NCT06853457

Brief Summary

To develop and validate a CT-based transfer learning radiomics model for predicting response to initial TAE in GEP-NETLM patients and compare its performance with traditional radiomics and clinical models.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
257

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2014

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2014

Completed
8.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2022

Completed
1.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

February 23, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

March 3, 2025

Completed
Last Updated

March 3, 2025

Status Verified

February 1, 2025

Enrollment Period

8.8 years

First QC Date

February 23, 2025

Last Update Submit

February 28, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • The efficacy of TAE

    Complete multiphase contrast-enhanced CT images were collected preoperatively and postoperatively. The efficacy of TAE was assessed based on RECIST 1.1 criteria. Patients were classified as objective responders (those achieving complete response \[CR\] or partial response \[PR\]) or non-responders (those with stable disease \[SD\] or progressive disease \[PD\]) through evaluation of target lesions.

    Within one month prior and 4-6 weeks following the initial TAE.

Study Arms (2)

training set

The training set consisted of patients from January 2014 to December 2020.

testing set

the testing set included patients from January 2021 to September 2022.

Eligibility Criteria

Age18 Years - 78 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

This study retrospectively included gastroenteropancreatic neuroendocrine tumors liver metastasis patients who receive initial transarterial embolization from January 2014 to September 2022 at The First Affiliated Hospital of Sun Yat-sen University.

You may qualify if:

  • (a) Clinical diagnosed as gastroenteropancreatic neuroendocrine tumor liver metastases; (b) Received initial transarterial embolization therapy; (c) Underwent multi-phase ceCT scans pre-TAE (≤1 month) and post-TAE (4-6 weeks).

You may not qualify if:

  • (a) Neuroendocrine carcinoma (NEC) or other malignancies. (b) Received other liver metastasis treatments. (c) Lack of Multi-phase ceCT scans records. (d) CT images with artifacts or no visible lesions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neuroendocrine Tumors

Condition Hierarchy (Ancestors)

Neuroectodermal TumorsNeoplasms, Germ Cell and EmbryonalNeoplasms by Histologic TypeNeoplasmsNeoplasms, Nerve Tissue

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

February 23, 2025

First Posted

March 3, 2025

Study Start

January 1, 2014

Primary Completion

September 30, 2022

Study Completion

September 1, 2024

Last Updated

March 3, 2025

Record last verified: 2025-02