Prediction of Lymph Node Metastasis in Patients With Thyroid Malignancy by a New Scale

Quantitative Rating Scale Based on Preoperative Prediction of Lymph Node Dissection in Patients With Thyroid Cancer

The incidence of papillary thyroid cancer (PTC) has been on the rise in recent years, and 20%-50% of PTC patients will have lymph node metastasis. Lymph node involvement in PTC patients is usually related to the recurrence of PTC after surgery, and 30% of patients recur without lymph node dissection, with the risk of central cervical lymph node metastasis being the greatest, so it seems to be a good choice to perform lymph node dissection on patients after thyroidectomy, but in fact, there are controversies at home and abroad as to whether to perform lymph node dissection or not. The 2021 Chinese Society of Clinical Oncology (CSCO) guidelines for the diagnosis and treatment of differentiated thyroid cancer state that prophylactic central lymph node dissection (PCND) may increase the incidence of postoperative complications, but due to the high metastatic rate of PTC and the ability of PCND to effectively prevent recurrence and reoperation, countries in the East Asian region perform prophylactic lymph node dissection on almost all patients with PTC. However, for more countries in Europe and the United States, performing PCND has become a non-essential, individualized option. The aim of this study is to collect multifactorial data from more than 1,000 patients who have undergone previous thyroidectomy from 2021 to 2023, and to develop a novel scoring scale that can be used to individualize patients' scores based on a variety of factors prior to surgery, so that patients can be more accurately predicted to have lymph node metastasis and need prophylactic lymph node dissection prior to surgery, and patients who do not need dissection can avoid surgery. For patients who do not need lymph node dissection, complications caused by surgery can be avoided, while for patients who do have lymph node metastasis, recurrence of their cancer can be prevented. This will change the status quo of not being able to accurately determine the actual situation through simple preoperative examination or performing prophylactic lymph node dissection for all PTC patients.

Study Overview

Status

Recruiting

Detailed Description

1. Patient characteristics: the inclusion criteria were as follows:1. patients with papillary thyroid cancer;2. minimum age of 16 years old and maximum age of 80 years old. Exclusion criteria:1. age less than 16 years old;2. postoperative pathology suggesting that there are other types of tumors, such as medullary carcinoma or undifferentiated carcinoma. 2,.Data collection: Investigators collected multifactorial data on about 1000 patients who had undergone previous thyroidectomy from 2021-2023, including gender, height, age, weight, BMI, diameter of the tumor in the primary focus, tumor limitation in the primary focus, lymph node metastasis, and tumor invasion, preoperative ultrasonographic manifestations, preoperative laboratory results, pathological results, and genetic testing results. From these, the available data were screened and retained for analysis. 3.Data analysis: According to the retained data after screening, classical machine learning algorithms will be used for feature selection to select the factors with greater correlation with the results, and then with the help of data visualization, the specific quantitative relationship between each factor and the results will be determined according to the distribution of the available data, and the quantitative scoring table will be created. 4. Clinical validation: The completed quantitative rating scale investigators will be validated in the clinic. Investigators will use the scale to score new patients to assess whether participants need prophylactic lymph node dissection, and then evaluate the accuracy of the quantitative scale according to the intraoperative or postoperative situation.

Study Type

Observational

Enrollment (Estimated)

800

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Shaanxi
      • Xi'an, Shaanxi, China, 710000
        • Recruiting
        • The Second Affiliated Hospital of Xi'an Jiaotong University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

From 2021 to 2023, 500 patients with previous papillary thyroid cancer surgery were selected at the Second Affiliated Hospital of Xi'an Jiaotong University for the quantitative rating scale, as well as 300 newly admitted papillary thyroid cancer patients for subsequent validation.

Description

Inclusion Criteria:

  • Papillary thyroid cancer
  • Conscious and able to communicate normally
  • Age 16-80 years

Exclusion Criteria:

  • Preoperative or postoperative pathology suggests other types of tumors, such as medullary carcinoma or undifferentiated carcinoma.
  • Less than 16 years of age

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Past Medical Records Group
Sample size:500 Whether control group:No Name of exposure factor:papillary thyroid cancer Exposure factor type:Other Description of exposure factor:None
Clinical Validation Group
Sample size:300 Whether control group:No Name of exposure factor:papillary thyroid cancer Exposure factor type:Other Description of exposure factor:None

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Height
Time Frame: up to three years
The height indicator will summarize the data in "meters".
up to three years
Weight
Time Frame: up to three years
The weight indicator will summarize data in "kilograms".
up to three years
Age
Time Frame: up to three years
Age will be aggregated using "years" as the unit of measurement.
up to three years
Genders
Time Frame: up to three years
Data will be summarized in terms of "male" and "female" as units of measurement.
up to three years
BMI
Time Frame: up to three years
BMI will be summarized in "kg/m^2".
up to three years
Whether lymph node dissection was performed during previous surgery
Time Frame: up to three years
Data will be summarized using "yes" or "no" for whether lymph node dissection was performed during previous surgery.
up to three years
Tumor Diameter Size
Time Frame: up to three years
Tumor diameter size will be summarized in "millimeters".
up to three years
Tumor limitation of the primary focus
Time Frame: up to three years
Tumor limitation of primary foci will be summarized using "single/multiple" and "unilateral/bilateral".
up to three years
Extratumoral invasion
Time Frame: up to three years
Extra-tumor focal invasion will be summarized with a "yes" or "no" to the data.
up to three years
Pathologic lymph node metastasis
Time Frame: up to three years
Pathological lymph node metastases will be summarized with "yes" or "no" data.
up to three years
Tumor cystic solidity on preoperative ultrasound
Time Frame: up to three years
Pre-operative ultrasound tumor cysticity will be summarized as "cystic" or "solid".
up to three years
Preoperative ultrasound tumor echo intensity
Time Frame: up to three years
Preoperative ultrasound tumor echo intensity will be summarized as "high echo" or "moderate echo" or "low echo" or "very low echo".
up to three years
Preoperative ultrasound tumor boundaries
Time Frame: up to three years
Preoperative ultrasound tumor boundaries will be summarized as "clear" or "unclear".
up to three years
Preoperative ultrasound tumor for the presence of calcifications
Time Frame: up to three years
Preoperative ultrasound tumors will be summarized with "yes" or "no" for the presence of calcifications.
up to three years
Preoperative ultrasound tumor aspect ratios
Time Frame: up to three years
Preoperative ultrasound tumor aspect ratios will be summarized with ">1" or "<1" data
up to three years
Preoperative ultrasound for enlarged cervical lymph nodes
Time Frame: up to three years
Preoperative ultrasound of cervical lymph nodes for enlargement will be summarized as "yes" or "no".
up to three years
TSH
Time Frame: up to three years
The TSH indicator will summarize data in "mlU/L".
up to three years
TPOAb
Time Frame: up to three years
The TPOAb indicator will summarize data in "lU/mL".
up to three years
TgAb
Time Frame: up to three years
The TgAb indicator will summarize data in "lU/mL".
up to three years
Calcium
Time Frame: up to three years
The Calcium indicator will summarize data in "mmol/L".
up to three years
B-raf gene mutation
Time Frame: up to three years
B-raf mutations will be summarized as "wild type" or "mutant".
up to three years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2023

Primary Completion (Estimated)

October 1, 2025

Study Completion (Estimated)

October 1, 2026

Study Registration Dates

First Submitted

February 7, 2024

First Submitted That Met QC Criteria

February 22, 2024

First Posted (Estimated)

February 29, 2024

Study Record Updates

Last Update Posted (Estimated)

February 29, 2024

Last Update Submitted That Met QC Criteria

February 22, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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