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Deep Learning Signature for Predicting the Novel Grading System of Clinical Stage I Lung Adenocarcinoma

Deep Learning Signature Based on PET-CT Images for Predicting the Novel Grading System of Clinical Stage I Lung Adenocarcinoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05736991
Enrollment
600
Registered
2023-02-21
Start date
2022-11-01
Completion date
2023-04-30
Last updated
2023-02-21

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

Conditions

Grading System, Lung Adenocarcinoma, Radiomics

Brief summary

The purpose of this study is to evaluate the performance of a PET/ CT-based deep learning signature for predicting the grade 3 tumors based on the novel grading system in clinical stage stage I lung adenocarcinoma based on a multicenter prospective cohort.

Interventions

DIAGNOSTIC_TESTPET/CT-based Radiomics Signature

Radiomics Signature Based on PET-CT for Predicting the Novel Grading System of Clinical Stage I Lung Adenocarcinoma

Sponsors

Ningbo No.2 Hospital
CollaboratorOTHER
Zunyi Medical College
CollaboratorOTHER
The First Affiliated Hospital of Nanchang University
CollaboratorOTHER
Shanghai Pulmonary Hospital, Shanghai, China
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

(1) Participants scheduled for surgery for radiological finding of pulmonary lesions from the preoperative thin-section CT scans; (2) The maximum diameter of lesion less than 4 cm on CT scans; (3) The maximum short axis diameter of lymph nodes less than 1 cm on CT scan; (4) The SUVmax of hilar and mediastinal lymph nodes less than 2.5; (5) Pathological confirmation of primary lung adenocarcinoma; (5) Age ranging from 20-75 years; (6) Obtained written informed consent.

Exclusion criteria

(1) Multiple lung lesions; (2) Poor quality of PET-CT images; (3) Participants with incomplete clinical information; (4) Mucinous adenocarcinomas; (5) Participants who have received neoadjuvant therapy.

Design outcomes

Primary

MeasureTime frameDescription
Area under the receiver operating characteristic curve2022.11-2023.4Area under the receiver operating characteristic curve

Secondary

MeasureTime frameDescription
Sensitivity2022.11-2023.4Sensitivity
Specificity2022.11-2023.4Specificity
Positive predictive value2022.11-2023.4Positive predictive value
Negative predictive value2022.11-2023.4Negative predictive value
Accuracy2022.11-2023.4Accuracy

Countries

China

Outcome results

None listed

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