Plasma 5hmC Signatures as a Marker of Colorectal / Appendiceal Peritoneal Metastasis
NCT ID: NCT04157322
Last Updated: 2025-12-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
55 participants
OBSERVATIONAL
2019-08-26
2027-10-31
Brief Summary
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Detailed Description
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* Just before surgery (During the preoperative clinic visit or at the operating room).
* 5-7 days after surgery (just before hospital discharge).
* 6 weeks after surgery (first postoperative clinic visit).
* 3 months after surgery (second postoperative clinic visit).
* 6 months after surgery (third postoperative clinic visit).
* 9 months after surgery (fourth postoperative clinic visit).
* 12 months after surgery (fifth postoperative clinic visit). Standard of care surveillance elements that include patient history and physical examination, conventional blood biomarkers (CEA, CA 19-9 and CA 125) and cross sectional imaging of the chest, abdomen and pelvis will be undertaken simultaneously at similar time points. We will then compare the sensitivities of DNA hydroxymethylation signatures and conventional blood biomarkers in diagnosing clinically detectable recurrence at 1 year after surgery. We hypothesize that plasma hydroxymethylation signatures have higher sensitivity in identifying clinically detectable recurrence when compared with conventional tumor markers (CEA, CA 19-9 and CA 125).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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prospective single arm biomarker (plasma cell-free DNA hydroxymethylation) study
Blood draw
Eligibility Criteria
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Inclusion Criteria
II. Age ≥ 18 years. III. Patients with known peritoneal metastasis (PM) who are candidates for complete cytoreduction and HIPEC. Known PM - diagnosed previously by diagnostic laparoscopy / laparotomy or clear radiological evidence of PM.
IV. Neoadjuvant chemotherapy permitted. V. The patient is able to provide informed consent. VI. The patient is planned to undergo his / her postoperative surveillance at UCM, as this study's protocol requires multiple clinic visits.
VII. No evidence of systemic metastasis.
\-
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of Chicago
OTHER
Responsible Party
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Principal Investigators
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Bruce Bissonnette, MD
Role: PRINCIPAL_INVESTIGATOR
University of Chicago
Locations
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The University of Chicago
Chicago, Illinois, United States
Countries
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Other Identifiers
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IRB19-0913
Identifier Type: -
Identifier Source: org_study_id
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