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| ORIGINAL ARTICLE |
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| Year : 2015 | Volume
: 14
| Issue : 1 | Page : 25-30 |
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Focal Colonic FDG Activity with PET/CT: Guidelines for Recommendation of Colonoscopy
Tianye Liu1, Spencer Behr1, Sana Khan1, Robert Osterhoff2, Carina Mari Aparici1
1 Department of Radiology and Biomedical Imaging, University of California, San Francisco, California, USA
2 Department of Medicine, University of California, San Francisco, California, USA
| Date of Web Publication | 2-Feb-2015 |
Correspondence Address:
Tianye Liu
Department of Radiology and Biomedical Imaging, University of California, San Francisco, California
USA
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DOI: 10.4103/1450-1147.150524 PMID: 25709541 
 Abstract | | |
Focal 18 F-fluorodeoxyglucose (FDG) colonic activity can be incidentally seen in positron emission tomography/computed tomography (PET/CT) scans. Its clinical significance is still unclear. The purpose of this study was to assess the significance of focal FDG activity in PET/CT scans by correlating the imaging findings to colonoscopy results, and come up with some guidelines for recommendation of follow-up colonoscopy. A total of 133 patients who underwent both 18 F-FDG PET/CT for different oncological indications and colonoscopy within 3 months were retrospectively studied. Imaging, colonoscopy and pathology results were analyzed. Of the 133 FDG-PET/CT scans, 109/133 (82%) did not show focal colonic FDG activity, and 24/133 (18%) did. Of the 109/133 PET/CTs without focal colonic FDG activity, 109/109 (100%) did not have evidence of colon cancer after colonoscopy and histology. Of the 24/133 PET/CTs with focal colonic FDG activity, 10/24 (42%) had pathologic confirmation of colon cancer and 14/24 (58%) did not have evidence of colon cancer after colonoscopy and histological analysis. Sensitivity was 10/10 (100%), specificity 109/123 (89%), positive predictive value (PPV) 10/24 (42%) and negative predictive value (NPV) 109/109 (100%). Incidental focal 18 FDG activity in PET/CT imaging shows a high sensitivity, specificity and NPV for malignancy, with a not so high PPV of 42%. Although some people would argue that a 42% chance of malignancy justifies colonoscopy, this maybe is not possible in all cases. However, the high sensitivity of the test does not allow these studies to be overlooked. We provide our recommendations as per when to send patients with focal FDG colonic activity to have further characterization with colonoscopy. Keywords: Colorectal cancer, fluorodeoxyglucose, positron emission tomography
How to cite this article:
Liu T, Behr S, Khan S, Osterhoff R, Aparici CM. Focal Colonic FDG Activity with PET/CT: Guidelines for Recommendation of Colonoscopy. World J Nucl Med 2015;14:25-30 |
How to cite this URL:
Liu T, Behr S, Khan S, Osterhoff R, Aparici CM. Focal Colonic FDG Activity with PET/CT: Guidelines for Recommendation of Colonoscopy. World J Nucl Med [serial online] 2015 [cited 2020 Jan 26];14:25-30. Available from: http://www.wjnm.org/text.asp?2015/14/1/25/150524 |
| Introduction | |  |
Colorectal cancer is the third most commonly diagnosed cancer in the world. Around 60% of cases are diagnosed in developed countries. Globally more than 1 million people develop colorectal cancer every year. [1] Symptoms depend on the location of the tumor but the common warning signs include worsening constipation, blood in the stool, decrease in stool caliber, loss of appetite and weight. Risk factors include older age, male gender, obesity and smoking. [2],[3] Colonoscopy, the endoscopic examination of the colon, is regarded as the recommended standard for colorectal cancer screening because it both provides a visual diagnosis and grants the opportunity for biopsy or removal of suspected colorectal cancer lesions. [4]
Positron emission tomography (PET) is widely used in oncology. [5],[6] Incidental 18 F-fluorodeoxyglucose (FDG) diffuse and focal colon activity of multiple levels of intensity is incidentally seen in the 18 F-FDG-PET/computed tomography (CT) scans. Although diffuse activities are more confidently considered physiological, little information is available for the clinical significance of the focal activities in the colon. We therefore performed a study to assess the significance of incidental focal FDG activity in 18 F-FDG-PET/CT scans in the diagnoses of colorectal cancer by correlating the imaging findings to colonoscopy and pathology results.
| Materials and Methods | | |
This study was approved by the Institutional Review Board and the need for informed consent was waived. We performed a retrospective review of patients with 18 F-FDG-PET/CT scan and colonoscopy during the last 7 years (2006-2013). Those who had a colonoscopy within 3 months from their 18 F-FDG-PET/CT scan were included in the study.
Imaging technique
The 18 F-FDG-PET/CT studies were obtained using a discovery 64 slice PET/CT scanner from general electric (GE) with bismuth germanium oxide crystals. The patients were nil per os for 6 h prior to the test. After assessment of glucose levels, the patients with glucose level <140 mg/dL were intravenously administered with 10 mCi (370 MBq) of F 18 -FDG. 60 min later, they were taken to the scanner for imaging. A transmission scan (5 mm contiguous axial cuts) was obtained using an integrated multi-slice helical CT from vertex to mid-thighs. The acquisition was obtained with a one-slice overlap at the borders of the field of view to avoid artifacts, using 120 kV, and a 512 × 512 matrix size. Immediately after, and without moving the patient, and emission scan was obtained in three-dimensional-mode in 7-8 beds at 3 min/bed over the same anatomical regions. The PET emission scan was corrected using segmented attenuation data of the conventional transmission scan. A Gaussian filtering (6.4 mm) was performed for smoothing of images. The PET images were reconstructed with a standard iterative algorithm (ordered subsets expectation maximization, two iterative steps, 24 subsets) using (General Electric) software.
Imaging criteria
Two American Board of Nuclear Medicine (ABNM) certified physicians reviewed the 18 F-FDG-PET/CT scans. A scan was considered positive when "focal" FDG activity was identified in the colon and the activity was above the blood pool. A scan was considered negative when no "focal" FDG activity was identified in the colon, or the focal activity was below the blood pool level. The two ABNM certified physicians reviewing the 18 F-FDG-PET/CT scans and achieved a consensus in all cases.
Colonoscopy
In preparation for the colonoscopy, the patients' colons were cleansed. They were asked to drink clear liquid and not eat solid food for 3 days. During the colonoscopy examination, the colonoscope was inserted through the anus and gently advanced to the lowest part of the small intestines while the patient was sedated. Abnormal polypoid and flat lesions detected during colonoscopy were biopsied and sent for final pathological analysis.
Pathology
After histological analysis, a lesion submitted after colonoscopy was considered positive for malignancy in the following cases: Carcinomas, invasive adenomas, metastatic disease, primary malignancies like melanoma, and myeloproliferative processes infiltrating colonic mucosa. Hyperplastic polyps as well as tubulous, villous and tubulovillous polyps were not considered positive findings for malignancy.
| Results | | |
The retrospective review provided a total of 133 patients (57 males and 76 females) with a mean age of 58 years old (age range 10-87) who underwent both 18 F-FDG-PET/CT and colonoscopy within 3 months of the scan. Of these 133 FDG-PET/CT scans, 109/133 (82%) did not show focal colonic FDG activity, and 24/133 (18%) did.
Of the 109/133 PET/CTs without focal colonic FDG activity, all 109 (100%) did not have evidence of colon cancer after colonoscopy and histologic analysis. Of the 24/133 PET/CTs with focal colonic FDG activity, 10/24 (42%) had pathologic confirmation of colon cancer and 14/24 (58%) did not have evidence of colon cancer after colonoscopy and histological analysis.
The statistical analysis demonstrated a sensitivity of 10/10 (100%), specificity 109/123 (89%), positive predictive value (PPV) 10/24 (42%), negative predictive value (NPV) 109/109 (100%) [Table 1] and [Table 2].
| Discussion | | |
In this retrospective study comparing 18 F-FDG-PET/CT scans with colonoscopy/histology findings obtained within 3 months of the imaging study, only 18% (24/133) of the scans showed focal FDG activity in the colon. This finding suggests that the pattern of focal FDG activity in the colon (the one that may raise concern for malignancy) is not seen as frequently as the diffuse pattern (18% vs. 82%).
Of the 109 patients without focal FDG activity in the scans, 0/109 patients ended up having evidence of malignancy in the colonoscopy. These results suggest that 18 F-FDG-PET/CT has a very high NPV, in our series of 100%, to rule out colon cancer when no focal FDG colonic activity is seen. Therefore, the probability of having cancer in the colon that would have been picked up with colonoscopy in a patient with no focal FDG activity in the colon is remote.
Due to the retrospective nature of the study, some limitations exist. Selection bias, such as those involving not including patients who were not recommended for colonoscopy by their physicians could potentially be present.
In our study, hyperplastic polyps as well as tubulous, villous and tubulovillous polyps were not considered positive findings for malignancy. However, it is well known that the latter lesions are considered premalignant. Villous adenomas are the most likely type of polyp to become cancerous followed by tubulovillous adenomas. Villous adenomas >2 cm have 53% chance of containing cancer and tubulovillous adenomas >2 cm have 46% chance. [7] In our study, two tubulovillous adenomas were identified in the final pathology. One measured <2 cm and did not show focal FDG activity. The other one measured >2 cm (3.3 cm × 2.1 cm × 1.5 cm) and showed focal high-grade dysplasia in histology. Interestingly, the patient's FDG-PET/CT showed "focal" FDG activity with an maximum standardized uptake value (SUVmax) of 1.6. Although slightly above blood pool (SUVmax 1.2) the FDG activity was clearly associated with an anatomical abnormality. This finding was considered a false positive (FP) in this paper, however it raises the possibility of FDG-PET/CT being able to identify and/or have a role in the characterization of these premalignant lesions, and consider it advantageous to refer these patients for colonoscopy before possible malignant transformation.
Of the 24 patients with focal FDG activity in the colon, only 42% (10/24) had histological confirmation of malignancy [Figure 1], providing a PPV of 42%. This PPV doesn't justify the need to recommend colonoscopy to every patient with focal FDG activity in the colon. In ~ 58% of the cases, the study would be negative and resources would have been allocated unnecessarily [Figure 2]. However, considering that the sensitivity was 100% (10/10), this is obviously a pattern not to be dismissed. Therefore, a good compromise about when to recommend colonoscopy after visualization of focal FDG activity on PET/CT is required. | Figure 1: An example of true-positive focal-fluorodeoxyglucose (FDG) colonic activity in a positron emission tomography/computed tomography (PET/CT). (a) FDG-PET/ CT maximum intensity projection image showing intensely hypermetabolic wall thickening in the rectosigmoid colon (maximum standardized uptake value 9.6). (b-d) Respectively the (b) FDG images (c) CT images and (d) hybrid images of the malignancy
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 | Figure 2: An example of a false-positive focal-fluorodeoxyglucose (FDG) colonic activity in a positron emission tomography/computed tomography (PET/CT) in a patient with history of lymphoma. (a) FDG-PET/CT maximum intensity projection image showing focal FDG activity in the distal cecum (maximum standardized uptake value 7.6). No significant abnormalities were identified in the colonoscopy. (b-d) Respectively the (b) FDG images (c) CT images and (d) hybrid images of this region
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The SUVmax values of the 24 focal FDG colonic regions in this study ranged from 1.6 to 18.4. The SUVmax values of the 10 focal FDG colonic regions confirmed to be malignant ranged from 3.9 to 18.4, and the benign lesions from 1.6 to 13.3. Both, benign and malignant lesions in the colon show a very wide range, and seen in [Figure 3], there is significant overlap between SUVmax of benign and malignant lesions in the colon showing focal FDG activity. Therefore SUVmax cannot be used to allow differentiation between these malignant and benign lesions. | Figure 3: Maximum standardized uptake value comparison between benign and malignant lesions
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In one case [Figure 4], the FDG-PET/CT demonstrated a very intensely hypermetabolic lesion with SUVmax 15.3 in the rectosigmoid associated with marked wall thickening and luminal narrowing that was very suspicious for malignancy. A colonoscopy was recommended and surprisingly, the results of the colonoscopy were negative. In fairness, the patient was not very well prepared for the colonoscopy. However, the report clearly assessed the rectosigmoid as negative for malignancy. 15 days later the patient presented with a paralytic ileus and required surgery. During surgery, a colon cancer in the rectosigmoid colon (corresponding to the FDG-PET/CT images) was identified as the culprit lesion. The finding identified in the PET/CT was considered a true positive for this study since the histology results from the surgical procedure was obtained within a month from the scan [Table 3]. Colonoscopy, as with all other techniques, can produce false negative results. Therefore, in cases with high suspicion for malignancy in the imaging findings close, even with negative colonoscopy, close attention on follow-up should be recommended. | Figure 4: Fluorodeoxyglucose-positron emission tomography/computed tomography (FDG-PET/CT) demonstrating a intensely hypermetabolic lesion with maximum standardized uptake value 15.3 in the rectosigmoid colon associated with marked wall thickening and luminal narrowing, highly suspicious for malignancy. However, colonoscopy showed negative results. 15 days later the patient presented with a paralytic ileus and required surgery. A colonic mass was identified in the operating room in the location identified by the images. The mass was histologically confirmed to represent rectosigmoid adenocarcinoma. The finding identified in the FDG-PET/CT images was considered a true positive for this study since the histological results from the surgical procedure were obtained within a month from the scan. (a-c) Respectively the (a) FDG images (b) CT images and (c) fused images of the hypermetabolism
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There is a paucity of studies in the literature assessing the significance of colonic 'focal' FDG activity in the PET/CT scans. A retrospective study by Cho et al. enrolling 241 patients with FDG-PET/CT performed within 2 weeks of colonoscopy produced similar statistic results. The NPV (95.9%) was very high and similar to that of our study. As with our study, the PPV (51.6%) was the lowest value, though not as low as in our cohort. The low PPVs are consistent with the recognized high frequency of FP results in PET/CT performed for the detection of malignancy in the colon. [8] Sensitivity and NPV in our study were both 100% and similarly they were high in this study (89.1% and 95.9%, respectively). [9] A noteworthy difference in the imaging criteria is that our criteria for positive focal FDG was based on the comparison of focal FDG activity with blood pool activity, whereas Cho's study defined a positive criteria on imaging findings with SUVmax >3.5. As a consequence, our study has more FP cases and lower sensitivity since benign focal areas of FDG activity in colon with SUVmax as low as 1.6 were considered. Of interest, in our study all malignancies showed an SUVmax >3.9. Therefore, a focal SUVmax of 3.5-4 in the colon could be a good SUVmax cut-off for concerning malignancy.
Another retrospective study by Purandare et al. enrolling only 32 patients had PPV of 40%, which is very close to our PPV of 42% despite the lower number of patients included in their study. [10] Another retrospective study by Lee et al. with 195 oncology patients assessed concerning focal colonic FDG uptake, but confined only to the left-sided colon, and concluded that 18 F-FDG uptake by oncology patients to the left-sided colon warrant endoscopic verification because a significant portion (145/195) of the patients with focal 18 F-FDG uptake had advanced colonic neoplasm. [11] Although our study did not show similar findings, it is true that all the confirmed malignancies were identified between the splenic flexure and the anus.
A retrospective study by Rainis et al. [12] with only 56 patients, showed that out of 21 patients with positive focal FDG-PET/CT only 3 showed malignancy while the rest were benign findings. The PPV for malignancy (14%) was lower than that of our study, and the authors conclude that many nonmalignant abnormalities such as polyps and adenomas were found by FDG-PET/CT. [12] This is not consistent with our findings. Out of 18 polyps identified on colonoscopy in our series (3 hyperplastic, 13 tubular adenomas and 2 tubulovillous adenomas) only one, a 3.3 × 2.1 × 1.5 cm tubulovillous adenoma with focal high-grade dysplasia, showed very mild associated FDG activity.
Both the study by Purandare et al. and another similar retrospective study by Putora et al. concluded that malignancy could not be ruled out based on SUVmax alone because the differences of SUVmax between the premalignant adenomatous polyps and the malignant lesions was not significant. [10],[13] This is consistent with our observation of the SUVmax in our study. A comparison between benign and malignant SUVmax values by Roh et al. also concluded that SUVmax should not be used as an independent indicator for diagnosing benign and malignant lesions for the same reason. However, the study did note that malignant lesions tend to have higher SUVs and proposed a cut-off value of 4.95 for cases that may be presumed as higher possibility of being malignant. [14] As discussed above, in our series, 2 confirmed malignancies showed an SUVmax as low as 3.9. Therefore, a more conservative cut-off is required.
| Conclusion | | |
Incidental focal colonic FDG activity in 18 F-FDG-PET/CT scans is not a frequent finding, in our series occurring in only 18% of the scans. This pattern of focal colonic FDG activity show a high sensitivity, specificity and NPV for colonic malignancy, but a relatively lower PPV of 42%. Therefore, although a PPV of 42% may be considered justifiable for colonoscopy, it is not recommended to confirm every focus of FDG activity in the colon with a colonoscopy. However, due to its considerably high sensitivity of 100%, it is certainly a pattern not to be dismissed. SUVmax by itself is not a good independent indicator. Therefore, a good compromise to recommend colonoscopy after visualization of focal FDG activity on - PET/CT is required. Our recommendations are: Patients with "focal" FDG activity in the colon and one of the following is recommended to undergo colonoscopy for further assessment: High risk of colon cancer, prior history of colon cancer, concerning associated anatomical changes, focal FDG activity at site of prior anastomosis for cancer (with or without concerning associated anatomical changes), and focal FDG activity in the "same location" seen in a prior FDG-PET/CT scan. Otherwise, incidental focal FDG activity in the colon could be considered an incidental finding and attention on follow-up PET/CT recommended to confirm resolution.
| References | | |
| 1. | Cunningham D, Atkin W, Lenz HJ, Lynch HT, Minsky B, Nordlinger B, et al. Colorectal cancer. Lancet 2010;375:1030-47.  |
| 2. | Yamada T, Alpers DH, Kalloo AN, Powell DW. Principles of Clinical Gastroenterology. 5 th ed. Chichester: Wiley-Blackwell; 2008. |
| 3. | Chang LC, Wu MS, Tu CH, Lee YC, Shun CT, Chiu HM. Metabolic syndrome and smoking may justify earlier colorectal cancer screening in men. Gastrointest Endosc 2014;79:961-9. |
| 4. | Maciosek MV, Solberg LI, Coffield AB, Edwards NM, Goodman MJ. Colorectal cancer screening: Health impact and cost effectiveness. Am J Prev Med 2006;31:80-9. |
| 5. | Fletcher JW, Djulbegovic B, Soares HP, Siegel BA, Lowe VJ, Lyman GH, et al. Recommendations on the use of 18F-FDG PET in oncology. J Nucl Med 2008;49:480-508. |
| 6. | Griffeth LK. Use of PET/CT scanning in cancer patients: Technical and practical considerations. Proc (Bayl Univ Med Cent) 2005;18:321-30. |
| 7. | Itzkowitz SH, Rochester J. Colonic polyps and polyposis syndromes. In: Feldman M, Friedman LS, Brandt LJ. editors. Sleisenger and Fordtran′s Gastrointestinal and Liver Disease. 8 th ed. Vol. 2. Philadelphia: Saunders/Elsevier; 2006. p. 2713-57. |
| 8. | Wang G, Lau EW, Shakher R, Rischin D, Ware RE, Hong E, et al. How do oncologists deal with incidental abnormalities on whole-body fluorine-18 fluorodeoxyglucose PET/CT? Cancer 2007;109:117-24. |
| 9. | Cho SH, Kim SW, Kim WC, Park JM, Yoo IeR, Kim SH, et al. Incidental focal colorectal 18F-fluorodeoxyglucose uptake on positron emission tomography/computed tomography. World J Gastroenterol 2013;19:3453-8. |
| 10. | Purandare NC, Gawade SK, Puranik AD, Agrawal A, Shah S, Rangarajan V. Etiology and significance of incidentally detected focal colonic uptake on FDG PET/CT. Indian J Radiol Imaging 2012;22:260-6. [ PUBMED]  |
| 11. | Lee C, Koh SJ, Kim JW, Lee KL, Im JP, Kim SG, et al. Incidental colonic 18F-fluorodeoxyglucose uptake: Do we need colonoscopy for patients with focal uptake confined to the left-sided colon? Dig Dis Sci 2013;58:229-35. |
| 12. | Rainis T, Kaidar-Person O, Keren D, Lavy A, Keidar Z. Correlation between incidental FDG PET/CT colorectal observations and endoscopic and histopathological results. Oncol Lett 2014;7:479-82. |
| 13. | Putora PM, Müller J, Borovicka J, Plasswilm L, Schmidt F. Relevance of incidental colorectal FDG-PET/CT-enhanced lesions. Onkologie 2013;36:200-4. |
| 14. | Roh SH, Jung SA, Kim SE, Kim HI, Lee MJ, Tae CH, et al. The clinical meaning of benign colon uptake in (18) F-FDG PET: Comparison with colonoscopic findings. Clin Endosc 2012;45:145-50. |
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3]
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