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NCT06703944Enrolling by invitation

Risk Model for Metastasis Detection of Neuroblastoma

Bone Marrow Cytology-based Artificial Intelligence Model for Detection and Prognosis of Neuroblastoma

Source: ClinicalTrials.gov · Last updated 15 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
500 (estimated)
First submitted
19 Nov 2024
Start date
1 Dec 2024
Primary completion date
1 Jul 2025
Lead sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
NCT number
NCT06703944

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 1 Dec 2024 to the primary completion date, 1 Jul 2025
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • The participant with concurrent diagnosis of other malignancies.
  • The participant with NB who has previously received chemotherapy and/or radiotherapy.

Other

  • The participant with incomplete clinical data, the metastasis state of bone marrow and/or bone is unclear.
  • The participant was excluded due to non-representative specimens, such as unclear or faded Wright-Giemsa staining of bone marrow smear.

Who the study is looking for

  • 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.
  • The participant diagnosed with NB at other hospitals who have not received chemotherapy or radiotherapy.
  • 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.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Children's Hospital, Zhejiang University School of Medicine
Coordinator of this site? Confirm its status
HangzhouChinaUnknown status
Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
Shenzhen Children's Hospital
Coordinator of this site? Confirm its status
ShenzhenChinaUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.