Abstract 4517: Comprehensive intraoperative imaging of surgical margins with AI-driven open-top light-sheet microscopy

IF 12.5 1区 医学 Q1 ONCOLOGY
David Brenes, Qinghua Han, Rui Wang, Rauf Kareem, Michael C. Topf, Eben L. Rosenthal, Emily Marchiano, Emily Palmquist, Faisal Mahmood, Sara H. Javid, Suzanne M. Dintzis, Jonathan T. Liu
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引用次数: 0

Abstract

Surgeons rely on subjective visual and tactile feedback to differentiate tumors from adjacent normal tissue, which lacks accuracy and may make complete resection challenging. Over 20% of breast and 40% of head & neck cancer surgeries yield positive margins—cancerous cells at the edge of the resected specimen—requiring costly additional treatments with inferior outcomes. When pathologists assess margins, they quantify the tumor's proximity to the margin surface, where a margin of several millimeters is often desired. This is done by viewing formalin-fixed, paraffin-embedded (FFPE) tissue sections oriented perpendicularly to the specimen surface. FFPE sections are typically ∼5 µm thick and are obtained at 3 - 5 mm intervals, meaning that < 0.1% of the specimen surface is evaluated. We propose that for solid continuous tumors, comprehensive surface microscopy — though unable to measure the tumor’s proximity to the specimen surface — could more accurately identify positive margins and could be performed rapidly in the operating room to maintain specimen orientation. We are developing an intraoperative open-top light-sheet (OTLS) microscopy system that comprehensively assesses fresh specimen surfaces through an artificial intelligence (AI)-driven, time-efficient, multi-resolution workflow. The system resembles a flatbed scanner and images the bottom face of a specimen placed on a glass plate. Fresh specimens are rapidly stained (< 1 min) with a fluorescent agent for nuclear and stromal contrast. A profilometer quickly (< 1 min) obtains a height map of the specimen’s bottom surface to guide the OTLS microscope as it captures a thin volume (50 – 100 µm in depth) encompassing the specimen’s surface. The OTLS microscope operates at two resolution modes: low (∼5 × 5 × 5 µm xyz) and high (∼1 × 1 × 3 µm xyz). First, a comprehensive low-resolution scan is acquired rapidly (< 3 min per 10 x 10 cm area). An AI model then identifies high-risk regions to re-scan at high resolution for diagnosis. Our 3D AI-driven imaging strategy mimics the time-efficient workflow of pathologists, who first examine FFPE slides at low magnification before zooming into localized regions at high magnification. The ability to acquire a shallow amount of volumetric data (up to ∼ 100 microns deep) can improve positive margin detection over a single 2D surface due to the greater amount of cellular information and the ability to avoid artifacts from surgical damage (e.g. cautery). To develop our 3D AI algorithm, we are building a dataset from freshly excised breast and head & neck specimens, with ground-truth diagnostic labels provided by pathologists. The model will be weakly supervised, using pre-trained models for 3D feature extraction.In summary, AI-guided multi-resolution OTLS microscopy has the potential to enable rapid, comprehensive intraoperative margin assessment, reducing positive margin rates and improving patient outcomes. Citation Format: David Brenes, Qinghua Han, Rui Wang, Rauf Kareem, Michael C. Topf, Eben L. Rosenthal, Emily Marchiano, Emily Palmquist, Faisal Mahmood, Sara H. Javid, Suzanne M. Dintzis, Jonathan T. Liu. Comprehensive intraoperative imaging of surgical margins with AI-driven open-top light-sheet microscopy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular s); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1): nr 4517.
摘要:人工智能驱动的开顶薄片显微镜术中手术边缘的综合成像
外科医生依靠主观的视觉和触觉反馈来区分肿瘤与邻近的正常组织,这缺乏准确性,并且可能使完全切除具有挑战性。超过20%的乳房和40%的头部颈部癌症手术产生阳性边缘-切除标本边缘的癌细胞-需要昂贵的额外治疗,效果较差。当病理学家评估边缘时,他们量化肿瘤与边缘表面的接近程度,通常需要几毫米的边缘。这是通过观察福尔马林固定,石蜡包埋(FFPE)组织切片垂直于标本表面来完成的。FFPE切片通常厚约5µm,间隔3 - 5mm,这意味着&;lt;0.1%的试样表面被评估。我们建议,对于实体连续肿瘤,综合表面显微镜虽然无法测量肿瘤与标本表面的接近程度,但可以更准确地识别阳性边缘,并且可以在手术室快速进行以保持标本方向。我们正在开发一种术中开顶光片(OTLS)显微镜系统,该系统通过人工智能(AI)驱动、高效、多分辨率的工作流程全面评估新鲜标本表面。该系统类似于平板扫描仪,对放置在玻璃板上的标本的底面进行成像。新鲜标本快速染色(<;1分钟)用荧光剂对核和间质进行对比。轮廓仪快速(<;(1分钟)获得样品底表面的高度图,以指导OTLS显微镜捕获包含样品表面的薄体积(50 - 100 μ m深度)。OTLS显微镜在两种分辨率模式下工作:低(~ 5 × 5 × 5µm xyz)和高(~ 1 × 1 × 3µm xyz)。首先,快速获得全面的低分辨率扫描(<;每10 × 10厘米面积3分钟)。然后,人工智能模型识别高风险区域,以高分辨率重新扫描以进行诊断。我们的3D人工智能驱动成像策略模仿了病理学家的高效工作流程,他们首先在低倍率下检查FFPE切片,然后在高倍率下放大到局部区域。由于获得更大量的细胞信息和避免手术损伤(例如烧灼)造成的伪影的能力,获得浅层体积数据(高达~ 100微米深)的能力可以改善单个2D表面上的正边缘检测。为了开发我们的3D人工智能算法,我们正在从刚切除的乳房和头部建立一个数据集。颈部标本,病理学家提供的诊断标签。模型将被弱监督,使用预训练模型进行3D特征提取。总之,人工智能引导的多分辨率OTLS显微镜有可能实现快速、全面的术中切缘评估,降低阳性切缘率,改善患者预后。引文格式:David Brenes, Qinghua Han, Rui Wang, Rauf Kareem, Michael C. Topf, Eben L. Rosenthal, Emily Marchiano, Emily Palmquist, Faisal Mahmood, Sara H. Javid, Suzanne M. Dintzis, Jonathan T. Liu人工智能驱动开顶光片显微镜术中手术边缘的综合成像[摘要]。摘自:《2025年美国癌症研究协会年会论文集》;第1部分(常规);2025年4月25日至30日;费城(PA): AACR;中国生物医学工程学报(英文版);2009;31(5):557 - 557。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer research
Cancer research 医学-肿瘤学
CiteScore
16.10
自引率
0.90%
发文量
7677
审稿时长
2.5 months
期刊介绍: Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research. With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445. Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.
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