Thyroid Cancer 16 Gene Mutations Detection Kit
Next Generation Sequencing
Thyroid Cancer 16 Gene Mutations Detection Kit
To assist in the differential diagnosis of benign and malignant thyroid nodules ; Prompt the risk of recurrence ; Guide the targeted therapy of thyroid carcinoma ; Prompt genetic risk.
BACKGROUND


Thyroid nodules can be found in various age groups. In the adult population, the incidence rate detected through physical examinations is approximately 5%-7%, while the incidence rate detected through ultrasound examination ranges from 20%-76%. Different pathological types of thyroid nodules (tumors) exhibit significant differences in their biological behavior. From benign thyroid adenomas and indeterminate thyroid nodules to thyroid carcinoma, these variations can have a profound impact on patient prognosis and treatment options.


AUXILIARY EXAMINATION AND DIAGNOSIS


Ultrasound: Ultrasound examination is simple and non-invasive, with high specificity and sensitivity for thyroid nodule detection.

Cytopathology Diagnosis Report: The Bethesda System is used for the reporting of cytopathology diagnosis.

Molecular Testing: To improve the accuracy and effectiveness of thyroid fine-needle aspiration (FNA) cytology diagnosis, molecular testing is recommended for III and IV category thyroid FNA specimens or Puncture eluent.


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NCCN Guidelines for Diagnosis and Treatment of Thyroid Carcinoma 2025.V1



Clinical Application of Gene Detection in Thyroid Carcinoma 



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Endocrinol Metab Clin North Am, 2019, 48(1):109-124.



DETECTED GENES 

This test adopts the high-throughput sequencing method and covers the genes related to the identification, prognosis and adjuvant treatment of thyroid tumors recommended in the NCCN guidelines, CSCO guidelines and expert consensus.

PRODUCT INFORMATION
Product Name
Core Technology
Pack Size
Instruments Validated
Sample Type
Thyroid Cancer 16 Gene Mutations Detection Kit
RingCap®
16 Tests/Kit; 32 Tests/Kit
Illumina, MGI, Sikun,etc.
Tumor tissue; FNA( Control sample(Whole blood, saliva, oral swab) is required for germ line detection)
APPLICABLE POPULATION

1.Patients with thyroid nodules with uncertain results diagnosed by US-FNA cytology ;

2.Patients undergoing surgical treatment, radioactive iodine therapy or ablation ;

3.Patients with advanced thyroid carcinoma to be selected for targeted therapy ;

4.Patients with hereditary MTC background and their families.

DETECTION SIGNIFICANCE

( 1 ) To assist the diagnosis of benign and malignant thyroid nodules and the classification of thyroid carcinoma.

( 2 ) To guide the choice of surgical plan.

( 3 ) Guidance of radioactive iodine therapy

( 4 ) Guiding targeted therapy

( 5 ) Assessing genetic risk


FEATURES & ADVANTAGES
Cost-effective

Cost-effective

Covering 16 core driver genes of thyroid carcinoma, assisting pathological diagnosis and subtype classification.

High Sensitivity

High Sensitivity

Gene mutations with frequencies as low as 1 % can be detected in 5 ng FNA samples or 25 ng tissue samples.

Leading Technology

Leading Technology

Using RingCap® independent patent technology, the database construction method is simple, the operation steps are few, and the turn around time is short.

Strong Compatibility

Strong Compatibility

Compatible with mainstream platforms on the market.

DETECTION PROCESS

1. Nucleic Acid Extraction

2. Library Preparation (3.5 hours total time)

3. Sequencing

4. Auto-data Analysis

5. Report