{"title":"利用深度学习将苏木精-伊红染色转化为 Ki-67 免疫组化数字染色图像:对标记指数的实验验证。","authors":"Cunyuan Ji, Kengo Oshima, Takumi Urata, Fumikazu Kimura, Keiko Ishii, Takeshi Uehara, Kenji Suzuki, Saori Takeyama, Masahiro Yamaguchi","doi":"10.1117/1.JMI.11.4.047501","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Endometrial cancer (EC) is one of the most common types of cancer affecting women. While the hematoxylin-and-eosin (H&E) staining remains the standard for histological analysis, the immunohistochemistry (IHC) method provides molecular-level visualizations. Our study proposes a digital staining method to generate the hematoxylin-3,3'-diaminobenzidine (H-DAB) IHC stain of Ki-67 for the whole slide image of the EC tumor from its H&E stain counterpart.</p><p><strong>Approach: </strong>We employed a color unmixing technique to yield stain density maps from the optical density (OD) of the stains and utilized the U-Net for end-to-end inference. The effectiveness of the proposed method was evaluated using the Pearson correlation between the digital and physical stain's labeling index (LI), a key metric indicating tumor proliferation. Two different cross-validation schemes were designed in our study: intraslide validation and cross-case validation (CCV). In the widely used intraslide scheme, the training and validation sets might include different regions from the same slide. The rigorous CCV validation scheme strictly prohibited any validation slide from contributing to training.</p><p><strong>Results: </strong>The proposed method yielded a high-resolution digital stain with preserved histological features, indicating a reliable correlation with the physical stain in terms of the Ki-67 LI. In the intraslide scheme, using intraslide patches resulted in a biased accuracy (e.g., <math><mrow><mi>R</mi> <mo>=</mo> <mn>0.98</mn></mrow> </math> ) significantly higher than that of CCV. The CCV scheme retained a fair correlation (e.g., <math><mrow><mi>R</mi> <mo>=</mo> <mn>0.66</mn></mrow> </math> ) between the LIs calculated from the digital stain and its physical IHC counterpart. Inferring the OD of the IHC stain from that of the H&E stain enhanced the correlation metric, outperforming that of the baseline model using the RGB space.</p><p><strong>Conclusions: </strong>Our study revealed that molecule-level insights could be obtained from H&E images using deep learning. Furthermore, the improvement brought via OD inference indicated a possible method for creating more generalizable models for digital staining via per-stain analysis.</p>","PeriodicalId":47707,"journal":{"name":"Journal of Medical Imaging","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11287056/pdf/","citationCount":"0","resultStr":"{\"title\":\"Transformation from hematoxylin-and-eosin staining to Ki-67 immunohistochemistry digital staining images using deep learning: experimental validation on the labeling index.\",\"authors\":\"Cunyuan Ji, Kengo Oshima, Takumi Urata, Fumikazu Kimura, Keiko Ishii, Takeshi Uehara, Kenji Suzuki, Saori Takeyama, Masahiro Yamaguchi\",\"doi\":\"10.1117/1.JMI.11.4.047501\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Endometrial cancer (EC) is one of the most common types of cancer affecting women. While the hematoxylin-and-eosin (H&E) staining remains the standard for histological analysis, the immunohistochemistry (IHC) method provides molecular-level visualizations. Our study proposes a digital staining method to generate the hematoxylin-3,3'-diaminobenzidine (H-DAB) IHC stain of Ki-67 for the whole slide image of the EC tumor from its H&E stain counterpart.</p><p><strong>Approach: </strong>We employed a color unmixing technique to yield stain density maps from the optical density (OD) of the stains and utilized the U-Net for end-to-end inference. The effectiveness of the proposed method was evaluated using the Pearson correlation between the digital and physical stain's labeling index (LI), a key metric indicating tumor proliferation. Two different cross-validation schemes were designed in our study: intraslide validation and cross-case validation (CCV). In the widely used intraslide scheme, the training and validation sets might include different regions from the same slide. The rigorous CCV validation scheme strictly prohibited any validation slide from contributing to training.</p><p><strong>Results: </strong>The proposed method yielded a high-resolution digital stain with preserved histological features, indicating a reliable correlation with the physical stain in terms of the Ki-67 LI. In the intraslide scheme, using intraslide patches resulted in a biased accuracy (e.g., <math><mrow><mi>R</mi> <mo>=</mo> <mn>0.98</mn></mrow> </math> ) significantly higher than that of CCV. The CCV scheme retained a fair correlation (e.g., <math><mrow><mi>R</mi> <mo>=</mo> <mn>0.66</mn></mrow> </math> ) between the LIs calculated from the digital stain and its physical IHC counterpart. Inferring the OD of the IHC stain from that of the H&E stain enhanced the correlation metric, outperforming that of the baseline model using the RGB space.</p><p><strong>Conclusions: </strong>Our study revealed that molecule-level insights could be obtained from H&E images using deep learning. 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引用次数: 0
摘要
目的:子宫内膜癌(EC)是妇女最常见的癌症类型之一。虽然苏木精-伊红(H&E)染色仍是组织学分析的标准,但免疫组化(IHC)方法可提供分子水平的可视化。我们的研究提出了一种数字染色方法,通过 H&E 染色法生成 EC 肿瘤整张玻片图像中 Ki-67 的苏木精-3,3'-二氨基联苯胺(H-DAB)IHC 染色法:我们采用了一种颜色不混合技术,从染色剂的光密度(OD)得出染色剂密度图,并利用 U-Net 进行端到端推理。我们利用数字染色和物理染色的标记指数(LI)之间的皮尔逊相关性评估了所提方法的有效性。我们的研究设计了两种不同的交叉验证方案:滑动内验证和交叉案例验证(CCV)。在广泛使用的切片内验证方案中,训练集和验证集可能包括来自同一张切片的不同区域。严格的 CCV 验证方案严格禁止任何验证切片参与训练:结果:所提出的方法得到了保留组织学特征的高分辨率数字染色,表明在 Ki-67 LI 方面与物理染色具有可靠的相关性。在滑动内方案中,使用滑动内补丁的偏倚准确度(如 R = 0.98)明显高于 CCV。CCV 方案保留了数字染色与物理 IHC 计算的 LI 之间的相关性(如 R = 0.66)。从 H&E 染色结果推断 IHC 染色结果的 OD 增强了相关性指标,优于使用 RGB 空间的基线模型:我们的研究表明,利用深度学习可以从 H&E 图像中获得分子级的见解。此外,OD 推理带来的改进表明,通过每染色分析为数字染色创建更具通用性的模型是一种可行的方法。
Transformation from hematoxylin-and-eosin staining to Ki-67 immunohistochemistry digital staining images using deep learning: experimental validation on the labeling index.
Purpose: Endometrial cancer (EC) is one of the most common types of cancer affecting women. While the hematoxylin-and-eosin (H&E) staining remains the standard for histological analysis, the immunohistochemistry (IHC) method provides molecular-level visualizations. Our study proposes a digital staining method to generate the hematoxylin-3,3'-diaminobenzidine (H-DAB) IHC stain of Ki-67 for the whole slide image of the EC tumor from its H&E stain counterpart.
Approach: We employed a color unmixing technique to yield stain density maps from the optical density (OD) of the stains and utilized the U-Net for end-to-end inference. The effectiveness of the proposed method was evaluated using the Pearson correlation between the digital and physical stain's labeling index (LI), a key metric indicating tumor proliferation. Two different cross-validation schemes were designed in our study: intraslide validation and cross-case validation (CCV). In the widely used intraslide scheme, the training and validation sets might include different regions from the same slide. The rigorous CCV validation scheme strictly prohibited any validation slide from contributing to training.
Results: The proposed method yielded a high-resolution digital stain with preserved histological features, indicating a reliable correlation with the physical stain in terms of the Ki-67 LI. In the intraslide scheme, using intraslide patches resulted in a biased accuracy (e.g., ) significantly higher than that of CCV. The CCV scheme retained a fair correlation (e.g., ) between the LIs calculated from the digital stain and its physical IHC counterpart. Inferring the OD of the IHC stain from that of the H&E stain enhanced the correlation metric, outperforming that of the baseline model using the RGB space.
Conclusions: Our study revealed that molecule-level insights could be obtained from H&E images using deep learning. Furthermore, the improvement brought via OD inference indicated a possible method for creating more generalizable models for digital staining via per-stain analysis.
期刊介绍:
JMI covers fundamental and translational research, as well as applications, focused on medical imaging, which continue to yield physical and biomedical advancements in the early detection, diagnostics, and therapy of disease as well as in the understanding of normal. The scope of JMI includes: Imaging physics, Tomographic reconstruction algorithms (such as those in CT and MRI), Image processing and deep learning, Computer-aided diagnosis and quantitative image analysis, Visualization and modeling, Picture archiving and communications systems (PACS), Image perception and observer performance, Technology assessment, Ultrasonic imaging, Image-guided procedures, Digital pathology, Biomedical applications of biomedical imaging. JMI allows for the peer-reviewed communication and archiving of scientific developments, translational and clinical applications, reviews, and recommendations for the field.