Integrating Tumor Genomics and Urinary Exosomal Proteomics to Establish a Multi-Layer Biomarker Framework for Early Risk Stratification and Post-Treatment Surveillance in Fresh Thyroid Cancer Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorNational Taiwan University Hospital

About this trial

Thyroid cancer is the most common endocrine malignancy, and although differentiated thyroid cancer (DTC) generally confers favorable outcomes, 10-20% of patients still face substantial postoperative risks, including local recurrence, distant metastasis, and inadequate response to radioactive iodine therapy. Current risk stratification, largely based on tumor size, lymph node involvement, and histopathology, fails to adequately represent tumor heterogeneity and evolutionary changes, potentially resulting in both overtreatment and undertreatment. Next-generation sequencing (NGS) has revealed a stepwise accumulation of genomic alterations from early driver mutations (e.g., BRAF, RAS, RET/PTC, PAX8-PPARG) to late-stage progression events (e.g., TERT promoter, TP53, PI3K/AKT/mTOR), while metastatic lesions often harbor high-risk mutations absent in primary tumors, underscoring the limitations of single-time-point tissue sampling. Furthermore, serum thyroglobulin (Tg) surveillance is hindered in patients with anti-Tg antibodies. Extracellular vesicles (EVs), particularly those obtained from urine, provide a compelling liquid biopsy modality due to their non-invasiveness, repeatability, and reduced interference by abundant serum proteins. The investigators' previous findings demonstrate that urinary exosomal peptides-including U-Ex Tg, ANXA2, TIMP, and Angiopoietin-1-correlate with malignancy, capsular invasion, and nodal metastasis, and exhibit dynamic postoperative variation, suggesting their utility in detecting molecular residual disease.

This prospective study will recruit 100 fresh thyroid cancer cases and integrate tumor genomic profiling, urinary exosomal proteomics via LC-MRM/MS, and clinical phenotype assessment-including nodal involvement, subsequent therapies, and long-term outcomes-to delineate causal links between genomic drivers, proteomic execution signals, and clinical progression. The overarching aim is to establish an early risk-stratification and molecular recurrence-alerting model capable of identifying high-risk trajectories earlier than conventional approaches, thereby enhancing surveillance precision and enabling timely intervention. This multi-layered biomarker framework holds strong potential to redefine postoperative monitoring standards and advance the clinical and policy implementation of precision medicine in thyroid cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 18 to 80 years

Newly diagnosed Papillary Thyroid Carcinoma (PTC) or highly suspected follicular thyroid neoplasms (including lesions with potential progression to poorly differentiated thyroid carcinoma)

Pre-operative status

Disqualifiers

Aged <18 or >80 years

No confirmed diagnosis of Papillary Thyroid Carcinoma (PTC)

No highly suspected follicular thyroid neoplasms (including lesions with potential progression to poorly differentiated thyroid carcinoma)

Trial population

Prospectively initiating enroll 100 newly diagnosed Differentiated thyroid cancer (DTC) patients undergoing surgery using standardized SOPs. Perform fresh-tissue next-generation sequencing (NGS) using a thyroid cancer-specific gene fusion/mutation panel. Collect paired urine samples preoperatively and at postoperative status according to a harmonized sampling schedule.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Change of serum thyroglobulin level

Thyroid function test

Time frame
Within 12 months
2

Change of serum free T4 level

Thyroid function test

Time frame
Within 12 months
3

Change of serum TSH level

Thyroid function test

Time frame
Within 12 months
4

Change of anti-thyroglobulin level

Thyroid function test

Time frame
Within 12 months

Secondary outcomes

1

Thyroid fine needle aspiration cytology

Thyroid function test

Time frame
Within 12 months
2

Ultrasonography of thyroid nodules

Thyroid function test

Time frame
Within 12 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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