RET-US Study - Ultrasound-Based Prediction of RET Alterations and Lateral-Neck Metastasis in Thyroid Cancer

NCT ID: NCT07042984

Last Updated: 2025-06-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

800 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-07-01

Study Completion Date

2029-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Why is this study being done? RET gene alterations occur in only 5-10 % of papillary thyroid cancers, but they can change how surgeons treat the disease. Gene testing is costly and not always performed, so many RET-positive tumours are missed. Researchers have built a computer program (artificial-intelligence or "AI" model) that reads routine thyroid ultrasound images and predicts whether the tumour carries a RET alteration and whether the cancer has already spread to lymph-nodes in the side of the neck.

What will happen in this study?

About 800 adults who are scheduled for thyroid-cancer surgery will take part. Each participant will:

* have a standard pre-operative ultrasound exam (no extra scanning time),
* give a routine fine-needle sample for a 14-gene panel test (results in 24 h), and
* allow the AI model to analyse the ultrasound images in the background. Doctors making treatment decisions will not see the AI result. After surgery, the research team will compare the AI predictions with the gene-panel result and the final pathology report.

Main goal: To find out how accurately the AI model detects RET alterations. Secondary goals: To measure the model's ability to predict lymph-node spread, and to compare costs between ultrasound-only prediction and full gene testing.

Benefits and risks: Participants will receive the current standard of care; there is no added risk beyond the usual ultrasound and needle biopsy. The study could lead to faster, less expensive ways to identify high-risk thyroid cancers in the future.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Background RET rearrangements or point mutations drive a minority of papillary thyroid carcinomas (PTC) yet are associated with aggressive behaviour and may qualify patients for selective RET inhibitors. Because of low prevalence, RET testing is often omitted, resulting in under-recognition. Recent work shows that high-resolution ultrasound contains radiomic signatures linked to tumour genotypes. A deep-learning model (EfficientNet-B3 backbone with dual segmentation + multi-label heads) was trained on 1 000 retrospectively collected cases, including 74 RET-positive tumours augmented with GAN-based synthetic images, achieving an AUC of 0.87 for RET prediction in internal cross-validation.

Objectives Primary: validate the AI model's area under the receiver-operating characteristic curve (AUC) for RET alteration detection in a prospective cohort.

Secondary: (i) sensitivity/specificity for RET; (ii) accuracy for predicting lateral-neck (pN1b) metastasis; (iii) incremental cost per correct RET diagnosis; (iv) concordance between AI probability score and lymph-node burden.

Design Single-arm, prospective observational cohort (n = 800). Consecutive eligible patients will undergo: (1) routine pre-operative thyroid ultrasound; (2) upload of DICOM files to a cloud inference server; (3) rapid 14-gene next-generation sequencing panel on FNA or paraffin tissue (includes RET fusions KIF5B, CCDC6, NCOA4 and point mutations M918T, V804). Surgeons remain blinded to AI output. Surgical specimens provide ground truth for pN staging. Data captured in REDCap; statistical analysis uses DeLong test for AUC and McNemar test for paired accuracy.

Eligibility Adults 18-75 y with radiologically suspected PTC, planned thyroidectomy, and consent for gene testing. Exclusions: re-operative neck, medullary/anaplastic carcinoma, pregnancy, eGFR \< 30 mL min-¹ 1.73 m-².

Sample Size With expected RET prevalence 6 % and target AUC ≥ 0.80 vs null 0.50, 800 cases provide 90 % power (α = 0.05).

Ethics \& Oversight IRB approved; minimal-risk diagnostic study. Ultrasound and FNA are standard-of-care; AI inference uses de-identified images. Results will be disseminated via peer-reviewed journals and conference presentations.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Papillary Thyroid Carcinoma Thyroid Neoplasms RET Proto-Oncogene Mutation Lymphatic Metastasis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Prospective Thyroid Cancer Cohort

Consecutive adults (18-75 y) with ultrasound-suspected papillary thyroid carcinoma scheduled for surgery. Each participant undergoes standard pre-operative ultrasound, rapid 14-gene next-generation sequencing (NGS) panel, and blinded AI analysis of the ultrasound images. No treatment allocation is made; data are collected prospectively to validate the AI model's ability to detect RET alterations and predict lateral-neck lymph-node metastasis.

AI-Ultrasound RET Prediction

Intervention Type DIAGNOSTIC_TEST

Deep-learning algorithm that analyses thyroid ultrasound DICOM images and outputs a probability score for RET gene alteration and lateral-neck lymph-node metastasis; run offline, results blinded to treating surgeons.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

AI-Ultrasound RET Prediction

Deep-learning algorithm that analyses thyroid ultrasound DICOM images and outputs a probability score for RET gene alteration and lateral-neck lymph-node metastasis; run offline, results blinded to treating surgeons.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age 18-75 years, able to provide written informed consent.
* Pre-operative ultrasound findings highly suggestive of papillary thyroid carcinoma.
* Planned thyroidectomy (any extent) at a participating institution.
* Willing to undergo rapid 11-gene next-generation sequencing (NGS) panel and allow use of ultrasound DICOM images for AI analysis.

Exclusion Criteria

* Prior thyroid or major neck surgery.
* Known medullary thyroid carcinoma, anaplastic carcinoma, or metastatic disease outside the neck.
* Multiple endocrine neoplasia (MEN) syndromes or clinical suspicion of multi-gland disease.
* Pregnant or breastfeeding.
* Severe renal impairment (eGFR \< 30 mL/min/1.73 m²) or other condition that precludes surgery or gene testing.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Fujian Medical University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Bo Wang,MD

Director & Head of Thyroid Surgery, Principal Investigator, Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Fujian Medical University Union Hospital

Fuzhou, FJ, China

Site Status

Countries

Review the countries where the study has at least one active or historical site.

China

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Bo WANG, MD PhD

Role: CONTACT

+8613959123550

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Bo WANG, MD PhD

Role: primary

+8613959123550

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

RET-US

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.