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Transformation from hematoxylin-and-eosin staining to Ki-67 immunohistochemistry digital staining images using deep learning: experimental validation on the labeling index.
Ji, Cunyuan; Oshima, Kengo; Urata, Takumi; Kimura, Fumikazu; Ishii, Keiko; Uehara, Takeshi; Suzuki, Kenji; Takeyama, Saori; Yamaguchi, Masahiro.
Afiliación
  • Ji C; Tokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.
  • Oshima K; Shinshu University, School of Health Sciences, Department of Biomedical Laboratory Sciences, Matsumoto, Japan.
  • Urata T; Tokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.
  • Kimura F; Shinshu University, School of Health Sciences, Department of Biomedical Laboratory Sciences, Matsumoto, Japan.
  • Ishii K; Okaya City Hospital, Division of Diagnostic Pathology, Okaya, Japan.
  • Uehara T; Shinshu University, School of Medicine, Department of Laboratory Medicine, Matsumoto, Japan.
  • Suzuki K; Tokyo Institute of Technology, Institute of Innovative Research, Biomedical AI Research Unit, Yokohama, Japan.
  • Takeyama S; Tokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.
  • Yamaguchi M; Tokyo Institute of Technology, School of Engineering, Department of Information and Communications Engineering, Yokohama, Japan.
J Med Imaging (Bellingham) ; 11(4): 047501, 2024 Jul.
Article en En | MEDLINE | ID: mdl-39087085
ABSTRACT

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., R = 0.98 ) significantly higher than that of CCV. The CCV scheme retained a fair correlation (e.g., R = 0.66 ) 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.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Med Imaging (Bellingham) Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Med Imaging (Bellingham) Año: 2024 Tipo del documento: Article País de afiliación: Japón