Comparison of CT colonography, colonoscopy, sigmoidoscopy and faecal occult blood tests for the detection of advanced adenoma in an average risk population
Background and aims:This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the detection of advanced colonic neoplasia: CT colonography (CTC), colonoscopy (OC), flexible sigmoidoscopy (FS), faecal immunochemical stool testing...
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Published in | Gut Vol. 58; no. 2; pp. 241 - 248 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and British Society of Gastroenterology
01.02.2009
BMJ Publishing Group BMJ Publishing Group LTD |
Subjects | |
Online Access | Get full text |
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Abstract | Background and aims:This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the detection of advanced colonic neoplasia: CT colonography (CTC), colonoscopy (OC), flexible sigmoidoscopy (FS), faecal immunochemical stool testing (FIT) and faecal occult blood testing (FOBT).Methods:Average risk adults provided stool specimens for FOBT and FIT, and underwent same-day low-dose 64-multidetector row CTC and OC using segmentally unblinded OC as the standard of reference. Sensitivities and specificities were calculated for each single test, and for combinations of FS and stool tests. CTC radiation exposure was measured, and patient comfort levels and preferences were assessed by questionnaire.Results:221 adenomas were detected in 307 subjects who completed CTC (mean radiation dose, 4.5 mSv) and OC; 269 patients provided stool samples for both FOBT and FIT. Sensitivities of OC, CTC, FS, FIT and FOBT for advanced colonic neoplasia were 100% (95% CI 88.4% to 100%), 96.7% (82.8% to 99.9%), 83.3% (95% CI 65.3% to 94.4%), 32% (95% CI 14.9% to 53.5) and 20% (95% CI 6.8% to 40.7%), respectively. Combination of FS with FOBT or FIT led to no relevant increase in sensitivity. 12 of 45 advanced adenomas were smaller than 10 mm. 46% of patients preferred CTC and 37% preferred OC (p<0.001).Conclusions:High-resolution and low-dose CTC is feasible for colorectal cancer screening and reaches sensitivities comparable with OC for polyps >5 mm. For patients who refuse full bowel preparation and OC or CTC, FS should be preferred over stool tests. However, in cases where stool tests are performed, FIT should be recommended rather than FOBT. |
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AbstractList | This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the detection of advanced colonic neoplasia: CT colonography (CTC), colonoscopy (OC), flexible sigmoidoscopy (FS), faecal immunochemical stool testing (FIT) and faecal occult blood testing (FOBT).
Average risk adults provided stool specimens for FOBT and FIT, and underwent same-day low-dose 64-multidetector row CTC and OC using segmentally unblinded OC as the standard of reference. Sensitivities and specificities were calculated for each single test, and for combinations of FS and stool tests. CTC radiation exposure was measured, and patient comfort levels and preferences were assessed by questionnaire.
221 adenomas were detected in 307 subjects who completed CTC (mean radiation dose, 4.5 mSv) and OC; 269 patients provided stool samples for both FOBT and FIT. Sensitivities of OC, CTC, FS, FIT and FOBT for advanced colonic neoplasia were 100% (95% CI 88.4% to 100%), 96.7% (82.8% to 99.9%), 83.3% (95% CI 65.3% to 94.4%), 32% (95% CI 14.9% to 53.5) and 20% (95% CI 6.8% to 40.7%), respectively. Combination of FS with FOBT or FIT led to no relevant increase in sensitivity. 12 of 45 advanced adenomas were smaller than 10 mm. 46% of patients preferred CTC and 37% preferred OC (p<0.001).
High-resolution and low-dose CTC is feasible for colorectal cancer screening and reaches sensitivities comparable with OC for polyps >5 mm. For patients who refuse full bowel preparation and OC or CTC, FS should be preferred over stool tests. However, in cases where stool tests are performed, FIT should be recommended rather than FOBT. This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the detection of advanced colonic neoplasia: CT colonography (CTC), colonoscopy (OC), flexible sigmoidoscopy (FS), faecal immunochemical stool testing (FIT) and faecal occult blood testing (FOBT).BACKGROUND AND AIMSThis prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the detection of advanced colonic neoplasia: CT colonography (CTC), colonoscopy (OC), flexible sigmoidoscopy (FS), faecal immunochemical stool testing (FIT) and faecal occult blood testing (FOBT).Average risk adults provided stool specimens for FOBT and FIT, and underwent same-day low-dose 64-multidetector row CTC and OC using segmentally unblinded OC as the standard of reference. Sensitivities and specificities were calculated for each single test, and for combinations of FS and stool tests. CTC radiation exposure was measured, and patient comfort levels and preferences were assessed by questionnaire.METHODSAverage risk adults provided stool specimens for FOBT and FIT, and underwent same-day low-dose 64-multidetector row CTC and OC using segmentally unblinded OC as the standard of reference. Sensitivities and specificities were calculated for each single test, and for combinations of FS and stool tests. CTC radiation exposure was measured, and patient comfort levels and preferences were assessed by questionnaire.221 adenomas were detected in 307 subjects who completed CTC (mean radiation dose, 4.5 mSv) and OC; 269 patients provided stool samples for both FOBT and FIT. Sensitivities of OC, CTC, FS, FIT and FOBT for advanced colonic neoplasia were 100% (95% CI 88.4% to 100%), 96.7% (82.8% to 99.9%), 83.3% (95% CI 65.3% to 94.4%), 32% (95% CI 14.9% to 53.5) and 20% (95% CI 6.8% to 40.7%), respectively. Combination of FS with FOBT or FIT led to no relevant increase in sensitivity. 12 of 45 advanced adenomas were smaller than 10 mm. 46% of patients preferred CTC and 37% preferred OC (p<0.001).RESULTS221 adenomas were detected in 307 subjects who completed CTC (mean radiation dose, 4.5 mSv) and OC; 269 patients provided stool samples for both FOBT and FIT. Sensitivities of OC, CTC, FS, FIT and FOBT for advanced colonic neoplasia were 100% (95% CI 88.4% to 100%), 96.7% (82.8% to 99.9%), 83.3% (95% CI 65.3% to 94.4%), 32% (95% CI 14.9% to 53.5) and 20% (95% CI 6.8% to 40.7%), respectively. Combination of FS with FOBT or FIT led to no relevant increase in sensitivity. 12 of 45 advanced adenomas were smaller than 10 mm. 46% of patients preferred CTC and 37% preferred OC (p<0.001).High-resolution and low-dose CTC is feasible for colorectal cancer screening and reaches sensitivities comparable with OC for polyps >5 mm. For patients who refuse full bowel preparation and OC or CTC, FS should be preferred over stool tests. However, in cases where stool tests are performed, FIT should be recommended rather than FOBT.CONCLUSIONSHigh-resolution and low-dose CTC is feasible for colorectal cancer screening and reaches sensitivities comparable with OC for polyps >5 mm. For patients who refuse full bowel preparation and OC or CTC, FS should be preferred over stool tests. However, in cases where stool tests are performed, FIT should be recommended rather than FOBT. Background and aims: This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the detection of advanced colonic neoplasia: CT colonography (CTC), colonoscopy (OC), flexible sigmoidoscopy (FS), faecal immunochemical stool testing (FIT) and faecal occult blood testing (FOBT). Methods: Average risk adults provided stool specimens for FOBT and FIT, and underwent same-day low-dose 64-multidetector row CTC and OC using segmentally unblinded OC as the standard of reference. Sensitivities and specificities were calculated for each single test, and for combinations of FS and stool tests. CTC radiation exposure was measured, and patient comfort levels and preferences were assessed by questionnaire. Results: 221 adenomas were detected in 307 subjects who completed CTC (mean radiation dose, 4.5 mSv) and OC; 269 patients provided stool samples for both FOBT and FIT. Sensitivities of OC, CTC, FS, FIT and FOBT for advanced colonic neoplasia were 100% (95% CI 88.4% to 100%), 96.7% (82.8% to 99.9%), 83.3% (95% CI 65.3% to 94.4%), 32% (95% CI 14.9% to 53.5) and 20% (95% CI 6.8% to 40.7%), respectively. Combination of FS with FOBT or FIT led to no relevant increase in sensitivity. 12 of 45 advanced adenomas were smaller than 10 mm. 46% of patients preferred CTC and 37% preferred OC (p<0.001). Conclusions: High-resolution and low-dose CTC is feasible for colorectal cancer screening and reaches sensitivities comparable with OC for polyps >5 mm. For patients who refuse full bowel preparation and OC or CTC, FS should be preferred over stool tests. However, in cases where stool tests are performed, FIT should be recommended rather than FOBT. |
Author | Lottes, A Diepolder, H Kramer, H Seidel, D Nagel, D Stieber, P Schirra, J Kolligs, F T Göke, B Becker, C R Schäfer, C Reiser, M F Roth, H J Geisbüsch, S Graser, A Wagner, A C Horst, D Nikolaou, K |
Author_xml | – sequence: 1 givenname: A surname: Graser fullname: Graser, A email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Radiology, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 2 givenname: P surname: Stieber fullname: Stieber, P email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Chemistry, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 3 givenname: D surname: Nagel fullname: Nagel, D email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Chemistry, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 4 givenname: C surname: Schäfer fullname: Schäfer, C email: anno.graser@med.uni-muenchen.de organization: Department of Medicine II, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 5 givenname: D surname: Horst fullname: Horst, D email: anno.graser@med.uni-muenchen.de organization: Department of Pathology, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 6 givenname: C R surname: Becker fullname: Becker, C R email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Radiology, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 7 givenname: K surname: Nikolaou fullname: Nikolaou, K email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Radiology, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 8 givenname: A surname: Lottes fullname: Lottes, A email: anno.graser@med.uni-muenchen.de organization: Department of Medicine II, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 9 givenname: S surname: Geisbüsch fullname: Geisbüsch, S email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Radiology, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 10 givenname: H surname: Kramer fullname: Kramer, H email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Radiology, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 11 givenname: A C surname: Wagner fullname: Wagner, A C email: anno.graser@med.uni-muenchen.de organization: Department of Medicine II, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 12 givenname: H surname: Diepolder fullname: Diepolder, H email: anno.graser@med.uni-muenchen.de organization: Department of Medicine II, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 13 givenname: J surname: Schirra fullname: Schirra, J email: anno.graser@med.uni-muenchen.de organization: Department of Medicine II, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 14 givenname: H J surname: Roth fullname: Roth, H J email: anno.graser@med.uni-muenchen.de organization: Limbach Laboratory, Heidelberg, Germany – sequence: 15 givenname: D surname: Seidel fullname: Seidel, D email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Chemistry, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 16 givenname: B surname: Göke fullname: Göke, B email: anno.graser@med.uni-muenchen.de organization: Department of Medicine II, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 17 givenname: M F surname: Reiser fullname: Reiser, M F email: anno.graser@med.uni-muenchen.de organization: Department of Clinical Radiology, University of Munich, Klinikum Grosshadern, Munich, Germany – sequence: 18 givenname: F T surname: Kolligs fullname: Kolligs, F T email: anno.graser@med.uni-muenchen.de organization: Department of Medicine II, University of Munich, Klinikum Grosshadern, Munich, Germany |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20992874$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/18852257$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Adenoma - diagnosis Aged Aged, 80 and over Biological and medical sciences Colon - pathology Colonic Polyps - diagnosis Colonography, Computed Tomographic - methods Colonoscopy Colonoscopy - methods Colorectal cancer Colorectal Neoplasms - diagnosis Contrast agents Digestive system Digestive system. Abdomen Drug dosages Endoscopy Feces - chemistry Female Gastroenterology. Liver. Pancreas. Abdomen Hemoglobins - analysis Humans Imaging, Three-Dimensional Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Medical screening Middle Aged Occult Blood Patients Polyethylene glycol Polyps Prospective Studies Radiation Radiodiagnosis. Nmr imagery. Nmr spectrometry Rectum - pathology Sample Size Scanners Sensitivity and Specificity Sigmoidoscopy - methods Tumors |
Title | Comparison of CT colonography, colonoscopy, sigmoidoscopy and faecal occult blood tests for the detection of advanced adenoma in an average risk population |
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