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Clinical Study of Glycosylated Extracellular Vesicles for Early Diagnosis of Breast Cancer

miRNAs of Circulating Glycosylated Extracellular Vesicles as Biomarkers for Early Diagnosis of Breast Cancer Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05417048
Enrollment
420
Registered
2022-06-14
Start date
2022-07-14
Completion date
2024-06-15
Last updated
2023-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Brief summary

This is a prospective, single-center, non-randomized, cohort study designed to evaluate the clinical diagnostic performance of glycosylated extracellular vesicles and their contents for early detection of breast cancer.

Detailed description

Early screening technology can improve the survival rate of breast cancer patients. Traditional mammography and ultrasonography have limitations on performance in clinical practice. Extracellular vesicles, one of the three major resources of liquid biopsy, contain multi-omics information that can be used to discover effective biomarkers for early diagnosis and screening of cancers. In this study, we are going to isolate glycosylated extracellular vesicles from serum of cancer patients and non-cancer people with the novel GlyExo-Capture technology, and perform miRNA sequencing to selected out breast cancer-related markers. Then an early diagnosis model of breast cancer based on the GlyExo-Capture platform is able to be established using machine learning techniques and validated by qPCR experiments.

Interventions

DIAGNOSTIC_TESTBlood Sample

Up to 5mL of blood via venipuncture

Sponsors

Beijing Glyexo Gene Technology Co., Ltd.
CollaboratorUNKNOWN
Peking University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Patients≥18 years old; 2. Histologically confirmed breast cancer patients,Benign breast disease (ig. breast fibroma, intraductal papilloma,mammary hyperplasia, breast cyst)or No breast lesions detected by clinical examination/mammography/ultrasound/breast magnetic resonance imaging (MRI) 3. Previous not received preoperative radiotherapy, chemotherapy, endocrine therapy, immunotherapy, or other anticancer treatments. 4. Subjects signed informed consent;

Exclusion criteria

1. A history of prior or concomitant malignancies; 2. advanced stage breast cancer (stage IV); 3. Patients were accompanied by severe organic diseases such as heart and cerebral disease, and liver and kidney disease.; 4. Pregnant or lactating women ; 5. Suspected or confirmed lesion was surgically removed; 6. Patients with incomplete clinical data; 7. Patients with poor compliance; 8. Patients with severe mental illness; 9. Patients had received blood transfusions during one month一;

Design outcomes

Primary

MeasureTime frameDescription
The diagnostic performance of the blood assay for differentiating benign and malignant breast disease using glycosylated extracellular vesicles analysis24 monthsThe efficacy of the blood-based assay comparing with patholgic diagnosis, the gold standard, and imaging diagnosis, including sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV)

Countries

China

Contacts

Primary ContactZhaoqing Fan, MD
zhqfan@sina.com+86-10-88197838

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026