利用靶向临床基因组测序数据进行肿瘤类型预测的深度学习模型。

IF 29.7 1区 医学 Q1 ONCOLOGY Cancer discovery Pub Date : 2024-06-03 DOI:10.1158/2159-8290.CD-23-0996
Madison Darmofal, Shalabh Suman, Gurnit Atwal, Michael Toomey, Jie-Fu Chen, Jason C Chang, Efsevia Vakiani, Anna M Varghese, Anoop Balakrishnan Rema, Aijazuddin Syed, Nikolaus Schultz, Michael F Berger, Quaid Morris
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引用次数: 0

摘要

肿瘤类型可指导癌症的临床治疗决策,但基于组织学的诊断仍具有挑战性。基因组改变对肿瘤类型有很高的诊断价值,根据基因组特征训练的肿瘤类型分类器已经得到了探索,但最准确的方法在临床上并不可行,因为这些方法依赖于从全基因组测序(WGS)中获得的特征,或在有限的癌症类型中进行预测。我们利用来自39,787个实体瘤数据集的基因组特征,使用临床靶向癌症基因面板进行测序,开发出基因组衍生诊断组合(GDD-ES):一种使用深度神经网络进行肿瘤类型分类的超参数组合。GDD-ENS 对 38 种癌症类型的高置信度预测准确率达到 93%,可与基于 WGS 的方法相媲美。GDD-ENS 还能指导罕见类型和原发灶不明癌症的诊断,并结合患者特定的临床信息改进预测。总之,将 GDD-ENS 整合到前瞻性临床测序工作流程中,可以提供与临床相关的肿瘤类型预测,实时指导治疗决策。
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Deep-Learning Model for Tumor-Type Prediction Using Targeted Clinical Genomic Sequencing Data.

Tumor type guides clinical treatment decisions in cancer, but histology-based diagnosis remains challenging. Genomic alterations are highly diagnostic of tumor type, and tumor-type classifiers trained on genomic features have been explored, but the most accurate methods are not clinically feasible, relying on features derived from whole-genome sequencing (WGS), or predicting across limited cancer types. We use genomic features from a data set of 39,787 solid tumors sequenced using a clinically targeted cancer gene panel to develop Genome-Derived-Diagnosis Ensemble (GDD-ENS): a hyperparameter ensemble for classifying tumor type using deep neural networks. GDD-ENS achieves 93% accuracy for high-confidence predictions across 38 cancer types, rivaling the performance of WGS-based methods. GDD-ENS can also guide diagnoses of rare type and cancers of unknown primary and incorporate patient-specific clinical information for improved predictions. Overall, integrating GDD-ENS into prospective clinical sequencing workflows could provide clinically relevant tumor-type predictions to guide treatment decisions in real time.

Significance: We describe a highly accurate tumor-type prediction model, designed specifically for clinical implementation. Our model relies only on widely used cancer gene panel sequencing data, predicts across 38 distinct cancer types, and supports integration of patient-specific nongenomic information for enhanced decision support in challenging diagnostic situations. See related commentary by Garg, p. 906. This article is featured in Selected Articles from This Issue, p. 897.

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来源期刊
Cancer discovery
Cancer discovery ONCOLOGY-
CiteScore
22.90
自引率
1.40%
发文量
838
审稿时长
6-12 weeks
期刊介绍: Cancer Discovery publishes high-impact, peer-reviewed articles detailing significant advances in both research and clinical trials. Serving as a premier cancer information resource, the journal also features Review Articles, Perspectives, Commentaries, News stories, and Research Watch summaries to keep readers abreast of the latest findings in the field. Covering a wide range of topics, from laboratory research to clinical trials and epidemiologic studies, Cancer Discovery spans the entire spectrum of cancer research and medicine.
期刊最新文献
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