Potential rapid intraoperative cancer diagnosis using dynamic full-field optical coherence tomography and deep learning: A prospective cohort study in breast cancer patients

被引:3
|
作者
Zhang, Shuwei [1 ]
Yang, Bin [2 ,3 ]
Yang, Houpu [1 ]
Zhao, Jin [1 ]
Zhang, Yuanyuan [4 ]
Gao, Yuanxu [5 ]
Monteiro, Olivia [5 ]
Zhang, Kang [5 ,6 ]
Liu, Bo [7 ]
Wang, Shu [1 ]
机构
[1] Peking Univ Peoples Hosp, Breast Ctr, Beijing 100044, Peoples R China
[2] Capital Univ Econ & Business, China ESG Inst, Beijing 100070, Peoples R China
[3] Beijing Univ Technol, Fac Informat Technol, Beijing 100124, Peoples R China
[4] Peking Univ, Peoples Hosp, Dept Pathol, Beijing 100044, Peoples R China
[5] Macau Univ Sci & Technol, Fac Med, Ctr Biomed & Innovat, Macau 999078, Peoples R China
[6] Peking Univ, Coll Future Technol, Beijing 100091, Peoples R China
[7] Massey Univ, Sch Math & Computat Sci, Auckland 0745, New Zealand
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Cancer diagnosis; Breast neoplasms; Dynamic full -field optical coherence; tomography; Deep learning; Image classification; MARGIN ASSESSMENT; TISSUE;
D O I
10.1016/j.scib.2024.03.061
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
An intraoperative diagnosis is critical for precise cancer surgery. However, traditional intraoperative assessments based on hematoxylin and eosin (H&E) histology, such as frozen section, are time-, resource-, and labor-intensive, and involve specimen-consuming concerns. Here, we report a near-realtime automated cancer diagnosis workflow for breast cancer that combines dynamic full -field optical coherence tomography (D-FFOCT), a label -free optical imaging method, and deep learning for bedside tumor diagnosis during surgery. To classify the benign and malignant breast tissues, we conducted a prospective cohort trial. In the modeling group ( n = 182), D-FFOCT images were captured from April 26 to June 20, 2018, encompassing 48 benign lesions, 114 invasive ductal carcinoma (IDC), 10 invasive lobular carcinoma, 4 ductal carcinoma in situ (DCIS), and 6 rare tumors. Deep learning model was built up and fine-tuned in 10,357 D-FFOCT patches. Subsequently, from June 22 to August 17, 2018, independent tests ( n = 42) were conducted on 10 benign lesions, 29 IDC, 1 DCIS, and 2 rare tumors. The model yielded excellent performance, with an accuracy of 97.62%, sensitivity of 96.88% and specificity of 100%; only one IDC was misclassified. Meanwhile, the acquisition of the D-FFOCT images was nondestructive and did not require any tissue preparation or staining procedures. In the simulated intraoperative margin evaluation procedure, the time required for our novel workflow (approximately 3 min) was significantly shorter than that required for traditional procedures (approximately 30 min). These findings indicate that the combination of D-FFOCT and deep learning algorithms can streamline intraoperative cancer diagnosis independently of traditional pathology laboratory procedures. (c) 2024 Science China Press. Published by Elsevier B.V. and Science China Press.
引用
收藏
页码:1748 / 1756
页数:9
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