Dual-energy CT iodine concentration as a biomarker for immunotherapy treatment response in metastatic melanoma and renal cell carcinoma patients.

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Radiology Pub Date : 2025-08-01 Epub Date: 2025-01-28 DOI:10.1007/s00330-025-11351-4
Natalie Wiley, Mladen Zecevic, Vivian Ho, Matthew J Stolzberg, Danielle Cox, Erik V Soloff, Evan Hall, Carolyn L Wang
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Abstract

Objective: To investigate the predictive value of tumor iodine concentration obtained with dual-energy CT (DECT) for treatment response in patients treated with immune checkpoint inhibitors (ICI).

Materials and methods: Retrospective single-center study of consecutive metastatic melanoma and renal cell carcinoma (RCC) patients undergoing first-line ICI treatment. The iodine concentration measurement time points include prior to initiation of therapy (baseline [BL]), after initiation (follow-up [FU1]), and either time point nearest to 12 months or at time of progression (final follow-up [FFU]). Target lesion DECT-based whole-volume tumor normalized iodine concentration average (NICave) and size measurements were obtained. Reference standard was individual lesion FFU status categorized as responders or nonresponders per RECIST 1.1. Logistic regression model assessed NICave change and FU1 lesion response as predictors of FFU lesion outcome. Model's performance was summarized with AUC. Intraclass correlation coefficient (ICC) summarized inter-rater agreement of NICave.

Results: Forty-six patients were included (mean age 61 ± 11 years, 12 women; 16 melanoma). Sixty-four of 175 target lesions were confirmed nonresponders at FFU. In a multivariable model, lesion status at FU1 (odds ratio [OR]: 27.4, p < 0.001) and changes in NICave from BL to FU1 (OR: 2.42 per 1-SD increase, p = 0.019) were significant predictors of lesion status at FFU. The model's AUC was 0.86 (95% CI: 0.76-0.93). Inter-rater reliability of NICave was 0.98 (95% CI: 0.97-0.99).

Conclusions: Changes in iodine concentration from baseline to first follow-up improve identification of delayed responding metastatic melanoma and RCC lesions treated with immune checkpoint inhibitor, initially classified as nonresponders by size change.

Key points: Question How can pseudoprogression/delayed treatment response in metastatic renal cell carcinoma (RCC) and melanoma patients on first-line immune checkpoint inhibitors be accurately identified? Findings Combining iodine concentration change from Dual-energy CT (baseline to first follow-up) with RECIST-based lesion size change improved prediction of final lesion outcome. Clinical relevance DECT-based whole-volume tumor iodine concentration for target lesions is useful as a predictive imaging biomarker for distinguishing delayed response from true progression in patients with metastatic RCC and melanoma treated with first-line immune checkpoint inhibitors.

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双能CT碘浓度作为转移性黑色素瘤和肾细胞癌患者免疫治疗反应的生物标志物
目的:探讨双能CT (DECT)检测肿瘤碘浓度对免疫检查点抑制剂(ICI)患者治疗反应的预测价值。材料和方法:对连续转移性黑色素瘤和肾细胞癌(RCC)患者进行一线ICI治疗的回顾性单中心研究。碘浓度测量时间点包括开始治疗前(基线[BL]),开始治疗后(随访[FU1]),以及最接近12个月或进展时的时间点(最终随访[FFU])。靶病变基于ct的全体积肿瘤归一化碘浓度平均值(NICave)和尺寸测量。参考标准是根据RECIST 1.1将单个病变FFU状态分类为应答或无应答。Logistic回归模型评估NICave变化和FU1病变反应作为FFU病变结局的预测因子。用AUC来总结模型的性能。类内相关系数(Intraclass correlation coefficient, ICC)总结了NICave的类间一致性。结果:纳入46例患者(平均年龄61±11岁,女性12例;16黑素瘤)。175个靶病变中有64个经FFU治疗无反应。结论:从基线到第一次随访碘浓度的变化改善了免疫检查点抑制剂治疗延迟反应的转移性黑色素瘤和RCC病变的识别,最初根据大小变化将其归类为无反应。如何准确识别使用一线免疫检查点抑制剂的转移性肾细胞癌(RCC)和黑色素瘤患者的假进展/延迟治疗反应?结果:双能CT(基线至首次随访)碘浓度变化与基于recist的病变大小变化相结合可改善对最终病变结局的预测。在接受一线免疫检查点抑制剂治疗的转移性RCC和黑色素瘤患者中,基于ct的靶病变全体积肿瘤碘浓度可作为一种预测性成像生物标志物,用于区分延迟反应和真正进展。
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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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