High-efficiency spatially guided learning network for lymphoblastic leukemia detection in bone marrow microscopy images.

Journal: Computers in biology and medicine
Published Date:

Abstract

Leukemia is a hematologic tumor that proliferates in bone marrow and seriously affects the survival of patients. Early and accurate diagnosis is crucial for effective leukemia treatment. Traditional diagnostic methods rely on experts' subjective analysis of bone marrow smears microscopic images. This approach is time-consuming and complex. Despite recent advances in deep learning, automated leukemia detection remains limited due to the scarcity of high-quality datasets, the prevailing focus on single-cell image classification rather than precise cell-level detection in whole slide images, along with challenges such as morphological heterogeneity, uneven staining, scale variation, and occluded cell boundary in bone marrow smears. To address these challenges, we construct a novel dataset comprising 1794 high-quality microscopic images, establishing a new benchmark for lymphocytic leukemia detection. Additionally, we develop a fully automated diagnostic method based on spatially-guided learning (SGLNet), enabling rapid whole slide analysis of leukemia. Specifically, we introduce several innovative enhancements to the baseline algorithm, including the spatially-guided learning framework, scale-aware fusion module, small object-enhancing mechanisms, and efficient intersection over union loss function. These improvements effectively address the impact of morphological similarity and complex backgrounds in leukemia detection, significantly enhancing detection accuracy. Finally, the results show that SGLNet achieves mean average precision scores of 95.9 % and 98.6 % in detecting acute lymphoblastic leukemia and chronic lymphocytic leukemia, respectively. These results demonstrate the efficiency and accuracy of our method in identifying lymphoblastic leukemia cells, significantly enhancing large-scale clinical diagnosis, and supporting clinicians in developing personalized treatment plans.

Authors

  • Liye Mei
    The Institute of Technological Sciences, Wuhan University, Wuhan, China.
  • Chentao Lian
    School of Computer Science, Hubei University of Technology, Wuhan, 430068, China.
  • Suyang Han
    The Second Clinical School of Wuhan University, Zhongnan Hospital of Wuhan University, 430071, Wuhan, China.
  • Zhaoyi Ye
    The Institute of Technological Sciences, Wuhan University, Wuhan, China.
  • Yuyang Hua
    School of Computer Science, Hubei University of Technology, Wuhan, 430068, China.
  • Meixing Sun
    School of Computer Science, Hubei University of Technology, Wuhan, 430068, China.
  • Jing He
    School of Management, Guilin University of Aerospace Technology, Guilin, China.
  • Zhiwei Ye
    School of Computer Science, Hubei University of Technology, Wuhan 430068, China.
  • Mengqing Mei
    School of Computer Science, Hubei University of Technology, Wuhan, 430068, China; Hubei Key Laboratory of Green Intelligent Computing Power Network, Hubei University of Technology, Wuhan, 430068, China.
  • Yaxiaer Yalikun
    Division of Materials Science, Nara Institute of Science and Technology, 8916-5 Takayamacho, Ikoma, Nara, 630-0192, Japan; Center for Biosystems Dynamics Research (BDR), RIKEN, 1-3 Yamadaoka, Suita, Osaka, 565-0871, Japan. Electronic address: yaxiaer@ms.naist.jp.
  • Hui Shen
    College of Mechatronics and Automation, National University of Defense Technology, Changsha, China.
  • Cheng Lei
  • Bei Xiong
    The Department of Hematology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China. Electronic address: zn001587@whu.edu.cn.

Keywords

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