compared with separate local core laboratory interpretations (CLIs) by specially trained radiologists who used software that tracks target lesion measurements, changes in nontarget lesions, and appearance of new lesions longitudinally. The comparison focused on discordant interpretations of PD. Results Among 1053 patients who had both RCIs and CLIs performed, PD was diagnosed on one or both reads in 327 patients (median age, 63.6 [range, 22.4-83.2] years; 57.8% female patients). The RCIs and CLIs agreed with PD status in 65% (213 of 327) of assessments. In 32% (105 of 327) of assessments, RCIs overdiagnosed PD when CLIs diagnosed stable disease, and in 3% (nine of 327), CLIs diagnosed PD when RCIs diagnosed stable disease. Reasons for discrepant RCIs of PD included erroneous target lesion measurements (58%, 61 of 105), erroneous diagnosis of nontarget progression (30%, 32 of 105), and misclassification of new lesions as cancer (11%, 12 of 105). Most patients (93%, 98 of 105) with RCI overdiagnosis of PD remained in the clinical trial for one or more treatment cycles. Conclusion PD was frequently overdiagnosed on RCIs versus formal RECIST 1.1 CLIs which could result in patients removed from the clinical trial inappropriately. Oncology, Cancer, Tumor Response, MR Imaging, CT © RSNA, 2023 See also commentary by Margolis and Ruchalski in this issue.

摘要

目的

分析实体瘤临床试验中常规临床与正式实体瘤反应评估标准 1.1(RECIST 1.1)对进展性疾病(PD)的解读存在差异的频率,并探讨差异产生的原因。

材料与方法

本回顾性研究纳入了 2021 年 1 月至 7 月期间接受基于 RECIST 1.1 的影像学反应评估的实体瘤临床试验患者。将作为标准工作流程一部分进行的常规临床解读(RCIs)与专门接受培训的放射科医生使用软件进行的单独的局部核心实验室解读(CLIs)进行比较,该软件可追踪目标病变测量值、非目标病变变化和新病变的出现情况。比较重点为 PD 的不一致解读。

结果

在 1053 例同时进行了 RCIs 和 CLIs 的患者中,327 例(中位年龄,63.6 [范围,22.4-83.2] 岁;57.8%为女性)在一次或两次检查中诊断为 PD。RCIs 与 65%(327 例中的 213 例)评估的 PD 状态一致。在 32%(327 例中的 105 例)评估中,RCIs 过度诊断 PD 而 CLIs 诊断为稳定疾病,在 3%(327 例中的 9 例)评估中,CLIs 诊断为 PD 而 RCIs 诊断为稳定疾病。RCIs 对 PD 不一致的原因包括目标病变测量错误(58%,61/105)、非目标进展错误诊断(30%,32/105)和新病变错误分类为癌症(11%,12/105)。大多数(93%,98/105)RCIs 过度诊断 PD 的患者在临床试验中接受了一个或多个治疗周期的治疗。

结论

RCIs 对 PD 的诊断比正式 RECIST 1.1 CLIs 更频繁,这可能导致患者不恰当地从临床试验中被剔除。

肿瘤学、癌症、肿瘤反应、磁共振成像、计算机断层扫描

©RSNA,2023

也可参见本期 Margolis 和 Ruchalski 的评论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/876c/10546354/4c86b8a9e266/rycan.230001.VA.jpg

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