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本文引用的文献

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Predictive Risk Factors for Early Recurrence of Stage pIIIA-N2 Non-Small Cell Lung Cancer.pIIIA-N2期非小细胞肺癌早期复发的预测危险因素
Cancer Manag Res. 2021 Nov 18;13:8651-8661. doi: 10.2147/CMAR.S337830. eCollection 2021.
2
Radiomics in lung cancer for oncologists.肿瘤学家视角下的肺癌影像组学
J Clin Transl Res. 2020 Sep 2;6(4):127-134. eCollection 2020 Oct 29.
3
[Formula: see text]: deep learning-based radiomics for the time-to-event outcome prediction in lung cancer.[公式:见正文]:基于深度学习的肺癌生存时间预测放射组学。
Sci Rep. 2020 Jul 23;10(1):12366. doi: 10.1038/s41598-020-69106-8.
4
Application and limitation of radiomics approach to prognostic prediction for lung stereotactic body radiotherapy using breath-hold CT images with random survival forest: A multi-institutional study.基于屏气CT图像并采用随机生存森林的放射组学方法在肺立体定向体部放疗预后预测中的应用及局限性:一项多机构研究
Med Phys. 2020 Sep;47(9):4634-4643. doi: 10.1002/mp.14380. Epub 2020 Aug 2.
5
Preoperative CT-based Deep Learning Model for Predicting Disease-Free Survival in Patients with Lung Adenocarcinomas.基于术前 CT 的深度学习模型预测肺腺癌患者无病生存。
Radiology. 2020 Jul;296(1):216-224. doi: 10.1148/radiol.2020192764. Epub 2020 May 12.
6
Deep segmentation networks predict survival of non-small cell lung cancer.深度分割网络预测非小细胞肺癌的生存率。
Sci Rep. 2019 Nov 21;9(1):17286. doi: 10.1038/s41598-019-53461-2.
7
Bone Marrow and Tumor Radiomics at F-FDG PET/CT: Impact on Outcome Prediction in Non-Small Cell Lung Cancer.骨髓和肿瘤 CT 体层摄影术 F-FDG 摄取的放射组学:对非小细胞肺癌预后预测的影响。
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8
CT Radiomics Signature of Tumor and Peritumoral Lung Parenchyma to Predict Nonsmall Cell Lung Cancer Postsurgical Recurrence Risk.CT 影像组学肿瘤及瘤周肺实质特征预测非小细胞肺癌术后复发风险
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9
[18F] FDG Positron Emission Tomography (PET) Tumor and Penumbra Imaging Features Predict Recurrence in Non-Small Cell Lung Cancer.[18F]氟代脱氧葡萄糖正电子发射断层扫描(PET)的肿瘤及半暗带成像特征可预测非小细胞肺癌的复发情况。
Tomography. 2019 Mar;5(1):145-153. doi: 10.18383/j.tom.2018.00026.
10
Radiomics: the facts and the challenges of image analysis.放射组学:图像分析的现状与挑战
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使用多模态放射组学和随机生存森林预测肺癌患者的复发风险。

Predicting recurrence risks in lung cancer patients using multimodal radiomics and random survival forests.

作者信息

Christie Jaryd R, Daher Omar, Abdelrazek Mohamed, Romine Perrin E, Malthaner Richard A, Qiabi Mehdi, Nayak Rahul, Napel Sandy, Nair Viswam S, Mattonen Sarah A

机构信息

Western University, Department of Medical Biophysics, London, Ontario, Canada.

London Regional Cancer Program, Baines Imaging Research Laboratory, London, Ontario, Canada.

出版信息

J Med Imaging (Bellingham). 2022 Nov;9(6):066001. doi: 10.1117/1.JMI.9.6.066001. Epub 2022 Nov 8.

DOI:10.1117/1.JMI.9.6.066001
PMID:36388142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9641263/
Abstract

PURPOSE

We developed a model integrating multimodal quantitative imaging features from tumor and nontumor regions, qualitative features, and clinical data to improve the risk stratification of patients with resectable non-small cell lung cancer (NSCLC).

APPROACH

We retrospectively analyzed 135 patients [mean age, 69 years (43 to 87, range); 100 male patients and 35 female patients] with NSCLC who underwent upfront surgical resection between 2008 and 2012. The tumor and peritumoral regions on both preoperative CT and FDG PET-CT and the vertebral bodies L3 to L5 on FDG PET were segmented to assess the tumor and bone marrow uptake, respectively. Radiomic features were extracted and combined with clinical and CT qualitative features. A random survival forest model was developed using the top-performing features to predict the time to recurrence/progression in the training cohort ( ), validated in the testing cohort ( ) using the concordance, and compared with a stage-only model. Patients were stratified into high- and low-risks of recurrence/progression using Kaplan-Meier analysis.

RESULTS

The model, consisting of stage, three wavelet texture features, and three wavelet first-order features, achieved a concordance of 0.78 and 0.76 in the training and testing cohorts, respectively, significantly outperforming the baseline stage-only model results of 0.67 ( ) and 0.60 ( ), respectively. Patients at high- and low-risks of recurrence/progression were significantly stratified in both the training ( ) and the testing ( ) cohorts.

CONCLUSIONS

Our radiomic model, consisting of stage and tumor, peritumoral, and bone marrow features from CT and FDG PET-CT significantly stratified patients into low- and high-risk of recurrence/progression.

摘要

目的

我们开发了一种整合肿瘤和非肿瘤区域的多模态定量成像特征、定性特征及临床数据的模型,以改善可切除非小细胞肺癌(NSCLC)患者的风险分层。

方法

我们回顾性分析了2008年至2012年间接受 upfront 手术切除的135例NSCLC患者[平均年龄69岁(43至87岁,范围);男性患者100例,女性患者35例]。对术前CT和FDG PET-CT上的肿瘤及瘤周区域以及FDG PET上的L3至L5椎体进行分割,分别评估肿瘤和骨髓摄取情况。提取放射组学特征,并将其与临床和CT定性特征相结合。使用表现最佳的特征开发随机生存森林模型,以预测训练队列中的复发/进展时间( ),在测试队列( )中使用一致性进行验证,并与仅基于分期的模型进行比较。使用Kaplan-Meier分析将患者分层为复发/进展的高风险和低风险。

结果

该模型由分期、三个小波纹理特征和三个小波一阶特征组成,在训练队列和测试队列中的一致性分别为0.78和0.76,显著优于仅基于分期的基线模型结果,分别为0.67( )和0.60( )。复发/进展高风险和低风险的患者在训练队列( )和测试队列( )中均有显著分层。

结论

我们的放射组学模型由分期以及来自CT和FDG PET-CT的肿瘤、瘤周和骨髓特征组成,可将患者显著分层为复发/进展的低风险和高风险。