A Liquid Biopsy for High-risk Pre-cancer Screening of Esophageal Adenocarcinoma
NCT ID: NCT06381583
Last Updated: 2024-05-10
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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COMPLETED
658 participants
OBSERVATIONAL
2023-04-15
2024-04-24
Brief Summary
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Detailed Description
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Non-invasive tests are more appealing to patients than invasive tests and can increase participation rates. Biomarker studies have shown promise, but existing tests lack sensitivity for early-stage EAC and, most importantly, to its precursor lesion BE. This is likely because they over-sampled analytes that are primarily expressed at the EAC end of the spectrum, but not in BE yet during the BE to EAC sequence.
This study proposes developing an innovative liquid biopsy test tailored for EAC and BE to address this. An ideal screening test should be minimally invasive, highly sensitive, and cost-effective. This test would optimize patient compliance and resource allocation by detecting both conditions from a single blood draw. More specifically, circulating microRNA (miRNA) analysis shows promise: tests based on cell-free microRNA (cf-miRNA) have demonstrated high sensitivity.
This study will develop a non-invasive blood test for BE and EAC in four phases:
1. In silico genome-wide profiling of tissue miRNA to select the best candidates for biomarker panels.
2. Prioritization of the biomarkers that are differentially expressed across the entire continuum of BE to EAC sequence, compared to the normal mucosa
3. Transition of these biomarkers to a liquid biopsy assay, confirming their detectability in blood as well as their differential expression in cases compared to controls
4. Utilizing machine learning to identify the most promising candidates and train algorithms for detecting EAC and BE, based on results from quantitative polymerase chain reaction (qPCR) analysis.
5. Independently validating these signatures using diverse cohorts to ensure broad applicability and compare the effectiveness of the blood assay to standard care through retrospective and prospective studies.
This study aims to develop a highly sensitive, specific, and cost-effective liquid biopsy for early detection of BE and EAC. Success could transform clinical practice by preventing EAC through early detection of pre-malignant lesions. Innovations include incorporating pre-malignant lesions into screening. This approach could potentially reduce EAC mortality and incidence and pave the way for new clinical trials.
Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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Patients with Esophageal Adenocarcinoma [Malignant Tissue]
Individuals who underwent endoscopy and were found to only have one of the following:
* Esophageal adenocarcinoma of any stage
* Esophageal adenocarcinoma confined to the mucosa (stage Tis)
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Patients with Esophageal Adenocarcinoma [Matching Normal Tissue]
Individuals who underwent endoscopy and were found to only have one of the following:
* Esophageal adenocarcinoma of any stage
* Esophageal adenocarcinoma confined to the mucosa (stage Tis)
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Patients with Esophageal Adenocarcinoma or High-Grade Dysplasia Barrett's Esophagus [Test Cohort]
Individuals who underwent endoscopy and were found to only have one of the following:
* Barrett's Esophagus, with high-grade dysplasia, independently of Barrett's segment length
* Esophageal adenocarcinoma of any stage
* Esophageal adenocarcinoma confined to the mucosa (stage Tis)
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Patients with Low-Grade Dysplasia or Long Segment Barrett's Esophagus [Test Cohort]
Individuals who underwent endoscopy and were found to only have Barrett's Esophagus, with one of the following:
* Craniocaudal maximal extension of 3 cm or more
* Low-grade dysplasia at most, independently of Barrett's segment length
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Individuals Without Esophageal Adenocarcinoma or Barrett's Esophagus [Test Cohort]
Individuals who underwent endoscopy and were found not to have any Barrett's Esophagus or adenocarcinoma.
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Patients with Esophageal Adenocarcinoma or High-Grade Dysplasia Barrett's Esophagus [Training]
Individuals who underwent endoscopy and were found to only have one of the following:
* Barrett's Esophagus, with high-grade dysplasia, independently of Barrett's segment length
* Esophageal adenocarcinoma of any stage
* Esophageal adenocarcinoma confined to the mucosa (stage Tis)
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Individuals Without Esophageal Adenocarcinoma or Barrett's Esophagus [Training Cohort]
Individuals who underwent endoscopy and were found not to have any Barrett's Esophagus or adenocarcinoma.
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Patients with Esophageal Adenocarcinoma or High-Grade Dysplasia Barrett's Esophagus [Validation]
Individuals who underwent endoscopy and were found to only have one of the following:
* Barrett's Esophagus, with high-grade dysplasia, independently of Barrett's segment length
* Esophageal adenocarcinoma of any stage
* Esophageal adenocarcinoma confined to the mucosa (stage Tis)
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Patients with Low-Grade Dysplasia or Long Segment Barrett's Esophagus [ValidationCohort]
Individuals who underwent endoscopy and were found to only have Barrett's Esophagus, with one of the following:
* Craniocaudal maximal extension of 3 cm or more
* Low-grade dysplasia at most, independently of Barrett's segment length
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Individuals Without Esophageal Adenocarcinoma or Barrett's Esophagus [Validation Cohort]
Individuals who underwent endoscopy and were found not to have any Barrett's Esophagus or adenocarcinoma.
EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Interventions
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EMERALD (Esophageal MicroRNAs for BaRRett's esophagus, Adenocarcinoma, and Dysplasia)
A panel of circulating microRNA, whose expression level is tested in cell-free derived samples.
Eligibility Criteria
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Inclusion Criteria
* Received standard diagnostic and staging (as necessary) procedures as per local guidelines, and at least one sample was drawn before receiving any curative-intent treatment.
* Received standard pathological and endoscopic diagnosis and assessment for cohort assignment.
Exclusion Criteria
* Short segment Barrett's esophagus with no evidence of dysplasia
* Ultra-short segment Barrett's esophagus with no evidence of dysplasia
18 Years
ALL
No
Sponsors
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City of Hope Medical Center
OTHER
Responsible Party
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Principal Investigators
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Ajay Goel, PhD
Role: PRINCIPAL_INVESTIGATOR
City of Hope Medical Center
Locations
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City of Hope Medical Center
Duarte, California, United States
Countries
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References
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Miyoshi J, Mannucci A, Scarpa M, Gao F, Toden S, Whitsett T, Inge LJ, Bremner RM, Takayama T, Cheng Y, Bottiglieri T, Nagtegaal ID, Shrubsole MJ, Zaidi AH, Wang X, Coleman HG, Anderson LA, Meltzer SJ, Goel A; FINBAR-EMERALD collaborative group. Liquid biopsy to identify Barrett's oesophagus, dysplasia and oesophageal adenocarcinoma: the EMERALD multicentre study. Gut. 2025 Jan 17;74(2):169-181. doi: 10.1136/gutjnl-2024-333364.
Other Identifiers
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23228/EMERALD
Identifier Type: -
Identifier Source: org_study_id
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