MedPath

Detection of Breast Cancer With Non-invasive Method Based on DNA Methylation of Circulated Tumor DNA, PBMC

Terminated
Conditions
Breast Cancer
Breast Cancer Female
Registration Number
NCT03480659
Lead Sponsor
HKGepitherapeutics
Brief Summary

A central challenge in the fight against breast cancer is how to detect disease in a noninvasive manner before it is detectable by imaging methods. Although inroads have been made with more sensitive imaging techniques for earlier detection of breast cancer, these techniques are limited by the size of lesion that could be detected. Alternatively, several blood proteomic biomarkers have been proposed but none offer as of yet sufficient predictive power. Consequently, effective non-invasive tools as prognostic indicators and biomarkers of breast cancer are urgently needed.

The purpose of this study is to develop and test non-invasive biomarkers based on methylation changes in PBMC and circulated tumor DNA in breast cancer patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
165
Inclusion Criteria
  • Histological confirmed breast cancer subtypes (DCIS and invasive)
Exclusion Criteria
  • Pregnant women
  • Minors (subjects less than 18 years of age)
  • Prisoners
  • Patients with known infectious disease, such as human immunodeficiency virus (HIV), tuberculosis (TB), or hepatitis B, C
  • Patients having other than one cancer
  • Subjects unable to consent for themselves

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
DNA methylation of circulated tumor and PBMC DNA and its Correlation to Development and prediction of breast cancer6 months to 1 year

We will develop the linear model and a threshold value differentiating breast cancer from control based on the 100 patient training set. The model will be provided to the researchers:

Methylation score=CG1\*b1+CG2\*b2+ CG3\*b3 + e

CG1 is the methylation value of the first CG b1 is the regression coefficient for the first CG and e equals the intercept.

We will develop the regression coefficient and intercept as well as the DNA methylation values for each patient for each CG. We will first compute the polygenic methylation score for each patient. Then based on the computer threshold based on the training cohort will call the samples as breast cancer or not.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Kazakh Institute of Oncology and Radiology

🇰🇿

Almaty, Kazakhstan

© Copyright 2025. All Rights Reserved by MedPath