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基于 MRI 的放射组学预测同步放化疗治疗局部晚期宫颈鳞癌患者生存价值

MRI-based radiomics value for predicting the survival of patients with locally advanced cervical squamous cell cancer treated with concurrent chemoradiotherapy.

机构信息

Department of Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.

GE Healthcare, MR Research, Beijing, China.

出版信息

Cancer Imaging. 2022 Jul 16;22(1):35. doi: 10.1186/s40644-022-00474-2.

DOI:10.1186/s40644-022-00474-2
PMID:35842679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9287951/
Abstract

BACKGROUND

To investigate the magnetic resonance imaging (MRI)-based radiomics value in predicting the survival of patients with locally advanced cervical squamous cell cancer (LACSC) treated with concurrent chemoradiotherapy (CCRT).

METHODS

A total of 185 patients (training group: n = 128; testing group: n = 57) with LACSC treated with CCRT between January 2014 and December 2018 were retrospectively enrolled in this study. A total of 400 radiomics features were extracted from T2-weighted imaging, apparent diffusion coefficient map, arterial- and delayed-phase contrast-enhanced MRI. Univariate Cox regression and least absolute shrinkage and selection operator Cox regression was applied to select radiomics features and clinical characteristics that could independently predict progression-free survival (PFS) and overall survival (OS). The predictive capability of the prediction model was evaluated using Harrell's C-index. Nomograms and calibration curves were then generated. Survival curves were generated using the Kaplan-Meier method, and the log-rank test was used for comparison.

RESULTS

The radiomics score achieved significantly better predictive performance for the estimation of PFS (C-index, 0.764 for training and 0.762 for testing) and OS (C-index, 0.793 for training and 0.750 for testing), compared with the 2018 FIGO staging system (C-index for PFS, 0.657 for training and 0.677 for testing; C-index for OS, 0.665 for training and 0.633 for testing) and clinical-predicting model (C-index for PFS, 0.731 for training and 0.725 for testing; C-index for OS, 0.708 for training and 0.693 for testing) (P < 0.05). The combined model constructed with T stage, lymph node metastasis position, and radiomics score achieved the best performance for the estimation of PFS (C-index, 0.792 for training and 0.809 for testing) and OS (C-index, 0.822 for training and 0.785 for testing), which were significantly higher than those of the radiomics score (P < 0.05).

CONCLUSIONS

The MRI-based radiomics score could provide effective information in predicting the PFS and OS in patients with LACSC treated with CCRT. The combined model (including MRI-based radiomics score and clinical characteristics) showed the best prediction performance.

摘要

背景

为了探讨磁共振成像(MRI)基于放射组学在预测接受同期放化疗(CCRT)治疗的局部晚期宫颈鳞状细胞癌(LACSC)患者生存中的价值。

方法

本研究回顾性纳入了 2014 年 1 月至 2018 年 12 月期间接受 CCRT 治疗的 185 例 LACSC 患者(训练组:n=128;测试组:n=57)。从 T2 加权成像、表观扩散系数图、动脉期和延迟期对比增强 MRI 中提取了总共 400 个放射组学特征。采用单因素 Cox 回归和最小绝对收缩和选择算子 Cox 回归来选择能够独立预测无进展生存期(PFS)和总生存期(OS)的放射组学特征和临床特征。采用 Harrell's C 指数评估预测模型的预测能力。然后生成列线图和校准曲线。使用 Kaplan-Meier 方法生成生存曲线,并使用对数秩检验进行比较。

结果

放射组学评分在预测 PFS(C 指数,训练组为 0.764,测试组为 0.762)和 OS(C 指数,训练组为 0.793,测试组为 0.750)方面的表现明显优于 2018 年 FIGO 分期系统(PFS 的 C 指数,训练组为 0.657,测试组为 0.677;OS 的 C 指数,训练组为 0.665,测试组为 0.633)和临床预测模型(PFS 的 C 指数,训练组为 0.731,测试组为 0.725;OS 的 C 指数,训练组为 0.708,测试组为 0.693)(P<0.05)。由 T 分期、淋巴结转移位置和放射组学评分构建的联合模型在预测 PFS(C 指数,训练组为 0.792,测试组为 0.809)和 OS(C 指数,训练组为 0.822,测试组为 0.785)方面的表现最佳,明显高于放射组学评分(P<0.05)。

结论

MRI 基于放射组学评分可为接受 CCRT 治疗的 LACSC 患者的 PFS 和 OS 预测提供有效信息。联合模型(包括 MRI 基于放射组学评分和临床特征)显示出最佳的预测性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/f28e75da632e/40644_2022_474_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/ff974ab0666b/40644_2022_474_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/56b8a07a9566/40644_2022_474_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/0c82a7c77092/40644_2022_474_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/e6baa4d1d82c/40644_2022_474_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/f28e75da632e/40644_2022_474_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/ff974ab0666b/40644_2022_474_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/56b8a07a9566/40644_2022_474_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/0c82a7c77092/40644_2022_474_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/e6baa4d1d82c/40644_2022_474_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e180/9287951/f28e75da632e/40644_2022_474_Fig5_HTML.jpg

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