Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology

Bone marrow (BM) is the most common site of metastatic disease at diagnosis and a frequent site of relapse in neuroblastoma. Digital cytology images of BM smears offer a rich data source for artificial intelligence models, which may potentially facilitate more cost-effective risk stratification within the diagnostic workflow. This study aims to develop an interpretable cytology model for detecting BM metastasis in pediatric neuroblastoma. This retrospective diagnostic study used Wright-Giemsa–stained BM cytology images from 359 neuroblastoma patients who underwent BM screening between January 2019 and June 2024 across multiple centers in China. After the quality evaluation, we generated 1384,007 patches from BM digital cytology to develop and validate the cytology model. In the model construction, we integrated a multiple-instance learning framework with convolutional neural networks to extract cytology features, referred to as cMIL. The cytology model was trained for BM metastasis detection and risk stratification with interpretability. For metastasis detection, the cytology model achieved an AUC of 0.924 (95% CI, 0.775–1.000) in the training cohort. Performance remained strong in external validation, with AUCs of 0.826 (95% CI, 0.741–0.911) in Cohort A and 0.795 (95% CI, 0.684–0.906) in Cohort B, indicating consistent performance across independent multicenter cohorts. The cMIL score also successfully stratified patients in terms of survival outcomes (log-rank p < 0.05). Interpretability analyses further demonstrated that the model’s predictions were associated with clinically relevant cytological features. In this retrospective diagnostic study, the developed cytology model demonstrated high discriminative performance in detecting BM metastasis and captured the underlying complexity and heterogeneity of BM. These findings suggest that the cytology model could serve as a promising tool for improving metastasis detection and risk stratification in patients with neuroblastoma, potentially contributing to personalized treatment strategies and enhanced disease monitoring. This retrospective study was registered with ClinicalTrials.gov (NCT06703944) on November 21, 2024. Study title: bone marrow cytology-based artificial intelligence model for detection and prognosis of neuroblastoma. (https://register.clinicaltrials.gov).

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Publication Details

Journal
Journal of Translational Medicine
Published
2026-04-07
DOI
https://doi.org/10.1186/s12967-026-08069-2
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology

Jun Yang, Dongqing Xu, Yaoting Yue, Xiaoying Fu et al.
Journal of Translational Medicine
Neuroblastoma Research and Treatments
article

Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology

Jun Yang, Dongqing Xu, Yaoting Yue, Xiaoying Fu, Liebin Zhao, Juan Ma, Limei Gao, Yingxia Zheng, Yi-Xiang Wang, Shaoqing Ni, Zhouqi Xia, Qiang Yao, Xiaojun Yuan, Ao Dong
article en

Abstract

Bone marrow (BM) is the most common site of metastatic disease at diagnosis and a frequent site of relapse in neuroblastoma. Digital cytology images of BM smears offer a rich data source for artificial intelligence models, which may potentially facilitate more cost-effective risk stratification within the diagnostic workflow. This study aims to develop an interpretable cytology model for detecting BM metastasis in pediatric neuroblastoma. This retrospective diagnostic study used Wright-Giemsa–stained BM cytology images from 359 neuroblastoma patients who underwent BM screening between January 2019 and June 2024 across multiple centers in China. After the quality evaluation, we generated 1384,007 patches from BM digital cytology to develop and validate the cytology model. In the model construction, we integrated a multiple-instance learning framework with convolutional neural networks to extract cytology features, referred to as cMIL. The cytology model was trained for BM metastasis detection and risk stratification with interpretability. For metastasis detection, the cytology model achieved an AUC of 0.924 (95% CI, 0.775–1.000) in the training cohort. Performance remained strong in external validation, with AUCs of 0.826 (95% CI, 0.741–0.911) in Cohort A and 0.795 (95% CI, 0.684–0.906) in Cohort B, indicating consistent performance across independent multicenter cohorts. The cMIL score also successfully stratified patients in terms of survival outcomes (log-rank p < 0.05). Interpretability analyses further demonstrated that the model’s predictions were associated with clinically relevant cytological features. In this retrospective diagnostic study, the developed cytology model demonstrated high discriminative performance in detecting BM metastasis and captured the underlying complexity and heterogeneity of BM. These findings suggest that the cytology model could serve as a promising tool for improving metastasis detection and risk stratification in patients with neuroblastoma, potentially contributing to personalized treatment strategies and enhanced disease monitoring. This retrospective study was registered with ClinicalTrials.gov (NCT06703944) on November 21, 2024. Study title: bone marrow cytology-based artificial intelligence model for detection and prognosis of neuroblastoma. (https://register.clinicaltrials.gov).

Journal of Translational Medicine
Shanghai University (CN), Shanghai Jiao Tong University (CN), XinHua Hospital (CN), Beijing Academy of Artificial Intelligence (CN), Children's Hospital of Zhejiang University (CN), Zhejiang Pharmaceutical College (CN), Shenzhen Children's Hospital (CN), Zhejiang University (CN)
National Natural Science Foundation of China, Key Technologies Research and Development Program, Science and Technology Innovation Plan Of Shanghai Science and Technology Commission
Reduced inequalities
Openalex Percentile: Top 24%
Neuroblastoma Research and Treatments
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