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Use of Plasma ctDNA Methylation Haplotypes in Detecting Local Residual or Lymph Node Metastasis

Use of Plasma ctDNA Methylation Haplotypes in Detecting Local Residual or Lymph Node Metastasis: a Prospective, Clinical Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03868215
Enrollment
100
Registered
2019-03-11
Start date
2018-05-01
Completion date
2020-08-31
Last updated
2019-03-11

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

Conditions

Colorectal Cancer, Lymph Node Metastases

Keywords

Colorectal Cancer, Lymph Node Metastases, Local Residual

Brief summary

This is a prospective, clinical study. This study is to evaluate the sensitivity of plasma ctDNA methylation haplotypes in detecting local residual or lymph node metastasis.

Detailed description

Colorectal cancer (CRC) is the third most common cancer worldwide, the second deadliest cancer in the United States. DNA methylation is a commonly used biomarker for non-invasive CRC detection in plasma. The low sensitivity of blood-based tests is due to several limitations of detecting ctDNA in early-stage cancer. We developed and validated a high-throughput methylation-based blood test highly sensitive for colorectal cancer and precancerous lesions. This previously established colorectal tumor-specific plasma ctDNA methylation markers (diagnostic model established by next-generation sequencing of 2181 gene loci methylation) had a high sensitivity in CRC patients and a high specificity in healthy individuals in a large retrospective sample study. This prospective, clinical study is to further evaluate the sensitivity of plasma ctDNA methylation haplotypes in detecting local residual or lymph node metastasis.

Interventions

NGS test for colorectal tumor-specific plasma ctDNA methylation markers prior to endoscopy and before surgical resection.

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with endoscopically removed malignant polyps. * Male or female ≥ 18 years of age on the day of signing informed consent. * Patients who received surgical resection following removal of malignant polyps by colonoscopy. * Patients must have a performance status of ≤1 on the ECOG Performance Scale. * Written informed consent must be obtained from patient or patient's legal representative and ability for patient to comply with the requirements of the study

Exclusion criteria

* Patients received adjuvant treatment prior to the surgical resection. * Patients received blood transfusion two weeks before or during the surgical resection. * Patients with unresected advanced colorectal adenoma. * Patients who are positive for Human Immunodeficiency Virus (HIV), Hepatitis B or Hepatitis C. * Patients who are pregnant. * Patients who are alcoholic or drug abusers. * Patients with a history or current evidence of any condition or abnormality that might confound the results of the study, interfere with the patient's participation for the full duration of the study, or is not in the best interest of the patient to participate, in the opinion of the Investigator.

Design outcomes

Primary

MeasureTime frameDescription
Sensitivity2 yearsThe sensitivity of plasma ctDNA methylation haplotypes in detecting local residual or lymph node metastasis

Countries

China

Contacts

Primary ContactGuoxiang Cai, M.D. Ph.D.
gxcai@fudan.edu.cn+86 13611831623

Outcome results

None listed

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