Clinical Application Value of Deep Learning-Based "Opportunistic Screening" for Malignant Tumors on Routine Non-Contrast Chest-Abdomen-Pelvis CT

ConditionTumor
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorLian Yang

About this trial

This study aims to develop and validate a deep learning-based opportunistic multi-cancer screening system using routine non-contrast chest-abdomen-pelvis CT examinations, including CHANCE-Breast, CHANCE-Liver, CHANCE-Kidney, and CHANCE-Bladder, for the early detection of breast, liver, kidney, and bladder cancers. In addition, the study will assess a human-AI collaborative framework to determine its potential for improving cancer detection and reducing missed diagnoses in clinical practice.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients with a confirmed diagnosis of the target malignancy who received treatment at our institution;

Diagnostic-quality CT images without substantial metal or motion artifacts and with complete anatomical coverage of the target organ (breast, liver, kidney, or bladder);

Availability of complete pre-treatment non-contrast CT imaging data.

Disqualifiers

Non-diagnostic image quality;

Absence of a definitive reference-standard diagnosis;

Incomplete clinical or imaging data.

Trial population

Patients with a confirmed diagnosis of the target malignancy who received treatment.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

100,000 Participants
are grouped into 3 trial groups
Group A: Positive Group / Malignant Cohort
Group B: Negative Control Group I / Benign Cohort
Group C: Negative Control Group II / Healthy Cohort

Trial outcomes

Primary outcomes

1

Accuracy

Proportion of correct classifications

Time frame
1.5 years
2

Sensitivity

Proportion of true positive cases

Time frame
1.5years
3

Specificity

Proportion of true negative cases

Time frame
1.5years

Secondary outcomes

1

Delta Sensitivity (AI-assisted vs. unassisted)

Absolute difference in sensitivity between AI-assisted and unassisted human readings

Time frame
1.5years
2

Delta Specificity (AI-assisted vs. unassisted)

Absolute difference in specificity between AI-assisted and unassisted human readings

Time frame
1.5years
3

Delta Accuracy (AI-assisted vs. unassisted)

Absolute difference in accuracy between AI-assisted and unassisted human readings

Time frame
1.5years

Other outcomes

Sponsors and contacts

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Lian Yang

Lead sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: