利用受激拉曼组织学和深度学习术中快速检测原发性中枢神经系统淋巴瘤并与常见的中枢神经系统肿瘤进行鉴别。

IF 16.4 1区 医学 Q1 CLINICAL NEUROLOGY
David Reinecke, Nader Maarouf, Andrew Smith, Daniel Alber, John Markert, Nicolas K Goff, Todd C Hollon, Asadur Chowdury, Cheng Jiang, Xinhai Hou, Anna-Katharina Meissner, Gina Fürtjes, Maximilian I Ruge, Daniel Ruess, Thomas Stehle, Abdulkader Al-Shughri, Lisa I Körner, Georg Widhalm, Thomas Roetzer-Pejrimovsky, John G Golfinos, Matija Snuderl, Volker Neuschmelting, Daniel A Orringer
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引用次数: 0

摘要

背景:准确的术中诊断对于区分原发性中枢神经系统淋巴瘤(PCNSL)和其他中枢神经系统实体至关重要,可为手术决策提供指导,但由于组织形态学特征重叠、时间限制和治疗策略不同,术中诊断面临巨大挑战。我们将受激拉曼组织学(SRH)与深度学习相结合,以应对这一挑战:我们在术中使用便携式拉曼散射显微镜对未经处理的无标记组织样本进行成像,在不到三分钟的时间内生成类似 H&E 的虚拟图像。我们基于自监督学习策略开发了名为 RapidLymphoma 的深度学习管道,用于(1)检测 PCNSL,(2)与其他中枢神经系统实体进行区分,(3)在前瞻性国际多中心队列和另外两个独立测试队列中测试诊断性能。我们对 54,000 张 SRH 补丁图像进行了训练,这些图像来自手术切除和立体定向引导活检,包括各种中枢神经系统肿瘤/非肿瘤病变。训练和测试数据来自四个三级国际医疗中心。最终的组织病理学诊断为基础真相:在 PCNSL 和非 PCNSL 实体的前瞻性测试队列(n=160)中,RapidLymphoma 的总体平衡准确率为 97.81% ±0.91,在检测 PCNSL 方面不逊于冰冻切片分析(100% 对 77.77%)。在区分 IDH 野生型弥漫性胶质瘤和各种脑转移瘤与 PCNSL 方面,额外的测试组群(n=420、n=59)达到了 95.44% ±0.74 和 95.57% ±2.47 的均衡准确率。视觉热图显示了 RapidLymphoma 检测特定类别组织形态学关键特征的能力:结论:RapidLymphoma 在术中检测 PCNSL 并与其他中枢神经系统实体进行鉴别方面证明是可靠有效的。它能在三分钟内提供视觉反馈,从而快速做出临床决策和后续治疗策略规划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fast intraoperative detection of primary CNS lymphoma and differentiation from common CNS tumors using stimulated Raman histology and deep learning.

Background: Accurate intraoperative diagnosis is crucial for differentiating between primary CNS lymphoma (PCNSL) and other CNS entities, guiding surgical decision-making, but represents significant challenges due to overlapping histomorphological features, time constraints, and differing treatment strategies. We combined stimulated Raman histology (SRH) with deep learning to address this challenge.

Methods: We imaged unprocessed, label-free tissue samples intraoperatively using a portable Raman scattering microscope, generating virtual H&E-like images within less than three minutes. We developed a deep learning pipeline called RapidLymphoma based on a self-supervised learning strategy to (1) detect PCNSL, (2) differentiate from other CNS entities, and (3) test the diagnostic performance in a prospective international multicenter cohort and two additional independent test cohorts. We trained on 54,000 SRH patch images sourced from surgical resections and stereotactic-guided biopsies, including various CNS neoplastic/non-neoplastic lesions. Training and test data were collected from four tertiary international medical centers. The final histopathological diagnosis served as ground-truth.

Results: In the prospective test cohort of PCNSL and non-PCNSL entities (n=160), RapidLymphoma achieved an overall balanced accuracy of 97.81% ±0.91, non-inferior to frozen section analysis in detecting PCNSL (100% vs. 77.77%). The additional test cohorts (n=420, n=59) reached balanced accuracy rates of 95.44% ±0.74 and 95.57% ±2.47 in differentiating IDH-wildtype diffuse gliomas and various brain metastasis from PCNSL. Visual heatmaps revealed RapidLymphoma's capabilities to detect class-specific histomorphological key features.

Conclusions: RapidLymphoma proves reliable and valid for intraoperative PCNSL detection and differentiation from other CNS entities. It provides visual feedback within three minutes, enabling fast clinical decision-making and subsequent treatment strategy planning.

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来源期刊
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
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