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Predicting Tumor Origin Based on Deep Learning of Lymph Node Puncture Cytology

A Multicenter Study on Predicting Tumor Origin Based on Deep Learning of Lymph Node Puncture Cytology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06810349
Enrollment
10000
Registered
2025-02-05
Start date
2024-11-11
Completion date
2025-12-31
Last updated
2025-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lymph Nodes With Tumor Metastasis

Keywords

Primary unknown tumor origin, Deep learning, Cytopathology

Brief summary

In this study, the investigators aimed to construct a deep learning diagnostic model that uses cytological images to predict primary unknown tumor origins in patients with tumors combined with lymph node metastases. After the model is constructed, the model will be validated by a large-scale test set to test the model performance. The investigators also propose to compare the performance of the constructed model in diagnosing cytology smears compared to human pathologists.

Interventions

None listed

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* From West China Hospital of Sichuan University (October 1, 2008-August 31, 2024) with corresponding clinical data, including age, sex, specimen puncture site, pathologic diagnosis, pathologic type, whether immunocytochemistry was added, clinical diagnosis, lesion site, co-morbidities, history of malignancy, treatment modality, occurrence of postoperative complications, total number of days of hospitalization postoperatively, and survival time; * From the Department of Pathology of the First Affiliated Hospital of Zhengzhou University, the Sichuan Provincial Cancer Hospital, and the Cancer Hospital of the Chinese Academy of Medical Sciences (January 1, 2020-August 31, 2024) with corresponding clinical data, including age, sex, specimen puncture site, pathologic diagnosis, pathologic type, whether immunocytochemistry was added, clinical diagnosis, lesion site, co-morbidities, history of malignancy, treatment modality, occurrence of postoperative complications, total number of days of hospitalization postoperatively, and survival time.

Exclusion criteria

* Images lacking any supporting clinical or pathologic evidence to support a primary origin and its corresponding clinical information; * Blank, poorly focused, and low-quality images containing severe artifacts and their corresponding clinical information.

Design outcomes

Primary

MeasureTime frameDescription
Model performance metrics1 yearModel performance was evaluated by Positive Predictive Value (PPV), Negative Predictive Value (NPV), Accuracy, Sensitivity and Specificity.

Countries

China

Contacts

Primary ContactJianyong Lei
guosiyin2000@163.com02885423822

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026