Gastroenterology

Gastroenterology

Volume 125, Issue 3, September 2003, Pages 688-695
Gastroenterology

Clinical-alimentary tract
Computerized tomographic colonography: performance evaluation in a retrospective multicenter setting1 ,

https://doi.org/10.1016/S0016-5085(03)01058-8Get rights and content

Abstract

Background & Aims: No multicenter study has been reported evaluating the performance and interobserver variability of computerized tomographic colonography. The aim of this study was to assess the accuracy of computerized tomographic colonography for detecting clinically important colorectal neoplasia (polyps ≥10 mm in diameter) in a multi-institutional study. Methods: A retrospective study was developed from 341 patients who had computerized tomographic colonography and colonoscopy among 8 medical centers. Colonoscopy and pathology reports provided the standard. A random sample of 117 patients, stratified by criterion standard, was requested. Ninety-three patients were included (47% with polyps ≥10 mm; mean age, 62 years; 56% men; 84% white; 40% reported colorectal symptoms; 74% at increased risk for colorectal cancer). Eighteen radiologists blinded to the criterion standard interpreted computerized tomography colonography examinations, each using 2 of 3 different software display platforms. Results: The average area under the receiver operating characteristic curve for identifying patients with at least 1 lesion ≥10 mm was 0.80 (95% lower confidence bound, 0.74). The average sensitivity and specificity were 75% (95% lower confidence bound, 68%) and 73% (95% lower confidence bound, 66%), respectively. Per-polyp sensitivity was 75%. A trend was observed for better performance with more observer experience. There was no difference in performance across software display platforms. Conclusions: Computerized tomographic colonography performance compared favorably with reported performance of fecal occult blood testing, flexible sigmoidoscopy, and barium enema. A prospective study evaluating the performance of computerized tomography colonography in a screening population is indicated.

Section snippets

Study patients

After approval of this study by the Institutional Review Board of the American College of Radiology and by the National Cancer Institute Cancer Therapy Evaluation Program, 8 institutions submitted log forms listing 341 CT colonography examinations performed from January 1997 through April 2000 at their institution. The inclusion criteria were as follows: informed consent and institutional review board approval for sharing CT colonography data, clinically relevant CT acquisition parameters of a

Results

A total of 194 lesions were proven at pathology, colonoscopy, or both among the 93 patients in the study sample: 17 (18%) had no lesions, 15 (16%) had only lesions <5 mm in diameter, 17 (18%) had at least 1 lesion between 5 and 10 mm in diameter, and 44 (47%) had at least 1 lesion ≥10 mm in diameter. Lesions ranged in size from 3 to 75 mm (median, 5 mm). Thirty patients (32%) had 1 lesion, 22 (24%) had 2 lesions, and 24 (26%) had ≥3 lesions; the maximum number of lesions per patient was 12.

Discussion

This, the first published multicenter study evaluating the performance of CT colonography, marks an important milestone in the development and future evaluation of this imaging technique. Multicenter trials such as this one are critical in determining whether a technology is ready to be applied to the population or whether it requires further study. This retrospective study in particular serves to determine whether an additional prospective multicenter trial evaluating the performance of CT

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    Supported by the American College of Radiology Imaging Network through National Institutes of Health/National Cancer Institute Awards CA80098 and CA79778.

    1

    Vital Images Inc. has supported research at UCLA (to D. S. K. L., J. A. B., and E. G. M.). Monex provided support (to M. M.). GE Medical Systems provided software license and research support (to C. D. J., J. A. B., and A. H. D.). Voxar, Inc. produces products that compete with products listed in this paper (to M. A. B.).

    The study design was approved by the National Cancer Institute Cancer Therapy Evaluation Program. Computerized tomographic colonography examinations for American College of Radiology Imaging Network Protocol A6656 were submitted by E. G. McFarland, Mallinckrodt Institute of Radiology, St. Louis, Missouri; M. Zalis, Massachusetts General Hospital, Boston, Massachusetts; C. D. Johnson, Mayo Clinic, Rochester, Minnesota; M. Macari, New York University, New York, New York; D. Lu, University of California, Los Angeles, California; A. H. Dachman, University of Chicago, Chicago, Illinois; M. Morrin, Beth Israel/Deaconess Hospitals, Boston, Massachusetts; and J. Yee, Veterans Administration Hospital, San Francisco, California. Workstations for performing computerized tomographic colonography interpretations were loaned to the American College of Radiology (ACR) by General Electric, Vital Images, and the Mayo Clinic. Each provided technical support for installation at the ACR. Computerized tomographic colonography examinations were removed and workstations returned after the study interpretations were completed.

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