Skip to main content
Erschienen in: BMC Medical Imaging 1/2020

Open Access 01.12.2020 | Research article

Computed tomography colonography versus colonoscopy for detection of colorectal cancer: a diagnostic performance study

verfasst von: Junping sha, Jun chen, Xuguang lv, Shaoxin liu, Ruihong chen, Zhibing zhang

Erschienen in: BMC Medical Imaging | Ausgabe 1/2020

Abstract

Background

Colonoscopy is the reference standard for the detection of colorectal cancer but it is an invasive technique and has the risk of bowel perforation and bleeding. Unlike colonoscopy, sedation is not required in computed tomography colonography and requires additional reassurance endoscopy. The objectives of the study were to compare the diagnostic performance of computed tomography colonography against colonoscopy for a diagnosis of colorectal cancer.

Methods

Data regarding any polyp ≥10 mm diameter (ø) and < 10 mm ø but suspicious polyps of computed tomography colonography (n = 318), colonoscopy (n = 318), and surgical pathology (n = 77) for symptomatic colorectal cancer patients were collected and analyzed. Lesion ulceration, extramural invasion, and/ or lesion shouldering was considered as a suspicious polyp. Beneficial scores for decision making of curative surgeries were evaluated for each modality. The cost of diagnosis of colorectal cancer was also evaluated.

Results

Either of diagnosis showed polyps ≥10 mm ø in 27 patients and polyps of 50 patients were < 10 mm ø but suspicious. Therefore, a total of 77 patients were subjected to surgery. With respect to surgical pathology, sensitivities for computed tomographic colonography and colonoscopy were 0.961 and 0.831. For detection of ≥10 mm ø polyp, benefit score for computed tomographic colonography and colonoscopy were 0–0.906 diagnostic confidence and 0.035–0.5 diagnostic confidence. For polyps, ≥ 10 mm ø but not too many large polyps, colonoscopy had the risk of underdiagnosis. For < 10 mm ø but suspicious polyps, < 0.6 mm ø and < 2.2 mm ⌀ polyps could not be detected by computed tomographic colonography and colonoscopy, respectively. The computed tomographic colonography had less cost than colonoscopy (1345 ± 135 ¥/ patient vs. 1715 ± 241 ¥/ patient, p < 0.0001) for diagnosis of colorectal cancer.

Conclusion

Computed tomographic colonography would be a non-inferior alternative than colonoscopy for a diagnosis of colorectal cancer.

Level of evidence

III.
Hinweise

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
STROBE
Strengthening the reporting of observational studies in epidemiology
Diameter

Background

Colorectal cancer is the fourth most common cancer in China [1]. High red and processed meat intake in the Chinese population is responsible for colorectal cancer [2]. Several methods are available for the diagnosis of colorectal cancer but it is usually made by colonoscopy [3]. Colonoscopy is the reference standard for the detection of colorectal cancer [4] but it is an invasive technique and has the risk of bowel perforation and bleeding [5]. Sedation is also required which increases the risk especially in old aged patients [6]. Sedation is not required in computed tomography colonography [7]. Computed tomography colonography has a high sensitivity for large polyps in asymptomatic [8] and symptomatic [9] population but it images outside the organ [10], requires additional reassurance endoscopy to biopsy lead to increases the cost and burden of the diagnosis [11], and requires quality assurance for radiologists [12]. However, the study suggested that computed tomography colonography has the same sensitivity to colonoscopy for the detection of colorectal cancer [4] but has an issue of the small effect and the large variability in the study which may have type-II errors [13]. Large benign colorectal precursor mass lesions of invasive malignant cancers present challenges in both computed tomography colonography and colonoscopy [8]. In short, detection of colorectal cancer is critical irrespective of symptoms and age.
The objectives of the retrospective study were to compare diagnostic performance, cost, and safety of computed tomography colonography against colonoscopy for the diagnosis of colorectal cancer considering surgical pathology as a reference standard in symptomatic patients.

Methods

Study population

From 15 January 2019 to 1 November 2019, a total of 326 patients were available at the department of gastroenterology of the Xiantao First People’s Hospital Affiliated to Yangtze University, Xiantao, Hubei, China and the Renmin Hospital of Wuhan University, Wuhan, Hubei, China who had symptom(s) suggestive of colorectal cancer such as abdominal pain, rectal bleeding, and/ or change in bowel habits, need whole-colon examinations, and performed both computed tomography colonography and colonoscopy. Among them, five patients have known diagnosis of ulcerative colitis and three patients were undergone whole-colon examinations in the last 6-months. Therefore, the data of these patients were not included in the analyses and data of 318 symptomatic patients suggestive of colorectal cancer were included in the analysis (Fig. 1).

Computed tomographic colonography

All patients have injected 20 mg intravenous hyoscine (Buscopan, Sanofi, Berkshire, UK) before the examination. Intravenous contrast was administered on demand and computed tomographic colonography was performed as per international guidelines for good clinical practice under a single breath-hold of the patient using a multidetector instrument (GE Healthcare, New York, USA). Patients were scanned both supine and prone positions by radiologists (minimum of 3-years of experience in abdominal imaging) of institutes. Images acquired using 0.125 cm collimation, 0.1 cm reconstruction interval, 119 kVp, and 51–74 mAs fixed tube current-time product or 28–290 mA tube current modulation. The examinations involved identification of colorectal neoplasia (any polyp 10 mm or more in diameter (ø) and polyps less than 10 mm ø but suspicious).

Colonoscopy

It was performed using video endoscopes (RetroView™ Colonoscopes EC34-i10T, PENTAX Medical, New Jersey, USA) after bowel preparation under midazolam/ fentanyl sedation. Gastroenterologists or colorectal surgeons (minimum of 3-years of experience) of institutes performed the colonoscopy. The examinations were performed as per the institutional protocol and detected lesions were evaluated by biopsies (performed by pathologists, a minimum 3-years of experience of institutes).

Image analysis

Colonoscopy performed after computed tomographic colonography. Lesion ulceration (Fig. 2), extramural invasion (Fig. 3), and/ or lesion shouldering (Fig. 4) was considered as a suspicious polyp (as directed by the internal-institutional guideline for colorectal cancer). Image analyses performed by radiologists (minimum of 7-years of experience in abdominal imaging) of institutes.

Surgery

Patients who had polyp 10 mm ø or more and polyps less than 10 mm ø but suspicious in either of modality were subjected to endoscopy (performed by endoscopists, a minimum 3-years of experience of institutes) following biopsies (performed by pathologists, a minimum 3-years of experience of institutes). Histologically (performed by pathologists, a minimum 3-years of experience of institutes, after the computed tomographic colonography and colonoscopy) confirmed suspicious polyps and 10 mm ø or more polyps (due to symptoms) were removed by colorectal surgeons (minimum of 3-years of experience) of institutes.

Benefit score analysis

Benefit score analysis for each diagnosis modality for detection of 10 mm and more ø polyps was calculated as per Eq. 1 and that for less than 10 mm ø but suspicious polyps were calculated a were calculated as per Eq. 2 [14]:
$$ \mathrm{Benefit}\ \mathrm{score}=\frac{\mathrm{True}\ \mathrm{positive}\ge 10\ \mathrm{mm}\o \mathrm{polyp}}{\mathrm{Total}\ \mathrm{numbers}\ \mathrm{of}\ \mathrm{patients}\ \mathrm{diagnosed}}-\left(\frac{\mathrm{False}-\mathrm{positive}\ge 10\ \mathrm{mm}\o \mathrm{polyp}}{\mathrm{Total}\ \mathrm{numbers}\ \mathrm{of}\ \mathrm{patients}\ \mathrm{diagnosed}}\times \frac{\mathrm{Level}\ \mathrm{of}\ \mathrm{diagnostic}\ \mathrm{confidence}\ \mathrm{above}\ \mathrm{which}\ \mathrm{decision}\ \mathrm{of}\ \mathrm{surgery}\ \mathrm{was}\ \mathrm{taken}}{1-\mathrm{Level}\ \mathrm{of}\ \mathrm{diagnostic}\ \mathrm{confidence}\ \mathrm{above}\ \mathrm{which}\ \mathrm{decision}\ \mathrm{of}\ \mathrm{surgery}\ \mathrm{was}\ \mathrm{taken}}\right) $$
(1)
$$ \mathrm{Benefit}\ \mathrm{score}=\frac{\mathrm{True}\ \mathrm{positive}<10\ \mathrm{mm}\o \mathrm{but}\ \mathrm{the}\ \mathrm{suspicious}\ \mathrm{polyp}}{\mathrm{Total}\ \mathrm{numbers}\ \mathrm{of}\ \mathrm{patients}\ \mathrm{diagnosed}}-\left(\frac{\mathrm{False}-\mathrm{positive}<10\ \mathrm{mm}\o \mathrm{but}\ \mathrm{the}\ \mathrm{suspicious}\ \mathrm{polyp}}{\mathrm{Total}\ \mathrm{numbers}\ \mathrm{of}\ \mathrm{patients}\ \mathrm{diagnosed}}\times \frac{\mathrm{Level}\ \mathrm{of}\ \mathrm{diagnostic}\ \mathrm{confidence}\ \mathrm{above}\ \mathrm{which}\ \mathrm{decision}\ \mathrm{of}\ \mathrm{surgery}\ \mathrm{was}\ \mathrm{taken}}{1-\mathrm{Level}\ \mathrm{of}\ \mathrm{diagnostic}\ \mathrm{confidence}\ \mathrm{above}\ \mathrm{which}\ \mathrm{decision}\ \mathrm{of}\ \mathrm{surgery}\ \mathrm{was}\ \mathrm{taken}}\right) $$
(2)

Cost

The cost of diagnosis of colorectal cancer with computed tomographic colonography (is not of diagnostic colonography and colonoscopy to confirm the positive result of computed tomographic colonography prior to surgery) and colonography was calculated.

Adverse events

Any reported adverse effects after diagnosis procedures including hospitalization were noted.

Statistical analysis

InStat, GraphPad, San Diego, CA, USA was used for statistical analyses. The sample size was calculated at 80% of power and a 5% level of confidence. The Fischer exact test was performed for categorical data [4]. Mann-Whitney U-test was used for continuous data [3]. The results were considered significant at a 95% level of confidence.

Results

Demographic parameters

The average age of patients was 65.12 ± 7.28 years and 183 (58%) patients were women. The enrolled patients had symptoms like abdominal pain, rectal bleeding, and/ or change in bowel habits. Patients reported one or more than one symptom suggestive of colorectal cancer and needed whole-colon examinations (Table 1). All patients had performed radiological diagnosis within 2-weeks after recommendation by the respective consultant(s).
Table 1
Demographic parameters and clinical conditions of diagnosed patients
Parameters
Value
Patients
318
Age (years)
Minimum
30
Maximum
75
Mean ± SD
65.12 ± 7.28
Gender
Male
135(42)
Female
183(58)
Ethnicity
Han Chinese
292(92)
Mongolian
23(7)
Tibetan
3(1)
Symptoms
Abdominal pain
201(63)
Rectal bleeding
53(17)
Change in bowel habit
278(87)
Anemia
171(54)
Weight loss
151(48)
Route of referral
Gastroenterology
205(64)
Colorectal surgical clinic
85(27)
Geriatrics
28(9)
Continuous data are presented as mean ± SD and categorical data are presented as frequency (percentage)

Diagnostic performance

Either diagnosis showed polyps 10 mm ø and more in 27 patients and polyps of 50 patients were less than 10 mm ø but suspicious. Therefore, a total of 77 patients were subjected to surgery and surgical pathology (Table 2).
Table 2
Performance of diagnostic methods
Parameters
Surgical pathology
Computed tomographic colonography
Colonoscopy
Patients
77
318
*p-value
318
*p-value
Polyp ≥10 mm ø
25(32)
27(8)
0.863
23(7)
0.859
Polyps < 10 mm ø but suspicious
49(64)
47(15)
41(13)
Non suspicious and < 10 mm ø polyps
3(4)
239(75) **
< 0.0001
247(78)**
< 0.0001
Inconclusive results
0(0)
5(2)
0.588
7(2)
0.354
Data are presented as frequency (percentage)
*Respect to surgical pathology
Lesion ulceration, extramural invasion, and/ or lesion shouldering was considered as suspicious polyp
The Fischer exact test was used statistical analysis
A p < 0.05 was considered significant
**Significant difference with respect to surgical pathology
ø: Diameter
With respect to surgical pathology, sensitivities for computed tomographic colonography and colonoscopy were 0.961 and 0.831 and accuracies were reported in Table 3.
Table 3
Accuracies of diagnostic methods
Parameters
Computed tomographic colonography
Colonoscopy
For polyp ≥10 mm ø
0.926
0.920
For polyps < 10 mm ø but suspicious
0.959
0.837
Lesion ulceration, extramural invasion, and/ or lesion shouldering was considered as suspicious polyp
ø: Diameter

Benefit score analysis

For detection of 10 mm ø or more polyp, benefit score for computed tomographic colonography and colonoscopy were 0–0.906 diagnostic confidence and 0.035–0.5 diagnostic confidence. For polyps 10 mm ø or more but not too many large polyps, colonoscopy had a risk of underdiagnosis (Fig. 5). For less than 10 mm ø but suspicious polyps, computed tomographic colonography could detect 0.6–9.99 mm ø polyps while colonoscopy could detect 2.2–9.99 mm ø polyps. Less than 0.6 mm ø and less than 2.2 mm ø suspicious polyps could not be detected by computed tomographic colonography and colonoscopy, respectively (Fig. 6).

Cost

The computed tomographic colonography had less cost than colonoscopy (1345 ± 135 ¥/ patient vs. 1715 ± 241 ¥/ patient, p < 0.0001) for diagnosis of colorectal cancer (Fig. 7).

Adverse events

An unplanned hospital admission within a month occurred in two patients due to bowel perforation. No death was reported within 3-months after diagnosis.

Discussion

The computed tomographic colonography had high sensitivity for colorectal polyps, high accuracy for polyps ≥10 mm ø and polyps < 10 mm ø but suspicious polyps, and less cost than colonoscopy. The results of the study were consistent with the SIGGAR trial [3, 4]. The computed tomographic colonography would be an alternative method than colonoscopy for detection of colorectal cancer.
The study reported that colonoscopy had underdiagnosis and computed tomographic colonography had overdiagnosis for polyps ≥10 mm ø. The results of the study were in line with the SIGGAR trial [3, 5, 15]. The different morphological characteristics of lesions and inadequate bowel preparation reduce the sensitivity of colonoscopy [16]. Extracolonic abnormalities detected by computed tomographic colonography would lead to overdiagnosis of colorectal cancer [17]. Endoscopy and contrast agents may overcome the overdiagnosis of computed tomographic colonography.
The cut-off for suspicious polyps for computed tomographic colonography was 0.6 mm ø and that for colonoscopy was 2.2 mm ø. The results of the study agreed with the statement of the second ESGAR consensus [18]. The use of endoscopy and contrast agents with computed tomographic colonography and inadequate bowel preparation were responsible for these results [4]. Evidence-based guidelines are needed for the threshold value of suspicious polyps in colorectal cancer.
Computed tomographic colonography was cost-effective than colonoscopy for a diagnosis of colorectal cancer. The results of the study were consistent with the SIGGAR trial [3] and a randomized controlled trial [19]. Biopsies and cytopathology would lead to an increase in the cost of colonoscopy [20]. The cost for diagnosis of colorectal polyps in follow-up after curative surgery is also required to consider to reach any conclusion.
Two patients reported bowel perforation and hospitalization after diagnosis. Colonoscopy is responsible for the perforation of the bowel and unplanned hospitalization [5]. The results of the study were consistent with the SIGGAR trial [3]. Computed tomographic colonography would be safe than colonoscopy.
Several limitations of the study reported, for example, retrospective reviews and lack of randomized trial but in diagnostic performance study, randomized trials are difficult to design. The extracolonic abnormalities detected by computed tomographic colonography did not report and discuss. The methods adopted for diagnosis after curative surgeries and costs for the same were not reported. In the long-term, follow-up acceptability and psychologic consequences of patients for colonoscopy are higher than the computed tomographic colonography [15] because of lifetime burden of the computed tomographic colonography [11] but data regarding acceptability, psychologic consequences, and inter-and interobserver’ agreements of the diagnosis methods did not discuss.

Conclusions

Computed tomographic colonography had high sensitivity, high accuracy (for polyps ≥10 mm in diameter and polyps < 10 mm in diameter but suspicious polyps), less cost, and safe than colonoscopy for a diagnosis of colorectal cancer in symptomatic patients. Computed tomographic colonography had 0.6 mm in diameter and colonoscopy had a 2.2 mm in diameter threshold for suspicious polyps. Computed tomographic colonography would be a non-inferior alternative than colonoscopy for the diagnosis of colorectal cancer. A large randomized trial is required including postoperative follow-up data for diagnosis of colorectal cancer to state hypothesis clearly. The results of the current study help to the health services regarding the detection of colorectal cancer for Medicare beneficiaries.

Acknowledgments

Authors are thankful for the medical and radiological staff of the Xiantao First People’s Hospital Affiliated to Yangtze University, Xiantao, Hubei, China and the Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
The designed protocol (XAY/CL/14/19 dated 10 December 2019) of the established study was approved by the Yangtze University and the Wuhan University review boards. The study reporting adheres to the law of China, strengthening the reporting of observational studies in epidemiology (STROBE) statement: Cross-sectional study, and the V2008 of Helsinki Declarations. An informed consent form was signed by all participating patients regarding diagnosis, endoscopy, and surgery (if required) during hospitalization.
An informed consent form was signed by all participating patients regarding the publication of the study including personal data during hospitalization.

Competing interests

The authors declared that they have no conflict of interest or any other competing interest regarding results and/or discussion reported in the research.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Literatur
1.
Zurück zum Zitat Gu MJ, Huang QC, Bao CZ, Li YJ, Li XQ, Ye D, Ye ZH, Chen K, Wang JB. Attributable causes of colorectal cancer in China. BMC Cancer. 2018;18:38.CrossRef Gu MJ, Huang QC, Bao CZ, Li YJ, Li XQ, Ye D, Ye ZH, Chen K, Wang JB. Attributable causes of colorectal cancer in China. BMC Cancer. 2018;18:38.CrossRef
2.
Zurück zum Zitat Bernstein AM, Song M, Zhang X, Pan A, Wang M, Fuchs CS, Le N, Chan AT, Willett WC, Ogino S, Giovannucci EL, Wu K. Processed and unprocessed red meat and risk of colorectal cancer: analysis by tumor location and modification by time. PLoS One. 2015;10:e0135959.CrossRef Bernstein AM, Song M, Zhang X, Pan A, Wang M, Fuchs CS, Le N, Chan AT, Willett WC, Ogino S, Giovannucci EL, Wu K. Processed and unprocessed red meat and risk of colorectal cancer: analysis by tumor location and modification by time. PLoS One. 2015;10:e0135959.CrossRef
3.
Zurück zum Zitat Halligan S, Dadswell E, Wooldrage K, Wardle J, von Wagner C, Lilford R, Yao GL, Zhu S, Atkin W. Computed tomographic colonography compared with colonoscopy or barium enema for diagnosis of colorectal cancer in older symptomatic patients: two multicentre randomised trials with economic evaluation (the SIGGAR trials). Health Technol Assess. 2015;19:1–134.CrossRef Halligan S, Dadswell E, Wooldrage K, Wardle J, von Wagner C, Lilford R, Yao GL, Zhu S, Atkin W. Computed tomographic colonography compared with colonoscopy or barium enema for diagnosis of colorectal cancer in older symptomatic patients: two multicentre randomised trials with economic evaluation (the SIGGAR trials). Health Technol Assess. 2015;19:1–134.CrossRef
4.
Zurück zum Zitat Atkin W, Dadswell E, Wooldrage K, Kralj-Hans I, von Wagner C, Edwards R, Yao G, Kay C, Burling D, Faiz O, Teare J, Lilford RJ, Morton D, Wardle J, Halligan S, SIGGAR investigators. Computed tomographic colonography versus colonoscopy for investigation of patients with symptoms suggestive of colorectal cancer (SIGGAR): a multicentre randomised trial. Lancet. 2013;381:1194–202.CrossRef Atkin W, Dadswell E, Wooldrage K, Kralj-Hans I, von Wagner C, Edwards R, Yao G, Kay C, Burling D, Faiz O, Teare J, Lilford RJ, Morton D, Wardle J, Halligan S, SIGGAR investigators. Computed tomographic colonography versus colonoscopy for investigation of patients with symptoms suggestive of colorectal cancer (SIGGAR): a multicentre randomised trial. Lancet. 2013;381:1194–202.CrossRef
5.
Zurück zum Zitat Wang L, Mannalithara A, Singh G, Ladabaum U. Low rates of gastrointestinal and non-gastrointestinal complications for screening or surveillance colonoscopies in a population-based study. Gastroenterology. 2018;154:540–55.CrossRef Wang L, Mannalithara A, Singh G, Ladabaum U. Low rates of gastrointestinal and non-gastrointestinal complications for screening or surveillance colonoscopies in a population-based study. Gastroenterology. 2018;154:540–55.CrossRef
6.
Zurück zum Zitat Lovett P, Gomez V, Hodge DO, Ladlie B. Propofol versus midazolam/fentanyl sedation for colonoscopy in the elderly patient population. J Perianesth Nurs. 2017;32:210–4.CrossRef Lovett P, Gomez V, Hodge DO, Ladlie B. Propofol versus midazolam/fentanyl sedation for colonoscopy in the elderly patient population. J Perianesth Nurs. 2017;32:210–4.CrossRef
7.
Zurück zum Zitat Meiklejohn DJ, Ridley LJ, Ngu MC, Cowlishaw JL, Duller A, Ridley W. Utility of minimal preparation computed tomography colonography in detecting colorectal cancer in elderly and frail patients. Intern Med J. 2018;48:1492–8.CrossRef Meiklejohn DJ, Ridley LJ, Ngu MC, Cowlishaw JL, Duller A, Ridley W. Utility of minimal preparation computed tomography colonography in detecting colorectal cancer in elderly and frail patients. Intern Med J. 2018;48:1492–8.CrossRef
8.
Zurück zum Zitat Pooler BD, Lubner MG, Theis JR, Halberg RB, Liang Z, Pickhardt PJ. Volumetric textural analysis of colorectal masses at CT colonography: differentiating benign versus malignant pathology and comparison with human reader performance. Acad Radiol. 2019;26:30–7.CrossRef Pooler BD, Lubner MG, Theis JR, Halberg RB, Liang Z, Pickhardt PJ. Volumetric textural analysis of colorectal masses at CT colonography: differentiating benign versus malignant pathology and comparison with human reader performance. Acad Radiol. 2019;26:30–7.CrossRef
9.
Zurück zum Zitat Pickhardt PJ, Correale L, Delsanto S, Regge D, Hassan C. CT colonography performance for the detection of polyps and cancer in adults ≥ 65 years old: systematic review and meta-analysis. Am J Roentgenol. 2018;211:40–51.CrossRef Pickhardt PJ, Correale L, Delsanto S, Regge D, Hassan C. CT colonography performance for the detection of polyps and cancer in adults ≥ 65 years old: systematic review and meta-analysis. Am J Roentgenol. 2018;211:40–51.CrossRef
10.
Zurück zum Zitat Yee J, McFarland E. Extracolonic findings and radiation at CT colonography: what the referring provider needs to know. Abdom Radiol. 2018;43:554–65.CrossRef Yee J, McFarland E. Extracolonic findings and radiation at CT colonography: what the referring provider needs to know. Abdom Radiol. 2018;43:554–65.CrossRef
11.
Zurück zum Zitat Knudsen AB, Zauber AG, Rutter CM, Naber SK, Doria-Rose VP, Pabiniak C, Johanson C, Fischer SE, Lansdorp-Vogelaar I, Kuntz KM. Estimation of benefits, burden, and harms of colorectal cancer screening strategies: modeling study for the us preventive services task force. JAMA. 2016;315:2595–609.CrossRef Knudsen AB, Zauber AG, Rutter CM, Naber SK, Doria-Rose VP, Pabiniak C, Johanson C, Fischer SE, Lansdorp-Vogelaar I, Kuntz KM. Estimation of benefits, burden, and harms of colorectal cancer screening strategies: modeling study for the us preventive services task force. JAMA. 2016;315:2595–609.CrossRef
12.
Zurück zum Zitat Halligan S, Wooldrage K, Dadswell E, Kralj-Hans I, von Wagner C, Edwards R, Yao G, Kay C, Burling D, Faiz O, Teare J, Lilford RJ, Morton D, Wardle J, Atkin W, SIGGAR investigators. Computed tomographic colonography versus barium enema for diagnosis of colorectal cancer or large polyps in symptomatic patients (SIGGAR): a multicentre randomised trial. Lancet. 2013;381:1185–93.CrossRef Halligan S, Wooldrage K, Dadswell E, Kralj-Hans I, von Wagner C, Edwards R, Yao G, Kay C, Burling D, Faiz O, Teare J, Lilford RJ, Morton D, Wardle J, Atkin W, SIGGAR investigators. Computed tomographic colonography versus barium enema for diagnosis of colorectal cancer or large polyps in symptomatic patients (SIGGAR): a multicentre randomised trial. Lancet. 2013;381:1185–93.CrossRef
13.
Zurück zum Zitat Columb MO, Atkinson MS. Statistical analysis: sample size and power estimations. BJA Educ. 2015;16:159–61.CrossRef Columb MO, Atkinson MS. Statistical analysis: sample size and power estimations. BJA Educ. 2015;16:159–61.CrossRef
14.
Zurück zum Zitat Li J, Yu Y, Zhu L, Li Y, He Q. Magnetic resonance imaging versus computed tomography for biliary tract intraductal papillary mucinous neoplasm (BT-IPMN): A diagnostic performance analysis. Med Sci Monit. 2020;26:e920952 1–9.PubMedPubMedCentral Li J, Yu Y, Zhu L, Li Y, He Q. Magnetic resonance imaging versus computed tomography for biliary tract intraductal papillary mucinous neoplasm (BT-IPMN): A diagnostic performance analysis. Med Sci Monit. 2020;26:e920952 1–9.PubMedPubMedCentral
15.
Zurück zum Zitat von Wagner C, Ghanouni A, Halligan S, Smith S, Dadswell E, Lilford RJ, Morton D, Atkin W, Wardle J, Investigators SIGGAR. Patient acceptability and psychologic consequences of CT colonography compared with those of colonoscopy: results from a multicenter randomized controlled trial of symptomatic patients. Radiology. 2012;263:723–31.CrossRef von Wagner C, Ghanouni A, Halligan S, Smith S, Dadswell E, Lilford RJ, Morton D, Atkin W, Wardle J, Investigators SIGGAR. Patient acceptability and psychologic consequences of CT colonography compared with those of colonoscopy: results from a multicenter randomized controlled trial of symptomatic patients. Radiology. 2012;263:723–31.CrossRef
16.
17.
Zurück zum Zitat Halligan S, Wooldrage K, Dadswell E, Shah U, Kralj-Hans I, von Wagner C, Faiz O, Teare J, Edwards R, Kay C, Yao G, Lilford RJ, Morton D, Wardle J, Atkin W, Investigators SIGGAR. Identification of extracolonic pathologies by computed tomographic colonography in colorectal cancer symptomatic patients. Gastroenterology. 2015;149:89–101.CrossRef Halligan S, Wooldrage K, Dadswell E, Shah U, Kralj-Hans I, von Wagner C, Faiz O, Teare J, Edwards R, Kay C, Yao G, Lilford RJ, Morton D, Wardle J, Atkin W, Investigators SIGGAR. Identification of extracolonic pathologies by computed tomographic colonography in colorectal cancer symptomatic patients. Gastroenterology. 2015;149:89–101.CrossRef
18.
Zurück zum Zitat Neri E, Halligan S, Hellstrom M, Lefere P, Mang T, Regge D, Stoker J, Taylor S, Laghi A, ESGAR CT Colonography Working Group. The second ESGAR consensus statement on CT colonography. Eur Radiol. 2013;23:720–9.CrossRef Neri E, Halligan S, Hellstrom M, Lefere P, Mang T, Regge D, Stoker J, Taylor S, Laghi A, ESGAR CT Colonography Working Group. The second ESGAR consensus statement on CT colonography. Eur Radiol. 2013;23:720–9.CrossRef
19.
Zurück zum Zitat van der Meulen MP, Lansdorp-Vogelaar I, Goede SL, Kuipers EJ, Dekker E, Stoker J, van Ballegooijen M. Colorectal cancer: cost-effectiveness of colonoscopy versus CT colonography screening with participation rates and costs. Radiology. 2018;287:901–11.CrossRef van der Meulen MP, Lansdorp-Vogelaar I, Goede SL, Kuipers EJ, Dekker E, Stoker J, van Ballegooijen M. Colorectal cancer: cost-effectiveness of colonoscopy versus CT colonography screening with participation rates and costs. Radiology. 2018;287:901–11.CrossRef
20.
Zurück zum Zitat Hassan C, Pickhardt PJ. Cost-effectiveness of CT colonography. Radiol Clin N Am. 2013;51:89–97.CrossRef Hassan C, Pickhardt PJ. Cost-effectiveness of CT colonography. Radiol Clin N Am. 2013;51:89–97.CrossRef
Metadaten
Titel
Computed tomography colonography versus colonoscopy for detection of colorectal cancer: a diagnostic performance study
verfasst von
Junping sha
Jun chen
Xuguang lv
Shaoxin liu
Ruihong chen
Zhibing zhang
Publikationsdatum
01.12.2020
Verlag
BioMed Central
Erschienen in
BMC Medical Imaging / Ausgabe 1/2020
Elektronische ISSN: 1471-2342
DOI
https://doi.org/10.1186/s12880-020-00446-7

Weitere Artikel der Ausgabe 1/2020

BMC Medical Imaging 1/2020 Zur Ausgabe

Update Radiologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.