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Clinical Trials/NCT03181490
NCT03181490
Completed
Not Applicable

Multi-centers Validation of a Circulating Tumor DNA Assay to Differentiate Benign and Malignant Pulmonary Nodules Via Targeted High-throughput DNA Methylation Sequencing

The First Affiliated Hospital of Guangzhou Medical University14 sites in 1 country1,490 target enrollmentJune 8, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pulmonary Nodule, Solitary
Sponsor
The First Affiliated Hospital of Guangzhou Medical University
Enrollment
1490
Locations
14
Primary Endpoint
The diagnostic performance of the blood-based assay for differentiating benign and malignant pulmonary nodules early using circulating tumor DNA (ctDNA) methylation analysis by next-generation sequencing (NGS)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Current state-of-the-art lung cancer early screening utilizes low-dose CT scan to identify lung nodules smaller than 3 cm in diameter. However, it's still a clinical challenge to differentiate between malignant and benign nodules.

In previous studies, the investigators had taken the approach of methylation profiling by high throughput bisulfite DNA sequencing in tissue samples to identify specific methylation signatures. The investigators had learned methylation patterns that differentiate malignant vs. benign lesions from tissue samples by in-depth data mining, and then used pattern matching to classify plasma samples.

In this study, the investigators are going to validate the efficacy of ctDNA methylation test for diagnosing early lung cancer by comparing results of the pre-surgery ctDNA methylation test with the post-surgery pathology.

Detailed Description

This is a prospective, multi-center, observational cohort study and seeks to enroll 1230 participants with pulmonary nodules 5-30mm in diameter. The assay analyzes the ctDNA methylation profiles of lung cancer-specific biomarkers non-invasively using whole blood specimens collected before invasive surgery. The performance characteristics(sensitivity and specificity) of the pre-surgery ctDNA methylation test for detection of early lung cancer is evaluated in comparison to post-surgery pathology.

Registry
clinicaltrials.gov
Start Date
June 8, 2017
End Date
May 31, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
The First Affiliated Hospital of Guangzhou Medical University
Responsible Party
Principal Investigator
Principal Investigator

Jianxing He

Principle Investigator

The First Affiliated Hospital of Guangzhou Medical University

Eligibility Criteria

Inclusion Criteria

  • 18 years old or above
  • single pulmonary nodule found by CT scan.
  • the diameter of the pulmonary nodule is between 5mm to 30mm.
  • plan to accept pneumonectomy due to the pulmonary nodule.
  • without any sign of lymphatic or distant metastasis.
  • agree to sign informed consent.

Exclusion Criteria

  • pregnant or lactating women.
  • the diameter of the pulmonary nodule is more than 30mm
  • there are 2 or more pulmonary nodules in one single patient.
  • any sign of lymphatic or distant metastasis

Outcomes

Primary Outcomes

The diagnostic performance of the blood-based assay for differentiating benign and malignant pulmonary nodules early using circulating tumor DNA (ctDNA) methylation analysis by next-generation sequencing (NGS)

Time Frame: 1 year

The efficacy of the blood-based ctDNA methylation assay comparing with pathologic diagnosis, the gold standard, including sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV).

Study Sites (14)

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