ctDNA Methylation Application in Postoperative Relapse and Adjuvant Chemotherapy Efficacy Evaluation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSinglera Genomics Inc.

About this trial

In this study, the investigators aimed to apply their previously developed multi-locus blood-based assay targeting circulating tumor DNA methylation to monitor postoperative relapse and evaluate adjuvant chemotherapy efficacy in resected stage I and stage II (without high risk) colorectal cancer after radical resection.

Eligibility criteria

Qualifiers

Patients must have histologically confirmed stage I/II (without high risk) colorectal cancer.

Male or female ≥ 18 years of age on the day of signing informed consent.

Patients need to receive surgical resection, and with ctDNA positive prior to resection of colorectal cancer (CRC).

Patients must have a performance status of ≤1 on the Eastern Cooperative Oncology Group (ECOG) Performance Scale.

Disqualifiers

Personal history of colorectal cancer, colorectal adenoma or aerodigestive tract cancer.

Induction of neoadjuvant systemic therapy prior to resection of CRC.

Patient is pregnant or lactating.

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.

Trial design

Treatments tested in this trial

  • a multi-locus blood-based assay

Treatment groups

2,000 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Singlera Genomics Inc.

Lead sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Collaborator