Is (18)F-fluorodeoxyglucose positron emission tomography in recurrent colorectal cancer a contribution to surgical decision making?
- PMID: 11036130
- DOI: 10.1016/s0002-9610(00)00406-2
Is (18)F-fluorodeoxyglucose positron emission tomography in recurrent colorectal cancer a contribution to surgical decision making?
Abstract
Background: Accuracy of (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) and contribution to surgical decision making in recurrent or metastatic colorectal cancer were evaluated.
Methods: One hundred whole-body PET tests in colorectal cancer patients (1994 to 1998) were compared with computed tomography (CT), liver ultrasonography, and carcinoembryonic antigen (CEA) test. Mean follow-up was 12 months.
Results: Sensitivity, specificity, and accuracy of FDG-PET for malignant findings were, respectively, 98%, 90% and 95%; for 87 CT scans, 91%, 72%, and 82%; for 98 CEA tests, 76%, 90%, and 82%; for detection of liver metastases with PET, 100%, 99%, and 99%; and for 68 ultrasound tests, 87%, 96%, and 93%. PET accuracy for local recurrence was 96%. Additional information was provided by PET in 86% of cases (abdomen, thorax, liver). PET influenced surgical decisions in 61% of cases.
Conclusion: FDG-PET adds relevant accuracy to the conventional staging of patients with colorectal cancer and may cost-effectively help to select the appropriate treatment.
Similar articles
-
Diagnostic value of (18)F-FDG PET/CT as first choice in the detection of recurrent colorectal cancer due to rising CEA.Cancer Imaging. 2015 Aug 13;15(1):11. doi: 10.1186/s40644-015-0048-y. Cancer Imaging. 2015. PMID: 26263901 Free PMC article.
-
[Evaluation of positron emission tomography by using F-18-fluorodeoxyglucose in diagnosis of recurrent colorectal cancer].Pol Merkur Lekarski. 2004;17 Suppl 1:63-6. Pol Merkur Lekarski. 2004. PMID: 15603351 Clinical Trial. Polish.
-
Clinical impact of 18F-FDG-PET in the suspicion of recurrent colorectal cancer based on asymptomatically elevated serum level of carcinoembryonic antigen (CEA) in Taiwan.Hepatogastroenterology. 2006 May-Jun;53(69):348-50. Hepatogastroenterology. 2006. PMID: 16795969
-
FDG PET/CT in colorectal cancer.Rev Esp Med Nucl Imagen Mol (Engl Ed). 2020 Jan-Feb;39(1):57-66. doi: 10.1016/j.remn.2019.09.009. Epub 2019 Nov 24. Rev Esp Med Nucl Imagen Mol (Engl Ed). 2020. PMID: 31776063 Review. English, Spanish.
-
Role of FDG-PET in the diagnosis and treatment of colorectal liver metastases.Expert Rev Anticancer Ther. 2004 Aug;4(4):607-13. doi: 10.1586/14737140.4.4.607. Expert Rev Anticancer Ther. 2004. PMID: 15270664 Review.
Cited by
-
Imaging and Metabolic Diagnostic Methods in the Stage Assessment of Rectal Cancer.Cancers (Basel). 2024 Jul 16;16(14):2553. doi: 10.3390/cancers16142553. Cancers (Basel). 2024. PMID: 39061192 Free PMC article. Review.
-
18F-Fluoro-2-deoxyglucose positron emission tomography in the evaluation of gastrointestinal malignancies.Gut. 2003 Jun;52 Suppl 4(Suppl 4):iv23-9. doi: 10.1136/gut.52.suppl_4.iv23. Gut. 2003. PMID: 12746265 Free PMC article. Review.
-
What is the most accurate whole-body imaging modality for assessment of local and distant recurrent disease in colorectal cancer? A meta-analysis : imaging for recurrent colorectal cancer.Eur J Nucl Med Mol Imaging. 2011 Aug;38(8):1560-71. doi: 10.1007/s00259-011-1785-1. Epub 2011 Apr 6. Eur J Nucl Med Mol Imaging. 2011. PMID: 21468765 Free PMC article.
-
Use of FDG-PET or PET/CT to detect recurrent colorectal cancer in patients with elevated CEA: a systematic review and meta-analysis.Int J Colorectal Dis. 2013 Aug;28(8):1039-47. doi: 10.1007/s00384-013-1659-z. Epub 2013 Feb 14. Int J Colorectal Dis. 2013. PMID: 23407908
-
Efficacy of preoperative combined 18-fluorodeoxyglucose positron emission tomography and computed tomography for assessing primary rectal cancer response to neoadjuvant therapy.J Gastrointest Surg. 2007 Aug;11(8):961-9; discussion 969. doi: 10.1007/s11605-007-0170-7. J Gastrointest Surg. 2007. PMID: 17541799
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources