Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06314958

Stage II/III Colorectal Cancer Recurrence

This study will develop an assay to predict disease recurrence in patients with stage II/III CRC after receiving adjuvant chemotherapy, using genome-wide DNA methylation.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Second Affiliated Hospital of Dalian Medical University, Dalian, China

Loading trial locations.

About this study

Adjuvant chemotherapy (ACT) is the standard clinical care for patients with stage III or high-risk stage II colorectal cancer (CRC) after curative-intent resection. Nonetheless, more than 30% of patients experience CRC recurrence. Accurate prediction of recurrence risk in stage II/III CRC patients who undergo ACT is crucial for determining the necessity and duration of ACT, as well as for tailoring novel treatment strategies for these patients.

This study will comprise three phases

  • A systematic and comprehensive CpG methylation-based epigenetic biomarker discovery phase to identify the differentially methylated CpG sites associated with recurrence-free survival (RFS) < 5 years and > 5 years. In this phase, LASSO-based machine learning algorithms will be used to optimize the biomarker candidates.
  • A tissue-based clinical assay development phase by quantitative pyrosequencing
  • An independent validation phase.

At completion, this study will validate a tissue-based assay to predict the development of recurrence after the completion of chemotherapy in patients with stage III and II CRC

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Stage II (high-risk) or III colorectal cancer (TNM classification, 8th edition).
  • Received standard diagnostic, staging, and therapeutic procedures as per local guidelines
  • Received stage-specific curative-intent resection followed by adjuvant chemotherapy.
  • Confirmed cancer-free survivorship confirmed at the time of study inclusion.

Exclusion criteria

  • Lack of written informed consent.
  • Development of recurrence in the first 6 months following adjuvant chemotherapy completion.
  • Hereditary colorectal cancer syndromes (identified through genetic testing)
  • Inflammatory bowel diseases

Treatment and study plan

CENSURE

Other

A panel of CpG sites, whose methylation level is tested in macro-dissected formalin-fixed and paraffin-embedded (FFPE) samples derived from the primary tumor.

Other names: CENSURE (CpG mEthylation-based epigeNetic SignatURE)

Primary outcomes

  1. Recurrence-Free Survival

    Time frame: Up to 120 months

    Time from treatment completion to development of recurrence (or death)

Secondary outcomes

  1. Overall Survival

    Time frame: Up to 120 months

    Time from treatment completion to death from any cause

Study contacts

Contact information is provided by the study sponsor or research team.

Ajay Goel, PhD

CONTACT

[email protected]

6262183452

Sponsors and collaborators

Lead sponsor

City of Hope Medical Center

Other

Registry information

Official study title

Predicting Recurrence-Free Survival in Stage III and High-Risk Stage II Colorectal Cancer After Curative-Intent Treatment

Acronym: CENSURE

Important dates

Study start
2023
Primary completion
2028
Study completion
2028
First posted
Mar 18, 2024
Registry last updated
Jul 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.