Abstract

Simple SummaryPresently, constraints on colonoscopy capacity appear to be associated with inclusion of screening by direct colonoscopy or follow-up colonoscopy subsequent to a positive result of a feces-based screening concept. It is well known, however, that only a minority of the subjects with a positive feces test are diagnosed with bowel neoplasia at the subsequent follow-up colonoscopy. Therefore, a proposed Triage test concept, which includes (1) age of the subject; (2) concentration of occult blood in a feces test; (3) combinations of blood-based, cancer-associated biomarkers, may improve selection to follow-up colonoscopy in screening for bowel cancer. Thereby, the number of unnecessary colonoscopies may be reduced significantly, which may improve the national healthcare budgets, and indeed spare many subjects for the colonic examination, which is not free from adverse effects. Current research may identify and validate the optimal Triage screening concept.Implementation of population screening for colorectal cancer by direct colonoscopy or follow-up colonoscopy after a positive fecal blood test has challenged the overall capacity of bowel examinations. Certain countries are facing serious colonoscopy capacity constraints, which have led to waiting lists and long time latency of follow-up examinations. Various options for improvement are considered, including increased cut-off values of the fecal blood tests. Results from major clinical studies of blood-based, cancer-associated biomarkers have, however, led to focus on a Triage concept for improved selection to colonoscopy. The Triage test may include subject age, concentration of hemoglobin in a feces test and a combination of certain blood-based cancer-associated biomarkers. Recent results have indicated that Triage may reduce the requirements for colonoscopy by around 30%. Such results may be advantageous for the capacity, the healthcare budgets and in particular, the subjects, who do not need an unnecessary, unpleasant and risk-associated bowel examination.

Highlights

  • Many American citizens, uninsured with a positive FIT result, are far from instantly undergoing the recommended follow-up colonoscopy [13,14], and the lead-time has been shown to be associated with increased risk of CRC and higher stages at final diagnosis [15,16]

  • 20% of the subjects undergoing reduced. It is well-known that far from all colonoscopy procedures are needed; only some of adenoma control colonoscopy have new lesions [51] and only 25–30% of subjects undergoing the subjects with a positive FIT result have bowel lesions

  • Due Triage to present constraints with colonoscopy capacity in subject; relation to FIT-based level of hemoglobin in the FIT test; and (3) combined biomarkers, which may be a mix of proteins and screening, which has already been implemented or is under consideration for implementation, we ctDNA methylations, mutations and/or fragmentations (Figure 1) [23,24,25,26,27,28,29]

Read more

Summary

Introduction

Many American citizens, uninsured with a positive FIT result, are far from instantly undergoing the recommended follow-up colonoscopy [13,14], and the lead-time has been shown to be associated with increased risk of CRC and higher stages at final diagnosis [15,16]. Future achievements for improving CRC screening may consider combinations of FIT and blood-based biomarkers [39].

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call