A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals.
A deep learning diagnostic platform for diffuse large B-cell lymphoma with high accuracy across multiple hospitals.
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跨多家医院的弥漫性大b细胞淋巴瘤高精度深度学习诊断平台。
DOI:
10.1038/s41467-020-19817-3
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发表时间:
2020-11-26
影响因子:
16.6
通讯作者:
Li S
中科院分区:
文献类型:
--
作者:
Li D;Bledsoe JR;Zeng Y;Liu W;Hu Y;Bi K;Liang A;Li S
Diagnostic histopathology is a gold standard for diagnosing hematopoietic malignancies. Pathologic diagnosis requires labor-intensive reading of a large number of tissue slides with high diagnostic accuracy equal or close to 100 percent to guide treatment options, but this requirement is difficult to meet. Although artificial intelligence (AI) helps to reduce the labor of reading pathologic slides, diagnostic accuracy has not reached a clinically usable level. Establishment of an AI model often demands big datasets and an ability to handle large variations in sample preparation and image collection. Here, we establish a highly accurate deep learning platform, consisting of multiple convolutional neural networks, to classify pathologic images by using smaller datasets. We analyze human diffuse large B-cell lymphoma (DLBCL) and non-DLBCL pathologic images from three hospitals separately using AI models, and obtain a diagnostic rate of close to 100 percent (100% for hospital A, 99.71% for hospital B and 100% for hospital C). The technical variability introduced by slide preparation and image collection reduces AI model performance in cross-hospital tests, but the 100% diagnostic accuracy is maintained after its elimination. It is now clinically practical to utilize deep learning models for diagnosis of DLBCL and ultimately other human hematopoietic malignancies. Replacing diagnostic histopathology with AI-based tools requires large training datasets and robustness to sample variability. Here, the authors present a deep learning platform with high accuracy in large diffuse B-cell lymphoma diagnosis across multiple hospitals, trained on small datasets.
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影响因子:
11.1
作者:
Khosravi P;Kazemi E;Imielinski M;Elemento O;Hajirasouliha I
通讯作者:
Hajirasouliha I
影响因子:
64.8
作者:
Esteva A;Kuprel B;Novoa RA;Ko J;Swetter SM;Blau HM;Thrun S
通讯作者:
Thrun S
影响因子:
82.9
作者:
Titano, Joseph J.;Badgeley, Marcus;Oermann, Eric K.
通讯作者:
Oermann, Eric K.
影响因子:
64.8
作者:
Mnih, Volodymyr;Kavukcuoglu, Koray;Hassabis, Demis
通讯作者:
Hassabis, Demis
影响因子:
64.8
作者:
McKinney, Scott Mayer;Sieniek, Marcin;Shetty, Shravya
通讯作者:
Shetty, Shravya