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Clinical Trials/NCT05229341
NCT05229341RecruitingNot Applicable

Evaluation of DNA Methylation Signatures in Diagnosis and Management of Thyroid Nodules

City of Hope Medical Center1 site in 1 country1,450 target enrollmentStarted: October 22, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
1,450
Locations
1
Primary Endpoint
Positive predictive value (PPV) of DDMS-2

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

Diagnostic (needle biopsy, DDMS-2)

Experimental

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

Intervention: Diagnostic Procedure (Procedure)

Diagnostic (needle biopsy, DDMS-2)

Experimental

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

Intervention: Electronic Health Record Review (Other)

Diagnostic (needle biopsy, DDMS-2)

Experimental

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

Intervention: Needle Biopsy (Procedure)

Outcomes

Primary Outcomes

Positive predictive value (PPV) of DDMS-2

Time Frame: Up 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)

Time Frame: 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-2

Time Frame: Up 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-2

Time Frame: Up 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 Outcomes

No secondary outcomes reported

Investigators

Sponsor
City of Hope Medical Center
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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