Endoscopic Versus Surgical Treatment for T1 Colorectal Cancer (EpiT1)

March 16, 2022 updated by: María Pellisé, Hospital Clinic of Barcelona

Endoscopic Versus Surgical Treatment for T1 Colorectal Cancer: a Population-based Cohort Study

The implementation of population screening programs for colorectal cancer (CRC) has led to a considerable increase in the prevalence T1 CRC originating on polyps amenable by endoscopy. The benefits of secondary oncological surgery in terms of disease free survival are not well established.

Hypothesis: The characteristics of the individuals and the polyp (endoscopic, histological) should allow us to discriminate T1 CRCs that may benefit from secondary surgery from those that only require local treatment. With the current criteria, the management of patients with T1 CRC is suboptimal since a high proportion of patients are refered for unnecessary surgeries without a clear benefit in terms of survival. Molecular signatures can help to discriminate those patients with good prognosis that do not require secondary surgery nor cancer related follow up.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

The primary objective of the study is to compare the effect of oncological surgery versus local treatment for the management of polyps with T1 CRC in relation to disease-free survival and morbi-mortality of the therapeutic procedure. We will also validate molecular signatures in endoscopic samples for the prediction of lymph node metastasis and survival. Methodology: Clinical Study: Retrospective population-based cohort study that will include baseline clinical and follow up data of more than 1400 T1 CRCs in at least 10 Spanish autonomous communities from 2007 to 2017. A centralized pathological review will be carried out by a group of expert pathologists. Inter and intraobserver variability for histological staging will be assessed. A predictive model will be created to discriminate individuals with high probability of receiving surgical and local treatment. For those patients who have a similar probability range, the results in progression-free survival and adverse events will be compared. Translational phase: A 5miRNAs and 8mRNA signature predictive of lymph node metastasis will be assessed in 200 endoscopic samples and related with prognosis.

Study Type

Observational

Enrollment (Anticipated)

1400

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Barcelona, Spain, 08036
        • María Pellisé. MD. PhD.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Spanish multicenter observational retrospective cohort study where all cases of pT1 CRC will be included from January 2007 to December 2017. Patients will be included both inside and outside the CCR national screening program.

Description

Inclusion Criteria:

- All patients diagnosed with pT1 CRC will be included, regardless of endoscopic features, treatment received and lymph node staging

Exclusion Criteria:

  • CRC with other histology than adenocarcinoma
  • Patients with hereditary syndromes of CRC (Lynch syndrome, classical familial adenomatous polyposis) or inflammatory bowel disease.
  • Synchronous CRC
  • Metachronous CRC in the previous 5 years
  • Patients with metastatic neoplastic disease at the time of diagnosis

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall survival
Time Frame: 1 year
Evaluate the effect of surgery and local (endoscopic) treatment on overall survival (expressed in months)
1 year
Disease free survival
Time Frame: 1 year
Evaluate the effect of surgery and local (endoscopic) treatment on disease free survival (expressed in months)
1 year
Develop a predictive model of the probability of receiving surgical treatment
Time Frame: 1 year
Determine factors associated with the choice of primary treatment and final treatment (endoscopic, primary surgery or secondary surgery) and to develop a predictive model that allow discriminate individuals with high probability of receiving surgical treatment
1 year
Validation of molecular signatures
Time Frame: 2 years
Evaluate the validity of molecular signatures based on mRNA and miRNA (determined in endoscopic samples) for prediction lymph node metastasis
2 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prognosis
Time Frame: 1 year
Determine the prognosis of patients with pT1CRC in relation to the treatment received (local, primary surgery or secondary surgery)
1 year
Risk of lymph node metastasis
Time Frame: 1 year
Evaluate the factors of the individual and the polyp that are associated with lymph node metastasis
1 year
Concordance of histological evaluation
Time Frame: 2 years
Evaluate the inter-intraexplorer concordance of the pathologists for the histological staging criteria.
2 years
T1 CRC in screening program
Time Frame: 1 year
Compare the characteristics of the T1 CRCs diagnosed within a population screening program and outside it.
1 year
Proportion of adverse events
Time Frame: 1 year
Evaluate the proportion of adverse effects after endoscopic or surgical treatment
1 year
Sensitivity and specificity of follow-up tests
Time Frame: 1 year
To evaluate the performances of the different tests (CT, US, blood markers, colonoscopy) during follow up for detecting recurrence
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2019

Primary Completion (Actual)

May 1, 2021

Study Completion (Anticipated)

December 31, 2022

Study Registration Dates

First Submitted

October 17, 2019

First Submitted That Met QC Criteria

October 31, 2019

First Posted (Actual)

November 4, 2019

Study Record Updates

Last Update Posted (Actual)

March 17, 2022

Last Update Submitted That Met QC Criteria

March 16, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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