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 inGut Vol. 58; no. 2; pp. 241 - 248
Main Authors Graser, A, Stieber, P, Nagel, D, Schäfer, C, Horst, D, Becker, C R, Nikolaou, K, Lottes, A, Geisbüsch, S, Kramer, H, Wagner, A C, Diepolder, H, Schirra, J, Roth, H J, Seidel, D, Göke, B, Reiser, M F, Kolligs, F T
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd and British Society of Gastroenterology 01.02.2009
BMJ Publishing Group
BMJ Publishing Group LTD
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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.
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
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  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
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  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
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  surname: Lottes
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  email: anno.graser@med.uni-muenchen.de
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  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
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  surname: Kramer
  fullname: Kramer, H
  email: anno.graser@med.uni-muenchen.de
  organization: Department of Clinical Radiology, University of Munich, Klinikum Grosshadern, Munich, Germany
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  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
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  surname: Diepolder
  fullname: Diepolder, H
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  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
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  surname: Roth
  fullname: Roth, H J
  email: anno.graser@med.uni-muenchen.de
  organization: Limbach Laboratory, Heidelberg, Germany
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  surname: Seidel
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  email: anno.graser@med.uni-muenchen.de
  organization: Department of Clinical Chemistry, University of Munich, Klinikum Grosshadern, Munich, Germany
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  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
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https://www.ncbi.nlm.nih.gov/pubmed/18852257$$D View this record in MEDLINE/PubMed
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Issue 2
Keywords Virtual colonoscopy
Sigmoidoscopy
Colonoscopy
Risk factor
Gastroenterology
Benign neoplasm
Adenoma
Colon
Endoscopy
Feces
Comparative study
Blood
Language English
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Snippet Background and aims:This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the...
Background and aims: This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the...
This prospective trial was designed to compare the performance characteristics of five different screening tests in parallel for the detection of advanced...
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StartPage 241
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
URI http://gut.bmj.com/content/58/2/241.full
https://api.istex.fr/ark:/67375/NVC-PJB0QBGK-9/fulltext.pdf
https://www.ncbi.nlm.nih.gov/pubmed/18852257
https://www.proquest.com/docview/1779344690
https://www.proquest.com/docview/66807753
Volume 58
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