Clinical trial · Observational
Risk Model for Metastasis Detection of Neuroblastoma
Bone Marrow Cytology-based Artificial Intelligence Model for Detection and Prognosis of Neuroblastoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Neuroblastoma (NB) is the most common extracranial solid tumor in children, accounting for about 15% of tumor-related mortality. NB patients in high-risk group are prone to bone marrow and/or bone metastases with low five-year overall survival rate. The artificial intelligence (AI) and deep learning technologies have potential to identifying morphological characteristics of bone marrow cytology in clinical practice. In this study, the investigators construct and evaluate the bone marrow cytology-based AI model for detection and prognosis of NB. The main questions of the study as follows: The question 1: Dose bone marrow cytology-based AI model work for prediction of bone marrow metastasis in NB? The question 2: Dose bone marrow cytology-based AI model work for prediction of bone metastasis in NB? The question 3: Dose bone marrow cytology-based AI model have potential to assist doctors in making individualized predictions of survival outcome? The investigators will retrospectively obtain the participants with NB between January 2019 and June 2024. The follow-up date ended on June 30, 2024. The internal cohort including participants from Xinhua Hospital, Shanghai Jiao Tong University School of Medicine. The independent external cohorts including participants form Children's Hospital, Zhejiang University School of Medicine and Shenzhen Children's Hospital. The investigators collect the clinical data of enrolled participants at the time of the patients' initial admission to the hospital, prior to receiving treatment. The clinical information including age, gender, primary tumor location, tumor grade, bone marrow metastasis state, bone metastasis state, genetic aberrations (MYCN amplification, Chromosome 1p deletion, Chromosome 11q deletion) and lab variables (peripheral blood cell count, bone marrow cytology indicators, the serum concentration of lactate dehydrogenase, neuron specific enolase). This study is a non-interventional observational study, there is no risk to the participants and investigators. Participants get these benefits: 1. Early Detection: The model helps in early risk identification and personalize treatment. 2. Convenience: Because the model relies on general lab tests, it is easy to carry out can reduce invasive diagnostic procedures. 3. Cost-Effective: Using existing clinical data from routine tests can make the prediction process more cost-effective. 4. Data-Driven Decisions: The AI model improve diagnostic efficiency and support the medical decision.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Bone Marrow Metastasis | — | UNRESOLVED | — |
| Bone Metastases | — | UNRESOLVED | — |
| Neuroblastoma (NB) | Neuroblastoma | ONTOLOGY_EXACT | 0.85 |
| Prognosis | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| risk model in diagnosis and prognosis | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Neuroblastoma With Bone Marrow Metastasis Group
- description
- For the diagnosis of neuroblastoma with bone marrow metastasis, the medical practices including as follows: bone marrow biopsy, bone marrow cytology of aspiration smear, flow cytometry and positron emission tomography-computed tomography(PET-CT). Bone marrow biopsy or smear analysis may reveal characteristic NB cells. Flow cytometry may detect NB cells with phenotype of cluster of differentiation antigen 45(CD45)-/cluster of differentiation antigen 56(CD56)+/cluster of differentiation antigen 81(CD81)+/GD2 ganglioside (GD2)+. PET/CT imaging reveal the metastatic NB cells in term of metabolic activity and spatial distribution of metastatic involvement. A positive result from any of these methods is sufficient for diagnosed as NB with bone marrow metastasis.
- interventionNames
- Other: risk model in diagnosis and prognosis
- label
- Neuroblastoma Without Bone Marrow Metastasis Group
- description
- For the diagnosis of bone marrow metastasis in the enrolled participants, if there is no positive result from any of these tests as follows: bone marrow biopsy, bone marrow cytology of smear, flow cytometry or PET/CT, the participant is classified into the Neuroblastoma Without Bone Marrow Metastasis Group.
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: 1. The participant newly diagnosed with NB according to the International Neuroblastoma Risk Group Staging System (INRGSS). The diagnosis completed by experienced pathologist and correlated with clinical and/or radiological findings. 2. The participant diagnosed with NB at other hospitals who have not received chemotherapy or radiotherapy. 3. The participant with NB has performed bone marrow smear analysis as routine examination. The bone marrow smear stained with Wright-Giemsa was made according to standard protocols. Exclusion Criteria: 1. The participant with concurrent diagnosis of other malignancies. 2. The participant with NB who has previously received chemotherapy and/or radiotherapy. 3. The participant with incomplete clinical data, the metastasis state of bone marrow and/or bone is unclear. 4. The participant was excluded due to non-representative specimens, such as unclear or faded Wright-Giemsa staining of bone marrow smear.
References
Publications (1)
- DERIVEDMa J, Yao Q, Fu X, Xia Z, Yue Y, Xu D, Yuan X, Zhao L, Wang J, Dong A, Gao L, Yang J, Shen L, Zheng Y, Ni S. Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology. J Transl Med. 2026 Apr 7;24(1):691. doi: 10.1186/s12967-026-08069-2. PMID 41947227