对前列腺癌全切片格里森分级进行新评估,以确定根治性前列腺切除术的候选者:一项基于机器学习的多组学研究。

IF 12.4 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Theranostics Pub Date : 2024-08-01 eCollection Date: 2024-01-01 DOI:10.7150/thno.96921
Jing Ning, Clemens P Spielvogel, David Haberl, Karolina Trachtova, Stefan Stoiber, Sazan Rasul, Vojtech Bystry, Gabriel Wasinger, Pascal Baltzer, Elisabeth Gurnhofer, Gerald Timelthaler, Michaela Schlederer, Laszlo Papp, Helga Schachner, Thomas Helbich, Markus Hartenbach, Bernhard Grubmüller, Shahrokh F Shariat, Marcus Hacker, Alexander Haug, Lukas Kenner
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引用次数: 0

摘要

目的:本研究旨在使用多组学机器学习(ML)模型准确评估前列腺癌(PCa)的全切片格里森分级(GG),并将其性能与活检证实的 GG(bxGG)评估进行比较。材料与方法:本侧研究回顾性纳入了前瞻性临床试验(NCT02659527)试点研究中招募的146名PCa患者,他们均在2014年5月至2020年4月期间接受了根治性前列腺切除术(RP)前的68Ga-PSMA-11综合正电子发射断层扫描(PET)/磁共振(MR)检查。为了建立多组学 ML 模型,我们量化了 PET 放射组学特征、全外显子组测序得出的通路级基因组学特征以及 11 种生物标记物免疫组化染色得出的病理组学特征。基于多组学数据集,我们建立了五个 ML 模型,并使用 100 倍蒙特卡洛交叉验证进行了验证。结果显示在五个 ML 模型中,随机森林(RF)模型的曲线下面积(AUC)表现最佳。与单独的 bxGG 评估相比,RF 模型在 AUC(0.87 vs 0.75)、特异性(0.72 vs 0.61)、阳性预测值(0.79 vs 0.75)和准确性(0.78 vs 0.77)方面更胜一筹,而灵敏度(0.83 vs 0.89)和阴性预测值(0.80 vs 0.81)则略有下降。在各类特征中,bxGG 被认为是最重要的特征,其次是病理组学特征、临床特征、放射组学特征和基因组学特征。三个重要的个体特征是 bxGG、PSA 染色和一个与强度相关的放射组学特征。结论研究结果表明,与目前的 bxGG 临床基线相比,所开发的基于多组学的 ML 模型可对全图 GG 进行更优越的评估。这样就能通过识别需要进行 RP 的高风险 PCa 患者,实现个性化的患者管理。
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A novel assessment of whole-mount Gleason grading in prostate cancer to identify candidates for radical prostatectomy: a machine learning-based multiomics study.

Purpose: This study aims to assess whole-mount Gleason grading (GG) in prostate cancer (PCa) accurately using a multiomics machine learning (ML) model and to compare its performance with biopsy-proven GG (bxGG) assessment. Materials and Methods: A total of 146 patients with PCa recruited in a pilot study of a prospective clinical trial (NCT02659527) were retrospectively included in the side study, all of whom underwent 68Ga-PSMA-11 integrated positron emission tomography (PET) / magnetic resonance (MR) before radical prostatectomy (RP) between May 2014 and April 2020. To establish a multiomics ML model, we quantified PET radiomics features, pathway-level genomics features from whole exome sequencing, and pathomics features derived from immunohistochemical staining of 11 biomarkers. Based on the multiomics dataset, five ML models were established and validated using 100-fold Monte Carlo cross-validation. Results: Among five ML models, the random forest (RF) model performed best in terms of the area under the curve (AUC). Compared to bxGG assessment alone, the RF model was superior in terms of AUC (0.87 vs 0.75), specificity (0.72 vs 0.61), positive predictive value (0.79 vs 0.75), and accuracy (0.78 vs 0.77) and showed slightly decreased sensitivity (0.83 vs 0.89) and negative predictive value (0.80 vs 0.81). Among the feature categories, bxGG was identified as the most important feature, followed by pathomics, clinical, radiomics and genomics features. The three important individual features were bxGG, PSA staining and one intensity-related radiomics feature. Conclusion: The findings demonstrate a superior assessment of the developed multiomics-based ML model in whole-mount GG compared to the current clinical baseline of bxGG. This enables personalized patient management by identifying high-risk PCa patients for RP.

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来源期刊
Theranostics
Theranostics MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
25.40
自引率
1.60%
发文量
433
审稿时长
1 months
期刊介绍: Theranostics serves as a pivotal platform for the exchange of clinical and scientific insights within the diagnostic and therapeutic molecular and nanomedicine community, along with allied professions engaged in integrating molecular imaging and therapy. As a multidisciplinary journal, Theranostics showcases innovative research articles spanning fields such as in vitro diagnostics and prognostics, in vivo molecular imaging, molecular therapeutics, image-guided therapy, biosensor technology, nanobiosensors, bioelectronics, system biology, translational medicine, point-of-care applications, and personalized medicine. Encouraging a broad spectrum of biomedical research with potential theranostic applications, the journal rigorously peer-reviews primary research, alongside publishing reviews, news, and commentary that aim to bridge the gap between the laboratory, clinic, and biotechnology industries.
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