放射组学检测三阴性乳腺癌化生组织学:迈向个体化治疗的一步。

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Rana Gunoz Comert, Gorkem Durak, Ravza Yilmaz, Halil Ertugrul Aktas, Zeynep Tuz, Hongyi Pan, Jun Zeng, Aysel Bayram, Baran Mollavelioglu, Sukru Mehmet Erturk, Ulas Bagci
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引用次数: 0

摘要

本研究旨在开发和验证基于多序列mri的放射组学方法,用于在初始诊断时区分化生性乳腺癌(MBC)和非化生性三阴性乳腺癌(TNBC),从而促进最佳治疗选择。在这项回顾性研究中,我们分析了105例患者(27例MBC, 78例非化生TNBC),他们接受了标准化的乳房磁共振成像(MRI),包括t1加权对比增强(T1W-CE)和短tau反转恢复(STIR)序列。两名放射科医生进行了真实病灶分割,由一名高级放射科医生验证。我们提取了214个放射学特征(使用PyRadiomics),并使用最小绝对收缩和选择算子(LASSO)回归进行特征选择。使用五倍交叉验证对七个机器学习分类器进行了全面评估,并通过ROC分析和准确性指标评估了性能。T1W- ce和STIR联合分析在区分MBC和非化生TNBC方面具有更好的诊断效果(AUC = 0.845,准确度= 81%),而单独使用任何一种序列(T1W仅AUC = 0.805,准确度= 80%;STIR仅AUC:0.768,准确度= 77%)。多序列MRI放射组学可以在初始诊断时可靠地区分MBC和TNBC。这可能有助于选择更合适的治疗方法,并有助于避免对MBC患者无效的化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiomics for Detecting Metaplastic Histology in Triple-Negative Breast Cancer: A Step Towards Personalized Therapy.

This study aims to develop and validate a multisequence MRI-based radiomics approach for distinguishing metaplastic breast cancer (MBC) from non-metaplastic triple-negative breast cancer (TNBC) at the initial diagnosis, which could facilitate optimal treatment selection. In this retrospective study, we analyzed 105 patients (27 MBC, 78 non-metaplastic TNBC) who underwent standardized breast magnetic resonance imaging (MRI), which included T1-weighted contrast-enhanced (T1W-CE) and short-tau inversion recovery (STIR) sequences. Two radiologists performed ground truth lesion segmentation, verified by a senior radiologist. We extracted 214 radiomic features (using PyRadiomics) and used least absolute shrinkage and selection operator (LASSO) regression for feature selection. Seven machine learning classifiers were thoroughly evaluated using five-fold cross-validation, with performance assessed through ROC analysis and accuracy metrics. The combined T1W-CE and STIR analysis demonstrated superior diagnostic performance for distinguishing MBC from non-metaplastic TNBC (AUC = 0.845; accuracy = 81%) compared with either sequence alone (T1W only AUC = 0.805; accuracy = 80%; STIR only AUC:0.768; accuracy = 77%). Multisequence MRI radiomics can reliably distinguish between MBC and TNBC at the time of initial diagnosis. This could potentially facilitate the selection of more appropriate treatments and help avoid ineffective chemotherapy for MBC patients.

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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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