Efficacy and Prognosis of Microwave Ablation Treatment for Papillary Thyroid Microcarcinoma Assessed by Contrast-Enhanced Ultrasound Combined With Genetic and Molecular Diagnostics: A Prospective Observational Study

NCT ID: NCT07054229

Last Updated: 2025-07-08

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

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Recruitment Status

RECRUITING

Total Enrollment

480 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-01

Study Completion Date

2026-12-31

Brief Summary

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In 2016, there were 203,000 new cases of thyroid cancer in China, ranking 7th among all malignant tumours and 4th among women, and showing a rapid growth trend. Papillary thyroid cancer (PTMC) with a diameter of ≤10 mm is the most common type of thyroid cancer, accounting for about 50% to 60% of the total number of cases. Low-risk PTMC is the most common type of thyroid cancer, with low invasiveness and good prognosis. Surgery is the treatment of choice for low-risk PTMC, but it significantly affects the quality of life of patients by affecting the function of the thyroid gland and requiring long-term medication after surgery, as well as having a high incidence of intra- and postoperative complications; there are certain impacts and limitations in the actual treatment. Microwave ablation (MWA) is a therapeutic modality emerging in recent years, which has the characteristics of easy operation, precise positioning, safety and effectiveness, small postoperative damage, fast recovery, fewer complications, and does not affect the aesthetics of the patient, which not only avoids surgical trauma and reduces the anxiety of the patient, but also better preserves the function of the thyroid gland, and its clinical application is becoming more and more widespread. In recent years, the application of microwave ablation in the treatment of PTMC has received more and more attention. Ultrasound, as a first-line examination tool, is accepted by the majority of patients because of its advantages of safety, speed, efficiency, low price and painlessness. Contrast-enhanced ultrasound (CEUS) is a new examination technique developed in recent years, which can provide richer and clearer diagnostic information than conventional ultrasound and colour Doppler ultrasound. Ultrasound contrast agents (e.g. Sonovue, Sonazoid), Sonovue with sulphur hexafluoride microbubbles as the main ingredient and Sonazoid with perfluorobutane microbubbles as the main ingredient, are non-toxic, non-radioactive, do not require allergy testing, and do not have the advantages of liver or kidney toxicity, etc., and are increasingly recognised by the public. Ultrasonography is now widely used in clinical practice as the primary modality for assessing efficacy after thyroid ablation therapy. Molecular diagnosis is one of the most important tools for preoperative diagnosis and invasiveness assessment of thyroid cancer. Common thyroid cancer gene variants include point mutations such as BRAF V600E, RAS, TP53, PIK3CA, and gene integration variants such as CCDC6-RET and ETV6-NTRK3. This project intends to assess the efficacy and prognosis of microwave ablation therapy for micropapillary thyroid cancer by ultrasonography combined with genetic molecular diagnosis, which in turn will assist in clinical treatment decisions.

Detailed Description

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1.1 Background to the study 1.1.1 Overview of thyroid cancer

Thyroid cancer is the most prevalent malignancy of the endocrine system. Data from the National Cancer Centre show that:

203,000 new cases of thyroid cancer in China in 2016, ranking 7th among all malignant tumours and 4th among women, and showing a rapid growth trend. The most common pathological type of thyroid cancer is papillary thyroid carcinoma (PTC), which accounts for about 85%-90% of the total number of cases, followed by follicular thyroid carcinoma (FTC), medullary thyroid carcinoma (MTC), poorly differentiated thyroid carcinoma (PDTC) and undifferentiated carcinoma (ATC).

1.1.2 Overview of PTMC and its surgical treatment Papillary thyroid carcinoma (PTMC) refers to papillary carcinoma with a diameter of ≤10 mm, whose biological behaviour is relatively mild and disease-specific.

behaviour is relatively mild, and the disease-specific mortality rate is less than 1%. Surgery is currently the treatment of choice for PTMC, and studies have shown that the overall survival rates of PTMC at 10 and 15 years after surgery are 94.6% and 90.7%, respectively.

1.1.3 Clinical treatment of low-risk PTMC Surgery is the preferred treatment option for low-risk PTMC, but there are some disadvantages to surgical treatment, including: surgery affects the thyroid gland, and surgery is not recommended for low-risk PTMC.

These include: surgery affects the function of the thyroid gland and therefore requires long-term medication; there are certain complications during and after surgery; and it affects the quality of life of the patients.

However, surgical treatment also has some disadvantages, including: surgery affects the function of the thyroid gland and requires long-term medication after surgery; there are some complications during and after surgery; and it affects the quality of life of the patients.

Since the 1990s, a clinical study of active surveillance (AS) for low-risk PTMC has been conducted in Japan, and the results showed that it is an optional clinical management modality. However, this clinical management modality has not yet reached a consensus in China due to the uneven distribution of healthcare resources and the fact that patients may not always be in a position to undergo regular review and follow-up, which may lead to consequences such as delayed diagnosis and treatment, and patients' quality of life being affected by anxiety.

With the development of ultrasound and microwave technology, microwave ablation therapy is more and more widely used in papillary thyroid cancer. Studies have shown that microwave ablation therapy has the characteristics of easy operation, precise positioning, high safety, small postoperative damage, fast recovery, few complications and does not affect the aesthetics, which not only avoids the trauma of surgery and reduces the anxiety of patients, but also better preserves the function of the thyroid gland, and its clinical application is becoming more and more widespread.

1.1.4 Ultrasonography Ultrasound, as a first-line examination tool, is accepted by the majority of patients because of its safety, speed, efficiency, low price and painlessness.

It is accepted by the majority of patients. Contrast-enhanced ultrasound (CEUS) is a new examination technique developed in recent years, which can provide richer and clearer diagnostic information than conventional ultrasound and colour Doppler ultrasound. Ultrasound contrast agents (e.g. Sonovue, Sonazoid), Sonovue with sulphur hexafluoride microbubbles as the main ingredient and Sonazoid with perfluorobutane microbubbles as the main ingredient, are non-toxic, non-radioactive, do not require allergy testing, and do not have the advantages of liver or kidney toxicity, etc., and are increasingly recognised by the public. Ultrasonography is now widely used in clinical practice as the primary modality for assessing efficacy after thyroid ablation therapy.

1.1.5 Genetic molecular diagnosis Molecular diagnosis is one of the most important tools for preoperative diagnosis and invasiveness assessment of thyroid cancer. It is now known that the occurrence and development of thyroid cancer are associated with dozens of genetic variants. Common gene variants include BRAF V600E, RAS, TP53, PIK3CA and other point mutations, as well as CCDC6-RET, ETV6-NTRK3 and other gene integration variants.

According to TCGA data published in Nature in 2014, the proportion of PTC patients carrying 'high-risk' mutations such as TERT promoter and TP53 in Western populations is about 10-15%. In the Chinese population, the proportion of patients with 'high-risk' mutations is about 5%-10%, and they are more likely to have cervical lymph node metastasis. These patients may have a higher risk of recurrence or lymph node metastasis after ablative therapy, and ablative therapy is usually not recommended.

The WHO Thyroid Tumour Classification Overview (5th edition), published in 2022, suggests that thyroid cancers less than 1 cm should also be evaluated for aggressiveness in combination with genetic variants, and the Guidelines for the Diagnosis and Management of Thyroid Nodules and Differentiated Thyroid (2nd edition), published in 2023, clearly states that BRAF mutations in combination with mutations in genes such as TERT, PIK3CA, AKT1, and TP53 are indicative of a poor prognosis; any patient carrying BRAF mutations may have a higher risk of recurrence or lymph node metastasis. The Guidelines for the diagnosis and treatment of differentiated thyroid carcinoma (DTC), published in 2021, clearly state that BRAF mutations combined with TERT, PIK3CA, AKT1, TP53 and other mutations indicate a poor prognosis, and that any DTC (differentiated thyroid carcinoma) with a BRAF V600E/RAS mutation combined with TERT or TP53 mutations, or RAS combined with EIF1AX mutations is a 'high-risk' patient for postoperative recurrence.

The European ablation guidelines published in 2021 clearly list high-risk mutations (such as TERT promoter and TP53 mutations) as contraindications to ablation, and there is no relevant recommendation in the field of ablation therapy in China.

1.2 Risk/benefit evaluation This study is an observational, diagnostic study with no obvious potential risks to patients. Evaluating the efficacy and prognosis of microwave ablation therapy for micropapillary thyroid cancer by ultrasonography combined with genetic molecular diagnosis can effectively assist clinical decision-making.

1.2.1 Known potential risks Very few patients may have a potential risk of ultrasound contrast agent allergy.

1.2.2 Known potential benefits Evaluating the efficacy and prognosis of microwave ablation therapy for micropapillary thyroid cancer by ultrasonography combined with genetic molecular diagnosis can assess the risk of recurrent metastasis of the lesion and the presence or absence of recurrent metastasis, and can effectively assist clinical decision-making.

1.2.3 Evaluation of potential risk-benefit This study is a prospective, observational study with low risk and high benefit.

Conditions

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Microwave Ablation Contrast-enhanced Ultrasound Genetic and Molecular Diagnostics Papillary Thyroid Microcarcinoma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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The thyroid nodule was confirmed to be papillary thyroid microcarcinoma by fine-needle aspiration bi

1. Aged 18-70 years, gender not specified;
2. Patients with low-risk PTMC receiving initial treatment (meeting all the following criteria: single lesion with a maximum diameter ≤1cm; no cervical lymph node metastasis; no distant metastasis; no extrathyroidal extension; no family history of thyroid cancer; no history of head and neck radiation during childhood);
3. Patients who have undergone fine-needle aspiration cytology examination of thyroid nodules and 88-gene testing for thyroid cancer before surgery;
4. Patients voluntarily choose to undergo microwave ablation therapy or surgical resection.

Contrast enhanced Ultrasound

Intervention Type DRUG

Contrast Enhanced Ultrasound (CEUS) refers to the observation under ultrasound after the injection of ultrasound contrast agents, such as SonoVue or Lumason.

88-gene panel for thyroid cancer

Intervention Type GENETIC

"88-gene panel" refers to a testing combination that includes 88 genes, which are typically associated with the onset, progression, and prognosis of thyroid cancer.

Interventions

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Contrast enhanced Ultrasound

Contrast Enhanced Ultrasound (CEUS) refers to the observation under ultrasound after the injection of ultrasound contrast agents, such as SonoVue or Lumason.

Intervention Type DRUG

88-gene panel for thyroid cancer

"88-gene panel" refers to a testing combination that includes 88 genes, which are typically associated with the onset, progression, and prognosis of thyroid cancer.

Intervention Type GENETIC

Other Intervention Names

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CEUS

Eligibility Criteria

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Inclusion Criteria

* Aged 18-70 years, gender not specified;
* Patients with low-risk PTMC receiving initial treatment (meeting all the following conditions: single lesion with a maximum diameter ≤1cm; no cervical lymph node metastasis; no distant metastasis; no extrathyroidal extension; no family history of thyroid cancer; no history of head and neck radiation during childhood);
* Patients who have undergone fine-needle aspiration cytology examination of thyroid nodules and 88-gene panel testing for thyroid cancer before surgery;
* Patients voluntarily choose to undergo microwave ablation therapy or surgical resection.

Exclusion Criteria

* Tumor located in the isthmus of the thyroid;
* Pathological high-risk subtypes (tall cell subtype, columnar cell subtype, diffuse sclerosing subtype, solid/insular subtype, oncocytic subtype);
* Progressive enlargement of the cancer lesion in the short term (increase of more than 3mm within 6 months);
* Pregnant women, lactating women;
* Patients with severe coagulation disorders;
* Patients with contralateral vocal cord dysfunction;
* Patients with contraindications to ultrasound contrast agents;
* Other conditions deemed ineligible for enrollment by the investigator.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

OTHER

Sponsor Role lead

Responsible Party

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Qiyun Ou

Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Luo, Prof.

Role: STUDY_DIRECTOR

Department of Ultrasound in Medicine, Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Locations

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Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Guangzhou, Guangdong, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Ou, Dr.

Role: CONTACT

020-34071020

Facility Contacts

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Ou, Dr.

Role: primary

020-34071020

Other Identifiers

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SYSKY-2024-512-01

Identifier Type: -

Identifier Source: org_study_id

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