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替代值组合和指标对乳腺癌治疗中扩散加权磁共振成像预测性能和可重复性的影响:ECOG-ACRIN A6698试验结果

Impact of Alternate -Value Combinations and Metrics on the Predictive Performance and Repeatability of Diffusion-Weighted MRI in Breast Cancer Treatment: Results from the ECOG-ACRIN A6698 Trial.

作者信息

Partridge Savannah C, Steingrimsson Jon, Newitt David C, Gibbs Jessica E, Marques Helga S, Bolan Patrick J, Boss Michael A, Chenevert Thomas L, Rosen Mark A, Hylton Nola M

机构信息

Department of Radiology, University of Washington, Seattle, WA 98195, USA.

Department of Biostatistics and Center for Statistical Sciences, Brown University, Providence, RI 02912, USA.

出版信息

Tomography. 2022 Mar 4;8(2):701-717. doi: 10.3390/tomography8020058.

DOI:10.3390/tomography8020058
PMID:35314635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8938828/
Abstract

In diffusion-weighted MRI (DW-MRI), choice of b-value influences apparent diffusion coefficient (ADC) values by probing different aspects of the tissue microenvironment. As a secondary analysis of the multicenter ECOG-ACRIN A6698 trial, the purpose of this study was to investigate the impact of alternate b-value combinations on the performance and repeatability of tumor ADC as a predictive marker of breast cancer treatment response. The final analysis included 210 women who underwent standardized 4-b-value DW-MRI (b = 0/100/600/800 s/mm2) at multiple timepoints during neoadjuvant chemotherapy treatment and a subset (n = 71) who underwent test−retest scans. Centralized tumor ADC and perfusion fraction (fp) measures were performed using variable b-value combinations. Prediction of pathologic complete response (pCR) based on the mid-treatment/12-week percent change in each metric was estimated by area under the receiver operating characteristic curve (AUC). Repeatability was estimated by within-subject coefficient of variation (wCV). Results show that two-b-value ADC calculations provided non-inferior predictive value to four-b-value ADC calculations overall (AUCs = 0.60−0.61 versus AUC = 0.60) and for HR+/HER2− cancers where ADC was most predictive (AUCs = 0.75−0.78 versus AUC = 0.76), p < 0.05. Using two b-values (0/600 or 0/800 s/mm2) did not reduce ADC repeatability over the four-b-value calculation (wCVs = 4.9−5.2% versus 5.4%). The alternate metrics ADCfast (b ≤ 100 s/mm2), ADCslow (b ≥ 100 s/mm2), and fp did not improve predictive performance (AUCs = 0.54−0.60, p = 0.08−0.81), and ADCfast and fp demonstrated the lowest repeatability (wCVs = 6.71% and 12.4%, respectively). In conclusion, breast tumor ADC calculated using a simple two-b-value approach can provide comparable predictive value and repeatability to full four-b-value measurements as a marker of treatment response.

摘要

在扩散加权磁共振成像(DW-MRI)中,b值的选择通过探究组织微环境的不同方面来影响表观扩散系数(ADC)值。作为多中心ECOG-ACRIN A6698试验的二次分析,本研究的目的是调查不同b值组合对肿瘤ADC作为乳腺癌治疗反应预测标志物的性能和可重复性的影响。最终分析纳入了210名在新辅助化疗期间多个时间点接受标准化4-b值DW-MRI(b = 0/100/600/800 s/mm2)检查的女性,以及一个进行重测扫描的亚组(n = 71)。使用可变b值组合进行集中式肿瘤ADC和灌注分数(fp)测量。基于每个指标治疗中期/12周百分比变化对病理完全缓解(pCR)的预测通过受试者操作特征曲线(AUC)下的面积进行估计。可重复性通过受试者内变异系数(wCV)进行估计。结果显示,总体而言,双b值ADC计算与四b值ADC计算相比,预测价值不劣(AUC分别为0.60 - 0.61与0.60),对于ADC预测性最强的HR+/HER2-癌症也是如此(AUC分别为0.75 - 0.78与0.76),p < 0.05。使用两个b值(0/600或0/800 s/mm2)与四b值计算相比,并未降低ADC的可重复性(wCV分别为4.9 - 5.2%与5.4%)。替代指标快速ADC(b≤100 s/mm2)、慢速ADC(b≥100 s/mm2)和fp并未改善预测性能(AUC为0.54 - 0.60,p = 0.08 - 0.81),且快速ADC和fp的可重复性最低(wCV分别为6.71%和12.4%)。总之,作为治疗反应的标志物,使用简单双b值方法计算的乳腺肿瘤ADC可提供与完整四b值测量相当的预测价值和可重复性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/63b2f8e662f1/tomography-08-00058-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/3fa1cde258cc/tomography-08-00058-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/4689505307f6/tomography-08-00058-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/671675b4497e/tomography-08-00058-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/db87d7b74b9f/tomography-08-00058-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/3ffb2e6e458a/tomography-08-00058-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/32f63b5aa88f/tomography-08-00058-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/63b2f8e662f1/tomography-08-00058-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/3fa1cde258cc/tomography-08-00058-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/4689505307f6/tomography-08-00058-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/671675b4497e/tomography-08-00058-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/db87d7b74b9f/tomography-08-00058-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/3ffb2e6e458a/tomography-08-00058-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/32f63b5aa88f/tomography-08-00058-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a82/8938828/63b2f8e662f1/tomography-08-00058-g007.jpg

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