Abstract

BackgroundThe aim was to improve upon an existing blood-based colorectal cancer (CRC) test directed to high-risk symptomatic patients, by developing a new CRC classifier to be used with a new test embodiment. The new test uses a robust assay format—electrochemiluminescence immunoassays—to quantify protein concentrations. The aim was achieved by building and validating a CRC classifier using concentration measures from a large sample set representing a true intent-to-test (ITT) symptomatic population.Methods4435 patient samples were drawn from the Endoscopy II sample set. Samples were collected at seven hospitals across Denmark between 2010 and 2012 from subjects with symptoms of colorectal neoplasia. Colonoscopies revealed the presence or absence of CRC. 27 blood plasma proteins were selected as candidate biomarkers based on previous studies. Multiplexed electrochemiluminescence assays were used to measure the concentrations of these 27 proteins in all 4435 samples. 3066 patients were randomly assigned to the Discovery set, in which machine learning was used to build candidate classifiers. Some classifiers were refined by allowing up to a 25% indeterminate score range. The classifier with the best Discovery set performance was successfully validated in the separate Validation set, consisting of 1336 samples.ResultsThe final classifier was a logistic regression using ten predictors: eight proteins (A1AG, CEA, CO9, DPPIV, MIF, PKM2, SAA, TFRC), age, and gender. In validation, the indeterminate rate of the new panel was 23.2%, sensitivity/specificity was 0.80/0.83, PPV was 36.5%, and NPV was 97.1%.ConclusionsThe validated classifier serves as the basis of a new blood-based CRC test for symptomatic patients. The improved performance, resulting from robust concentration measures across a large sample set mirroring the ITT population, renders the new test the best available for this population. Results from a test using this classifier can help assess symptomatic patients’ CRC risk, increase their colonoscopy compliance, and manage next steps in their care.

Highlights

  • The aim was to improve upon an existing blood-based colorectal cancer (CRC) test directed to highrisk symptomatic patients, by developing a new CRC classifier to be used with a new test embodiment

  • By focusing on CRC risk stratification within symptomatic patients, the expectation is that the colonoscopy compliance of patients with the apparent highest need can be increased

  • Our view is that CRC tests for symptomatic patients are most helpful when directed to patients who resist colonoscopies despite the presence of symptoms

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Summary

Introduction

The aim was to improve upon an existing blood-based colorectal cancer (CRC) test directed to highrisk symptomatic patients, by developing a new CRC classifier to be used with a new test embodiment. A low-burden CRC screening test, such as a bloodbased test, has been widely sought. It has proven difficult to find blood-based CRC signal with performance matching that of colonoscopy or of stool-based tests across average risk patients. The increased CRC prevalence in the symptomatic population (10.9% in a Danish symptomatic cohort [10], as compared to 0.5–0.7% in the average risk population [7, 9]) would seem sufficient incentive for patients to follow clinicians’ recommendations to have colonoscopies. A low-burden CRC test for this population would highlight patient risk stratification, resulting in increased personalized incentive and increased colonoscopy compliance [11, 12]

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