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Correlation Between Various Urinary Exosomal Protein Biomarkers and Pathological Manifestation in Thyroid Follicular Neoplasm: Early and Pre-operative Diagnosis of Follicular Thyroid Cancer

Correlation Between Various Urinary Exosomal Protein Biomarkers and Pathological Manifestation in Thyroid Follicular Neoplasm: Early and Pre-operative Diagnosis of Follicular Thyroid Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05463107
Enrollment
50
Registered
2022-07-18
Start date
2022-08-01
Completion date
2028-07-31
Last updated
2026-04-13

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

Conditions

Follicular Thyroid Cancer, Thyroid Cancer

Keywords

Exosome, Urine, Biological marker, Thyroglobulin, Galactin-3

Brief summary

Thyroid cancer is the most common endocrine malignancy in the world. Generally, thyroid cancer could be divided into well-differentiated and poorly-differentiated. Well-differentiated thyroid cancers usually have two different patterns, including papillary thyroid cancer and follicular thyroid cancer. Thyroid sonography is convenient to obtain repeatedly for the images of nodular goiter. However, cytology and pathology are still the golden rules to make the final diagnosis. Under the basis of sono-guided fine needle aspiration cytology, diagnosis of papillary thyroid cancer is typically using fine needle aspiration cytology based on the presentation of typical cytologic features. On the other hand, thyroid follicular lesion cannot be interpretated via cytology because the evidence of capsular invasion or vascular permeation of capsule will not be available in fine needle aspiration cytology. Surgical intervention with pathological specimens is the only pathway to make the final diagnosis. Interestingly, both patterns of well-differentiated thyroid cancer shared the same follow-up tumor marker, i.e. serum thyroglobulin. Up to date, pre-operative diagnosis of follicular thyroid cancer is still one of the unresolved issues in endocrine oncology.

Detailed description

Thyroid cancer is one of the most popular malignancy in the past several decades all over the world. For poorly-differentiated thyroid cancer, therapeutic strategy of costly target therapy together with immune therapy will be the pivotal one because of its poor prognosis. The average 5-year relative survival rate of anaplastic thyroid cancer is only 3 to 31 % on the stage from distant metastasis to localized disease. However, it will be very different for well-differentiated thyroid cancer, and the average 5-year relative survival rate of both thyroid papillary or follicular thyroid cancer is more than 98 %. Therefore, the most important treatment strategy for endocrinologists will consider the development of biomarkers for early diagnosis and postoperative follow-up, rather than measuring serum thyroglobulin alone, which is the only biomarker in the current medical guidelines, and there is no choice. Our research team tried to find the newer biomarker together with serum thyroglobulin for post-operative longitudinal follow-up of well-differentiated thyroid cancer in the past five years. The investigators used urinary exosomal proteins as target and did find several peptides to be helpful, including our published urinary exosomal thyroglobulin (UExTg). In Taiwan, goiter and thyroid cancer are prevalent diseases. Although papillary thyroid cancer could be diagnosed via reliable sono-guided fine needle aspiration cytology, follicular thyroid cancer is still an unresolved issue in daily medical practice, especially in cytology. the investigators need to find a practicably earlier biomarker, which should be convenient, non-invasive and repeatable in sample collection. In our previous research and published data, urine will be a reliable source of data. Exosomes are nano-vesicles, containing DNA, RNA and proteins, and usually secreted by cells into extracellular spaces. Generally, the vesicles of exosomes are only 40 to 150 nm in diameter. Exosomes may carry and transfer the messages between different tissues. Now, the existing evidences revealed that exosomes may represent certain messages from malignant cells, including diagnosed biomarkers or prognostic predictors. Previously, published data of exosomal studies in thyroid cancer focused on serum microRNA, long coding RNA and circular RNA, but only few published data on peptides, which were named as liquid biopsy. However, cell-secreted exosomes of malignancy could be collected not only in plasma, body fluid, but also from urine, which is the non-invasive pathway but valuable wastes of human body. Our research group had developed experienced technique to collect urinary exosomes via our pilot study in the past several years. Since the investigators proved the role of urinary exosomal thyroglobulin, UExTg, in post-operative follow-up in well-differentiated thyroid cancer in the past three years, from 2018-2020, the investigators also found several peptides to be the candidates of prognostic predictors in our preliminary studies, including Calprotectin A8/A9, Annexin-2, Angiopoietin-1.

Interventions

None listed

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* diagnosed patients with nodular goiter or multinodular goiter, thyroid papillary, follicular and anaplastic thyroid cancer, pre-operation.

Exclusion criteria

* unclearly diagnosed patients with thyroid papillary, follicular and anaplastic thyroid cancer

Design outcomes

Primary

MeasureTime frameDescription
Change of serum thyroglobulin levelWithin 36 monthsThyroid function test
Change of serum free T4 levelWithin 36 monthsThyroid function test
Change of serum TSH levelWithin 36 monthsThyroid function test
Change of anti-thyroglobulin levelWithin 36 monthsThyroid function test
Urinary exosomal thyroglobulin detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal galectin-3 detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal calprotectin A9 detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal transketolase detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal keratin 19 detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal angiopoietin-1 detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal tissue inhibitor of metalloproteinase detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal keratin 8 detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal calprotectin A8 detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal annexin II detectionWithin 36 monthsUrinary exosomal biomarker
Urinary exosomal afamin detectionWithin 36 monthsUrinary exosomal biomarker

Secondary

MeasureTime frameDescription
Thyroid fine needle aspiration cytologyWithin 36 monthsUrinary exosomal biomarker
Ultrasonography of thyroid nodulesWithin 36 monthsUrinary exosomal biomarker

Countries

Taiwan

Contacts

PRINCIPAL_INVESTIGATORCHIH-YUAN WANG, Doctor

Department of Internal Medicine, National Taiwan University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026