Use of iFOBT in Patients Presenting With Alarm Symptoms of Colorectal Cancer

February 28, 2020 updated by: University of Aarhus

Use of the Immunochemical Faecal Occult Blood Test (iFOBT) in Patients Presenting With Alarm Symptoms and Referred to Colonoscopy in the Cancer Patient Pathway for Colorectal Cancer

Background: Colorectal cancer (CRC) is one of the most common types of cancer in Denmark, and mortality among patients is high. Patients presenting with alarm symptoms of CRC are referred to colonoscopy in the cancer patient pathway for CRC. However, the proportion of patients with alarm symptoms who have CRC is below 10%. Simultaneously, the burden on endoscopy units to conduct fast-track colonoscopies is growing.

Occult blood in the faeces may be an early sign of cancer or precancerous lesions, and can be detected by an immunochemical faecal occult blood test (iFOBT). Few studies have examined the diagnostic properties of the iFOBT among symptomatic patients, and reported sensitivities ranging from 88%-100%, specificities from 77%-94%, and negative predictive values from 98%-100%. These results were derived from diverse patient populations, and used different cut-offs to define positive test results. Using iFOBT may be a valuable tool for the GP when deciding on referral of the patient to the cancer patient pathway. However, evidence is needed on the diagnostic accuracy of the test to detect CRC among patients presenting with alarm symptoms.

Hypothesis: In patients presenting with alarm symptoms of CRC, detection of faecal occult blood by iFOBT is an accurate measure of the presence of colonic lesions.

Aim: The aim of the study is to examine the diagnostic accuracy of the iFOBT among symptomatic patients referred to colonoscopy in the cancer patient pathway for CRC.

Materials and methods: The project is conducted as a diagnostic accuracy study. Patients appointed for colonoscopy will be invited to collect a faecal sample and mail it for analysis. The iFOBT result will be registered in a computer-based laboratory information system. The result of the colonoscopy will be registered in Danish national health registries. The sensitivity, specificity, positive predictive value and negative predictive value will be calculated as measures of the diagnostic properties of the iFOBT, using the result of colonoscopy as the reference standard. The accuracy of the test by type of alarm symptom will also be assessed.

Perspectives: The study will provide new and valuable data to evaluate the referral criteria for the cancer patient pathway. Given a good discriminatory ability of the iFOBT among symptomatic patients, fast-track colonoscopy may not be necessary as a first-choice examination in the diagnostic work-up of these patients.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Background: Colorectal cancer (CRC) is among the most frequent types of cancer in Denmark with 5,015 incident cases in 2015 (3,455 colon cancer and 1,560 rectal cancer), and an average annual number of deaths of 1900 persons in the period 2010-2014. Around 20% of patients are diagnosed in the most advanced stage of disease, contributing to high mortality, as an advanced stage of cancer is associated with a poor prognosis.

The Danish cancer patient pathway for CRC was implemented in 2008 with the aim of assuring fast and efficient diagnosing and treatment of cancer patients. In accordance with the cancer patient pathway, patients are referred by their general practitioner (GP) to fast-track colonoscopy when presenting with alarm symptoms such as rectal bleeding, change in bowel habits for more than four weeks, iron deficiency anaemia, and/or substantial general symptoms (e.g., weight loss or abdominal pain). Referral to colonoscopy is solely based on a clinical evaluation by the GP of the patient´s symptoms, still, the positive predictive value (PPV) of these criteria (i.e., the proportion of patients with alarm symptoms who have CRC) is only 3%-8%. At the same time, there is a considerable burden on endoscopy units to perform fast-track colonoscopies.

Immunochemical faecal occult blood tests (iFOBT) detect occult haemoglobin in the faeces, which may be caused by precancerous lesions or CRC. In the Danish national screening programme for CRC, the iFOBT employed is quantitative, and analysed by the OC-Sensor DIANA (Eiken Chemical Company, Ltd, Japan). Studies evaluating quantitative iFOBT to detect CRC in patients presenting with alarm symptoms, referred from primary care, report sensitivities ranging from 88% to 100%, specificities from 77% to 94%, PPV from 7% to 35%, and negative predictive values (NPV) from 98% to 100%. Overall, evidence of the accuracy of iFOBT in this population is limited and characterised by heterogeneous results, which is attributable to e.g., use of different cut-off values. Measuring faecal occult haemoglobin in patients with alarm symptoms may be a valuable tool for GPs deciding whether to refer the patient to fast-track colonoscopy. Not least, assessing the diagnostic accuracy of the iFOBT by type of alarm symptom and combinations of symptoms will provide insight into characteristics of patients that are likely to benefit from colonoscopy.

Aim: The aim of this study is to evaluate the diagnostic accuracy of the iFOBT among symptomatic patients who are referred to colonoscopy in the cancer patient pathway for CRC.

Materials and methods: The study will be conducted as a diagnostic accuracy study. Consecutive patients ≥40 years, referred to fast-track colonoscopy at the Regional Hospital of Horsens, will be invited by mail to collect a single faecal sample for haemoglobin measurement. The invitation will include a test kit with instructions, information about the study, and a consent form. Participants will be asked to collect the faecal sample before the laxative administration prior to colonoscopy, and immediately submit the sample for analysis at the Regional Hospital of Randers.

Faecal haemoglobin measurement will be conducted using the OC-Sensor DIANA analyser, and test results will be registered in the clinical laboratory information system. All participants will be examined by colonoscopy at the Regional Hospital of Horsens, and colonoscopy results will be registered in Danish national health registries. To obtain information on alarm symptoms, the patient´s GP will be asked to fill out a questionnaire concerning which type of alarm symptoms the patient presented with at the time of referral.

A positive iFOBT result (i.e., presence of occult blood in the faeces) will be defined as ≥35 µg haemoglobin/L. Patients will be considered to have been diagnosed with CRC by colonoscopy if they are registered by a relevant International Classification of Diseases, 10th edition (ICD-10) code for CRC, and a relevant procedure code for colonoscopy, and/or by a relevant Systematized Nomenclature of Medicine (SNOMED) code for CRC.

Using results of colonoscopy as the reference standard, the sensitivity, specificity, PPV, and NPV will be calculated as measures of the diagnostic accuracy of the iFOBT. The diagnostic accuracy of the iFOBT by sex, age, and type of alarm symptom will also be assessed.

Perspectives: This study will provide knowledge on the diagnostic value of the iFOBT among patients presenting with alarm symptoms of CRC in general practice. The study thus will contribute new and valuable data that may be used to evaluate the existing referral criteria for the cancer patient pathway.

Study Type

Interventional

Enrollment (Actual)

1258

Phase

  • Not Applicable

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

  • Denmark
      • Horsens, Denmark
        • Regionshospitalet Horsens

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

36 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Referred by a GP in the Central Denmark Region to colonoscopy in the cancer patient pathway for colorectal cancer.

Exclusion Criteria:

  • Referred to colonoscopy in the cancer patient pathway due to non-alarm symptoms.

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

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Immunochemical faecal occult blood test
All participants will collect a single faecal sample for haemoglobin measurement (immunochemical faecal occult blood test, iFOBT), and be examined by colonoscopy.
Diagnostic test: Immunochemical faecal occult blood test (iFOBT)
All participants in the study will collect a single faecal sample for haemoglobin measurement.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Faecal occult haemoglobin.
Time Frame: Through study completion, approximately 14 months
Numerical value of faecal occult haemoglobin concentration. Positive iFOBT results will be defined as ≥35 µg haemoglobin/L.
Through study completion, approximately 14 months
Colonic lesion.
Time Frame: Through study completion, approximately 14 months
Visualization of colonic lesions by colonoscopy.
Through study completion, approximately 14 months

Collaborators and Investigators

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

Sponsor

University of Aarhus

Collaborators

Central Denmark Region
Regionshospitalet Horsens
Randers Regional Hospital

Investigators

  • Principal Investigator: Cathrine Nielsen, PhD, University of Aarhus
  • Study Director: Peter Vedsted, Professor, University of Aarhus

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)

March 15, 2018

Primary Completion (Actual)

December 31, 2019

Study Completion (Actual)

December 31, 2019

Study Registration Dates

First Submitted

November 21, 2017

First Submitted That Met QC Criteria

December 8, 2017

First Posted (Actual)

December 11, 2017

Study Record Updates

Last Update Posted (Actual)

March 2, 2020

Last Update Submitted That Met QC Criteria

February 28, 2020

Last Verified

February 1, 2020

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 1234 (Department of Defense)

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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