Magnetic resonance imaging-based radiomics in predicting the expression of Ki-67, p53, and epidermal growth factor receptor in rectal cancer.

IF 2 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of gastrointestinal oncology Pub Date : 2024-10-31 Epub Date: 2024-10-29 DOI:10.21037/jgo-24-220
Qiying Li, Jinkai Liu, Weneng Li, Mingzhu Qiu, Xiaohua Zhuo, Qikui You, Shaohua Qiu, Qi Lin, Yi Liu
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Abstract

Background: The preoperative evaluation of the expression levels of Ki-67, p53, and epidermal growth factor receptor (EGFR) based on magnetic resonance imaging (MRI) of rectal cancer is necessary to facilitate individualized therapy. This study aimed to develop and validate radiomics models for the evaluation of the expression levels of Ki-67, p53, and EGFR of rectal cancer from preoperative MRI.

Methods: In this retrospective study, 124 patients (38 in the test group and 86 in the training group) with rectal cancer who underwent preoperative MRI and postoperative Ki-67, p53 and EGFR assay were included in Longyan First Affiliated Hospital of Fujian Medical University from June 2015 to October 2019. A total of 796 radiomics features were acquired from both diffusion-weighted imaging (DWI) and T2-weighted imaging (T2WI). Least absolute shrinkage and selection operator (LASSO) and the minimum redundancy maximum relevance (mRMR) were used to select the most predictive texture features, and then the radiomics score (Rad-score) models were derived to evaluate Ki-67, p53, and EGFR expression status based on the radiomics signature. The receiver operating characteristic (ROC) was used to assess the model's performance, and the reliability was verified via accuracy, sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV).

Results: The Rad-score evaluation of Ki-67 expression status yielded area under the curve (AUC) values of 0.91 [95% confidence interval (CI): 0.87-0.95] and 0.81 (95% CI: 0.66-0.96) in the training and test groups. The evaluation of p53 expression produced AUC values of 0.82 (95% CI: 0.77-0.88) and 0.80 (95% CI: 0.65-0.96). For evaluating EGFR expression status in both training and test groups, the AUC values were 0.86 (95% CI: 0.81-0.91) and 0.76 (95% CI: 0.58-0.93), respectively. While Rad-score of Ki-67 expression status in the training group obtained the top accuracy, sensitivity, specificity, and PPV with values of 0.85, 0.80, 0.92, and 0.93.

Conclusions: Preoperative MRI-based radiomics analysis has the ability to noninvasively assess the postoperative Ki-67, p53, and EGFR of rectal cancer.

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基于磁共振成像的放射组学预测直肠癌中 Ki-67、p53 和表皮生长因子受体的表达。
背景:基于直肠癌磁共振成像(MRI)对Ki-67、p53和表皮生长因子受体(EGFR)的表达水平进行术前评估对于促进个体化治疗非常必要。本研究旨在开发和验证放射组学模型,以评估直肠癌术前磁共振成像中 Ki-67、p53 和表皮生长因子受体的表达水平:在这项回顾性研究中,纳入了2015年6月至2019年10月在福建医科大学附属龙岩第一医院接受术前MRI和术后Ki-67、p53和EGFR检测的124例直肠癌患者(试验组38例,训练组86例)。弥散加权成像(DWI)和T2加权成像(T2WI)共获得796个放射组学特征。利用最小绝对收缩和选择算子(LASSO)和最小冗余最大相关性(mRMR)来选择最具预测性的纹理特征,然后得出放射组学评分(Rad-score)模型,根据放射组学特征来评估Ki-67、p53和表皮生长因子受体(EGFR)的表达状态。使用接收器操作特征(ROC)评估模型的性能,并通过准确性、灵敏度、特异性、阳性预测值(PPV)和阴性预测值(NPV)验证其可靠性:对 Ki-67 表达状态进行 Rad-score 评估后,训练组和测试组的曲线下面积(AUC)值分别为 0.91 [95% 置信区间 (CI):0.87-0.95] 和 0.81 (95% CI:0.66-0.96)。p53 表达评估的 AUC 值分别为 0.82(95% CI:0.77-0.88)和 0.80(95% CI:0.65-0.96)。在评估训练组和测试组的表皮生长因子受体表达状态时,AUC 值分别为 0.86(95% CI:0.81-0.91)和 0.76(95% CI:0.58-0.93)。而训练组的Ki-67表达状态Rad-score的准确性、灵敏度、特异性和PPV值分别为0.85、0.80、0.92和0.93,均名列前茅:基于术前磁共振成像的放射组学分析能够无创评估直肠癌术后Ki-67、p53和表皮生长因子受体(EGFR)的情况。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
171
期刊介绍: ournal of Gastrointestinal Oncology (Print ISSN 2078-6891; Online ISSN 2219-679X; J Gastrointest Oncol; JGO), the official journal of Society for Gastrointestinal Oncology (SGO), is an open-access, international peer-reviewed journal. It is published quarterly (Sep. 2010- Dec. 2013), bimonthly (Feb. 2014 -) and openly distributed worldwide. JGO publishes manuscripts that focus on updated and practical information about diagnosis, prevention and clinical investigations of gastrointestinal cancer treatment. Specific areas of interest include, but not limited to, multimodality therapy, markers, imaging and tumor biology.
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