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Evaluation of DNA Methylation Signatures for the Diagnosis and Management of Thyroid Nodules

Not Applicable
Recruiting
Conditions
Thyroid Gland Carcinoma
Interventions
Procedure: Diagnostic Procedure
Other: Electronic Health Record Review
Procedure: Needle Biopsy
Registration Number
NCT05229341
Lead Sponsor
City of Hope Medical Center
Brief Summary

This clinical trial evaluates deoxyribonucleic acid (DNA) methylation signatures in diagnosing and managing thyroid nodules. The purpose of this research is to develop a new test for thyroid cancer. This test will use needle biopsies (small collections of tissue with a needle) from the thyroid to determine whether the participant has a malignant (cancer) or benign (not showing cancer) thyroid tumor. The information learned from this trial may help develop a more accurate test so that patients do not have unnecessary surgeries for nodules that are thought to be suspicious but are actually benign.

Detailed Description

PRIMARY OBJECTIVE:

I. To evaluate the effect of Diagnostic DNA Methylation Signatures (DDMS-2) results (positive predictive value \[PPV\], negative predictive value \[NPV\], sensitivity and specificity) on physician decision-making for clinical management of 800 indeterminate thyroid nodules.

SECONDARY OBJECTIVES:

I. To determine sensitivity and specificity, PPV, NPV of DDMS-2 with 1450 needle biopsies including 800 needle biopsies with indeterminate cytopathology.

II. Compare the diagnostic accuracy between DDMS-2 and two currently used diagnostic approaches based on genetic alterations and gene expression within the same prospective cohort of 800 indeterminate needle biopsies.

OUTLINE:

Patients undergo needle biopsy for collection of tissue samples. Tissue samples are analyzed using DDMS-2. Patients' medical records are also reviewed.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1450
Inclusion Criteria
  • Patients without impaired decision-making capacity and who are undergoing needle biopsies for thyroid nodule diagnosis
  • Over the age of 18
  • Any gender, race and ethnicity
  • Patients must provide informed consent prior to use of their tissues and clinical data
Exclusion Criteria
  • Children are excluded from the study, since the biology of children thyroid nodules is different from adults

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Diagnostic (needle biopsy, DDMS-2)Diagnostic ProcedurePatients undergo needle biopsy for collection of tissue samples. Tissue samples are analyzed using DDMS-2. Patients' medical records are also reviewed.
Diagnostic (needle biopsy, DDMS-2)Electronic Health Record ReviewPatients undergo needle biopsy for collection of tissue samples. Tissue samples are analyzed using DDMS-2. Patients' medical records are also reviewed.
Diagnostic (needle biopsy, DDMS-2)Needle BiopsyPatients undergo needle biopsy for collection of tissue samples. Tissue samples are analyzed using DDMS-2. Patients' medical records are also reviewed.
Primary Outcome Measures
NameTimeMethod
Positive predictive value (PPV) of DDMS-2Up to 5 years

PPV (number of true thyroid cancer specimens by DDMS / number of thyroid cancers diagnosis by DDMS) will be calculated. Will also determine the 95% confidence intervals.

Sensitivity of Diagnostic Deoxyribonucleic Acid (DNA) Methylation Signatures (DDMS-2)Up to 5 years

The sensitivity of DDMS-2 will be estimated by taking the ratio of the number of true thyroid cancer specimens diagnosed as cancer by DDMS and the total number of thyroid cancer specimens. Will also determine the 95% confidence intervals.

Specificity of DDMS-2Up to 5 years

The specificity will be estimated by taking the ratio of the number of true benign nodules diagnosed as benign by DDMS and the total number of true benign thyroid nodules. Will also determine the 95% confidence intervals.

Negative predictive value (NPV) of DDMS-2Up to 5 years

NPV (number of true benign nodules diagnosed by DDMS/number of benign diagnosis by DDMS) will be calculated. Will also determine the 95% confidence intervals.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

City of Hope Medical Center

🇺🇸

Duarte, California, United States

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