乳腺癌化疗的心脏毒性检测工具:一项回顾性研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-02 eCollection Date: 2024-01-01 DOI:10.7717/peerj-cs.2230
Ahmad Alenezi, Fergus McKiddie, Mintu Nath, Ali Mayya, Andy Welch
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引用次数: 0

摘要

背景:接受生物治疗和/或化疗的乳腺癌患者需要进行多次放射性核素血管造影(RNA)或多显像采集(MUGA)扫描,以评估心脏毒性。RNA成像参数与左心室射血分数(LVEF)之间的关系仍不清楚:本研究旨在提取和评估几种新型成像生物标志物与检测化疗中乳腺癌患者左心室射血分数变化之间的关联:我们开发并优化了一套名为 "RNA 工具箱 "的新型 MATLAB 程序,用于从 RNA 图像中提取参数。通过各种统计检验(如方差分析、Bland-Altman 和类内相关检验)对代码进行了优化。我们使用回归模型和接收者操作特征曲线(ROC)对图像进行了定量分析,以确定这些参数之间的关联:结果:代码的可重复性很好,从两个软件包中提取的参数与经过验证的临床软件显示出良好的一致性。回归模型和 ROC 结果在预测 LVEF 方面具有统计学意义(R2 = 0.40,P < 0.001)(AUC = 0.78)。一些基于时间、形状和计数的参数与化疗后LVEF(β = 0.09,P < 0.001)、相位图像的LVEF(β = 4,P = 0.030)、近似熵(ApEn)(β = 11.6,P = 0.001)、ApEn(舒张期和收缩期)(β = 39,P = 0.002)和左心室收缩期大小(β = 0.03,P = 0.010)显著相关:尽管样本量有限,但我们观察到多个参数与 LVEF 之间存在关联。我们相信,这些参数对接受心脏毒性化疗的患者比目前的方法更有益。此外,这种方法还能帮助医生评估化疗期间亚临床心脏变化,了解心脏保护药物的潜在益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiotoxicity detection tool for breast cancer chemotherapy: a retrospective study.

Background: Patients with breast cancer undergoing biological therapy and/or chemotherapy perform multiple radionuclide angiography (RNA) or multigated acquisition (MUGA) scans to assess cardiotoxicity. The association between RNA imaging parameters and left ventricular (LV) ejection fraction (LVEF) remains unclear.

Objectives: This study aimed to extract and evaluate the association of several novel imaging biomarkers to detect changes in LVEF in patients with breast cancer undergoing chemotherapy.

Methods: We developed and optimized a novel set of MATLAB routines called the "RNA Toolbox" to extract parameters from RNA images. The code was optimized using various statistical tests (e.g., ANOVA, Bland-Altman, and intraclass correlation tests). We quantitatively analyzed the images to determine the association between these parameters using regression models and receiver operating characteristic (ROC) curves.

Results: The code was reproducible and showed good agreement with validated clinical software for the parameters extracted from both packages. The regression model and ROC results were statistically significant in predicting LVEF (R2 = 0.40, P < 0.001) (AUC = 0.78). Some time-based, shape-based, and count-based parameters were significantly associated with post-chemotherapy LVEF (β = 0.09, P < 0.001), LVEF of phase image (β = 4, P = 0.030), approximate entropy (ApEn) (β = 11.6, P = 0.001), ApEn (diastolic and systolic) (β = 39, P = 0.002) and LV systole size (β = 0.03, P = 0.010).

Conclusions: Despite the limited sample size, we observed evidence of associations between several parameters and LVEF. We believe that these parameters will be more beneficial than the current methods for patients undergoing cardiotoxic chemotherapy. Moreover, this approach can aid physicians in evaluating subclinical cardiac changes during chemotherapy, and in understanding the potential benefits of cardioprotective drugs.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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