Gut 2006;55:1007-1011
GASTROINTESTINAL CANCER
Positron emission tomography scanning is not superior to whole body multidetector helical computed tomography in the preoperative staging of colorectal cancer
1 Division of Diagnostic Radiology, Shizuoka Cancer Centre Hospital, Shizuoka, Japan
2 Division of Colorectal Surgery, Shizuoka Cancer Centre Hospital, Shizuoka, Japan
Correspondence to:
Dr H Furukawa
Division of Diagnostic Radiology, Shizuoka Cancer Centre Hospital, 1007, Nagaizumi-cho, Suntogun, Shizuoka, 411-8777, Japan; h.furukawa{at}scchr.jp
Background: The role of positron emission tomography with the glucose analogue [18F] fluoro-2-deoxy-D-glucose (FDG-PET) in the initial staging of disease in patients with primary colorectal cancer (CRC) has not been adequately assessed.
Aims: To evaluate the additional value of FDG-PET as a staging modality, complementary to routine multidetector row computed tomography (MDCT) in patients with CRC.
Methods: Forty four patients with CRC underwent preoperative MDCT and FDG-PET. The accuracy of intraoperative macroscopic staging was also investigated compared with histopathological diagnosis. All FDG-PET images were evaluated with respect to detectability of the primary tumour, lymph node involvement, and distant metastases. Both MDCT and FDG-PET diagnoses and treatment plan were compared with surgical and histopathological results.
Results: Thirty seven patients underwent surgery. Tumour detection rate was 95% (42/44) for MDCT, 100% (44/44) for FDG-PET, and 100% (37/37) for intraoperative macroscopic diagnosis. Pathological diagnosis of T factor was T1 in five, T2 in four, T3 in 24, and T4 in four cases. Concordance rate with pathological findings of T factor was 57% (21/37) for MDCT and 62% (23/37) for macroscopic diagnosis. Lymph node involvement was pathologically positive in 19 cases. Regarding N factor, overall accuracy was 62% (23/37) for MDCT, 59% (22/37) for FDG-PET, and 70% (26/37) for macroscopic diagnosis. For all 44 patients, FDG-PET findings resulted in treatment changes in only one (2%) patient.
Conclusion: FDG-PET is not superior to routine MDCT in the initial staging of primary CRC.
Abbreviations: PET, positron emission tomography; FDG-PET, [18F] fluoro-2-deoxy-D-glucose-positron emission tomography; CRC, colorectal cancer; CT, computed tomography; MDCT, multidetector row computed tomography
Keywords: positron emission tomography; colorectal surgery; spiral computed tomography; colorectal neoplasms; neoplasm staging
Relevant Article
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
Gut 2006 55: 905.
This article has been cited by other articles:
-
Nakamoto, Y., Togashi, K., Kaneta, T., Fukuda, H., Nakajima, K., Kitajima, K., Murakami, K., Fujii, H., Satake, M., Tateishi, U., Kubota, K., Senda, M.
(2009). Clinical Value of Whole-body FDG-PET for Recurrent Gastric Cancer: A Multicenter Study. Jpn J Clin Oncol
39: 297-302
[Abstract] [Full Text] -
Herbertson, R. A., Lee, S. T., Tebbutt, N., Scott, A. M.
(2007). The expanding role of PET technology in the management of patients with colorectal cancer. Ann Oncol
18: 1774-1781
[Abstract] [Full Text] -
(2006). Preoperative PET Scanning in Colorectal Cancer Isn't Useful. JWatch Gastroenterology
2006: 2-2
[Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
