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超声图像的放射组学分析用于鉴别超声检查中具有实性形态的附件区良恶性肿块。

Radiomics analysis of ultrasound images to discriminate between benign and malignant adnexal masses with solid morphology on ultrasound.

作者信息

Moro F, Vagni M, Tran H E, Bernardini F, Mascilini F, Ciccarone F, Nero C, Giannarelli D, Boldrini L, Fagotti A, Scambia G, Valentin L, Testa A C

机构信息

Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Istituto di Radiologia, Università Cattolica del Sacro Cuore, Rome, Italy.

出版信息

Ultrasound Obstet Gynecol. 2025 Mar;65(3):353-363. doi: 10.1002/uog.27680. Epub 2025 Feb 2.

DOI:10.1002/uog.27680
PMID:38748935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11872347/
Abstract

OBJECTIVE

The primary aim was to identify radiomics ultrasound features that can distinguish between benign and malignant adnexal masses with solid ultrasound morphology, and between primary malignant (including borderline and primary invasive) and metastatic solid ovarian masses, and to develop ultrasound-based machine learning models that include radiomics features to discriminate between benign and malignant solid adnexal masses. The secondary aim was to compare the discrimination performance of our newly developed radiomics models with that of the Assessment of Different NEoplasias in the adneXa (ADNEX) model and that of subjective assessment by an experienced ultrasound examiner.

METHODS

This was a retrospective, observational single-center study conducted at Fondazione Policlinico Universitario A. Gemelli IRCC, in Rome, Italy. Included were patients with a histological diagnosis of an adnexal tumor with solid morphology according to International Ovarian Tumor Analysis (IOTA) terminology at preoperative ultrasound examination performed in 2014-2020, who were managed with surgery. The patient cohort was split randomly into training and validation sets at a ratio of 70:30 and with the same proportion of benign and malignant tumors in the two subsets, with malignant tumors including borderline, primary invasive and metastatic tumors. We extracted 68 radiomics features, belonging to two different families: intensity-based statistical features and textural features. Models to predict malignancy were built based on a random forest classifier, fine-tuned using 5-fold cross-validation over the training set, and tested on the held-out validation set. The variables used in model-building were patient age and radiomics features that were statistically significantly different between benign and malignant adnexal masses and assessed as not redundant based on the Pearson correlation coefficient. We evaluated the discriminative ability of the models and compared it to that of the ADNEX model and that of subjective assessment by an experienced ultrasound examiner using the area under the receiver-operating-characteristics curve (AUC) and classification performance by calculating sensitivity and specificity.

RESULTS

In total, 326 patients were included and 775 preoperative ultrasound images were analyzed. Of the 68 radiomics features extracted, 52 differed statistically significantly between benign and malignant tumors in the training set, and 18 uncorrelated features were selected for inclusion in model-building. The same 52 radiomics features differed significantly between benign, primary malignant and metastatic tumors. However, the values of the features manifested overlapped between primary malignant and metastatic tumors and did not differ significantly between them. In the validation set, 25/98 (25.5%) tumors were benign and 73/98 (74.5%) were malignant (6 borderline, 57 primary invasive, 10 metastatic). In the validation set, a model including only radiomics features had an AUC of 0.80, sensitivity of 0.78 and specificity of 0.76 at an optimal cut-off for risk of malignancy of 68%, based on Youden's index. The corresponding results for a model including age and radiomics features were AUC of 0.79, sensitivity of 0.86 and specificity of 0.56 (cut-off 60%, based on Youden's index), while those of the ADNEX model were AUC of 0.88, sensitivity of 0.99 and specificity of 0.64 (at a 20% risk-of-malignancy cut-off). Subjective assessment had a sensitivity of 0.99 and specificity of 0.72.

CONCLUSIONS

Our radiomics model had moderate discriminative ability on internal validation and the addition of age to this model did not improve its performance. Even though our radiomics models had discriminative ability inferior to that of the ADNEX model, our results are sufficiently promising to justify continued development of radiomics analysis of ultrasound images of adnexal masses. © 2024 The Author(s). Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

摘要

目的

主要目的是识别能够区分具有实性超声形态的良性和恶性附件肿块,以及原发性恶性(包括交界性和原发性浸润性)和转移性实性卵巢肿块的放射组学超声特征,并开发基于超声的机器学习模型,该模型包含放射组学特征以区分良性和恶性实性附件肿块。次要目的是将我们新开发的放射组学模型的鉴别性能与附件不同肿瘤评估(ADNEX)模型以及经验丰富的超声检查者的主观评估的鉴别性能进行比较。

方法

这是一项在意大利罗马的圣心天主教大学综合医院基金会IRCC进行的回顾性、观察性单中心研究。纳入的患者在2014 - 2020年术前超声检查时根据国际卵巢肿瘤分析(IOTA)术语具有组织学诊断为实性形态的附件肿瘤,并接受了手术治疗。患者队列以70:30的比例随机分为训练集和验证集,且两个子集中良性和恶性肿瘤的比例相同,恶性肿瘤包括交界性、原发性浸润性和转移性肿瘤。我们提取了68个放射组学特征,属于两个不同的类别:基于强度的统计特征和纹理特征。基于随机森林分类器构建预测恶性肿瘤的模型,在训练集上使用5折交叉验证进行微调,并在留出的验证集上进行测试。模型构建中使用的变量是患者年龄以及在良性和恶性附件肿块之间有统计学显著差异且根据皮尔逊相关系数评估为非冗余的放射组学特征。我们评估了模型的鉴别能力,并使用受试者工作特征曲线下面积(AUC)以及通过计算敏感性和特异性来比较其与ADNEX模型以及经验丰富的超声检查者的主观评估的鉴别能力。

结果

总共纳入了326例患者,分析了775张术前超声图像。在提取的68个放射组学特征中,训练集中52个在良性和恶性肿瘤之间有统计学显著差异,选择了18个不相关特征纳入模型构建。相同的52个放射组学特征在良性、原发性恶性和转移性肿瘤之间也有显著差异。然而,这些特征的值在原发性恶性和转移性肿瘤之间表现出重叠,且它们之间没有显著差异。在验证集中,98个肿瘤中有25个(25.5%)为良性,73个(74.5%)为恶性(6个交界性,57个原发性浸润性,10个转移性)。在验证集中,仅包含放射组学特征的模型在基于约登指数的恶性风险最佳截断值为68%时,AUC为0.80,敏感性为0.78,特异性为0.76。包含年龄和放射组学特征的模型的相应结果为AUC为0.79,敏感性为0.86,特异性为0.56(基于约登指数的截断值为60%),而ADNEX模型的结果为AUC为0.88,敏感性为0.99,特异性为0.64(在恶性风险截断值为20%时)。主观评估的敏感性为0.99,特异性为0.72。

结论

我们的放射组学模型在内部验证中具有中等鉴别能力,并且在该模型中加入年龄并未改善其性能。尽管我们的放射组学模型的鉴别能力不如ADNEX模型,但我们的结果足以令人鼓舞,证明继续开展附件肿块超声图像的放射组学分析是合理的。© 2024作者。《妇产科超声》由约翰·威利父子有限公司代表国际妇产科超声学会出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8d/11872347/38267332b41f/UOG-65-353-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8d/11872347/1971dd5de845/UOG-65-353-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8d/11872347/efbea23e7550/UOG-65-353-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8d/11872347/38267332b41f/UOG-65-353-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8d/11872347/1971dd5de845/UOG-65-353-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8d/11872347/efbea23e7550/UOG-65-353-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d8d/11872347/38267332b41f/UOG-65-353-g002.jpg

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