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NCT Number: NCT05463107

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

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Change of serum thyroglobulin level

    Time frame: Within 36 months

    Thyroid function test

  2. Change of serum free T4 level

    Time frame: Within 36 months

    Thyroid function test

  3. Change of serum TSH level

    Time frame: Within 36 months

    Thyroid function test

  4. Change of anti-thyroglobulin level

    Time frame: Within 36 months

    Thyroid function test

  5. Urinary exosomal thyroglobulin detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  6. Urinary exosomal galectin-3 detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  7. Urinary exosomal calprotectin A9 detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  8. Urinary exosomal transketolase detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  9. Urinary exosomal keratin 19 detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  10. Urinary exosomal angiopoietin-1 detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  11. Urinary exosomal tissue inhibitor of metalloproteinase detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  12. Urinary exosomal keratin 8 detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  13. Urinary exosomal calprotectin A8 detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  14. Urinary exosomal annexin II detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

  15. Urinary exosomal afamin detection

    Time frame: Within 36 months

    Urinary exosomal biomarker

Secondary outcomes

  1. Thyroid fine needle aspiration cytology

    Time frame: Within 36 months

    Urinary exosomal biomarker

  2. Ultrasonography of thyroid nodules

    Time frame: Within 36 months

    Urinary exosomal biomarker

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Important dates

Study start
2022
Primary completion
2026
Study completion
2028
First posted
Jul 18, 2022
Registry last updated
Apr 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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