- Open Access
FDG-PET scan in patients with clinically and/or radiologically suspicious colorectal cancer recurrence but normal CEA
© Sarikaya et al; licensee BioMed Central Ltd. 2007
- Received: 27 March 2007
- Accepted: 07 June 2007
- Published: 07 June 2007
Although frequently used for tumor surveillance, the sensitivity of carcinoembryonic antigen (CEA) to detect recurrent colorectal cancer (CRC) is not optimal. Fluorine 18-fluoro-2-deoxy-glucose-positron emission tomography (18F FDG-PET) scans promise to improve recurrent CRC detection. We aimed to review PET scans of patients with clinically and/or radiologically suspicious tumor recurrence but normal CEA.
A retrospective review of an electronic database of 308 patients with CRC who had PET scans was performed. Only PET studies of patients with normal CEAs and suspected tumor recurrence who had pathological verification were selected for further analysis. Thirty-nine patients met the inclusion criteria.
PET was positive in 26 patients (67%) and normal in 13 (33%). Histopathologic evidence of tumor recurrence was seen in 27 of the 39 patients (69%). When correlated with histopathology, PET was true positive in 22 patients, false positive in 4, true negative in 8 and false negative in 5. Overall, the accuracy of PET was 76.9%, negative predictive value (NPV) was 61.5%, and positive predictive value (PPV) was 84.6%. PPV value of PET for liver metastases was 88.8% compared to 73.3% for local recurrence. In two patients with confirmed recurrence, CEA became positive 2 months after PET scan indicating earlier detection of disease with PET. The false positive PET findings were mainly in the bowel and were secondary to acute/chronic inflammation and granulation tissue. In 3 patients with false negative PET, histopathology was consistent with mucinous adenocarcinoma.
PET yields high PPV for recurrent CRC, particularly for liver metastases, in spite of normal CEA levels and should be considered early in the evaluation of patients with suspected tumor recurrence.
- Positron Emission Tomography
- Positive Predictive Value
- Standardize Uptake Value
- Positive Positron Emission Tomography
- Negative Positron Emission Tomography
Colorectal cancer (CRC) is the third most common cause of cancer in both men and in women in the United States. The five-year overall survival rates is 64% . Local recurrence rate is relatively high despite radical curative surgery and up to 50% of patients with local recurrence may benefit from surgery.
Early detection and treatment of tumor recurrence is the only hope for long-term survival. Although carcinoembryonic antigen (CEA) is the most frequently used tumor marker, it has low sensitivity in the early detection of recurrent colorectal cancer (CRC). Conventional imaging methods such as Computed Tomography (CT) and Magnetic Resonance Imaging (MR) have limited value in differentiating post-surgical changes from local tumor recurrence. Positron Emission Tomography (PET) and, particularly, Positron Emission Tomography/Computed Tomography (PET/CT) are widely accepted imaging methods in the management of a wide variety of cancers, including CRC. Many studies have demonstrated the value of PET in the detection of CRC recurrence in patients with rising CEA in the post-operative period [2–5]. Studies have also demonstrated the superiority of PET over CT in the detection of local CRC recurrence as well as metastatic disease [6–11]. The role of PET in patients with normal CEA levels, however, is not clear.
In this study, we aimed to analyze the value of FDG-PET scans in patients with normal CEA levels but clinical or radiological findings suspicious for tumor recurrence.
A retrospective review of our electronic database of 308 patients with CRC imaged by PET or PET/CT between January 2003 and December 2005 was performed to select and analyze PET scan findings of patients who had normal CEA but clinically and/or radiologically suspicious findings for tumor recurrence. Only patients with correlative histopathological data were included. The institutional review board allowed an exempt retrospective review of the cancer PET database, and informed consent was waived. The normal range for CEA in our clinical laboratory was 0–5.0 ng/mL (chemiluminescent immunoassay). Although the CEA levels were available and normal on all patients at the time of their evaluation for suspicion of recurrent CRC, initial baseline CEA levels taken at a time before their initial treatment for their originally diagnosed CRC were available in only 10 patients (with initial baseline CEA level within normal range in seven patients and elevated in three patients).
PET studies were performed on Siemens Biograph 16 PET/CT and HR plus Siemens CTI PET camera (CTI, Inc, Knoxville, TN). The patients fasted approximately 6 hours prior to intravenous injection of 370–555 MBq (10–15 mCi) of Fluorine 18-fluoro-2-deoxy-glucose (18F FDG). Blood glucose levels were checked prior to the injection of 18F FDG. Studies were performed only when blood glucose levels did not exceed 150 mg/dL. The imaging started approximately 60 minutes following intravenous injection of 18F FDG. For the PET/CT camera, first a scout view was obtained with 30 mAs and 130 kVp followed by a spiral CT scan with 130 mAs, 130 kVp, 5-mm scan width, and 12-mm feed per rotation without any specific breath-holding instructions. No IV or oral contrast was given to the patients for acquisition of the CT images. Imaging area was from skull base to proximal femora. PET scanning was performed immediately after acquisition of the CT images without changing the patient position with 2–4 minutes per bed acquisition time. PET images were corrected for attenuation on the basis of the CT data, and iterative reconstruction algorithms were used for reconstruction. For the PET only camera, image acquisition time of 10 minutes per bed by using 40% transmission and 60% emission protocol was used. PET images were corrected for attenuation on the basis of the transmission image data, and iterative reconstruction algorithms were used for reconstruction. PET images were evaluated by two board-certified nuclear medicine physicians (IS and NCH). PET scan was considered positive or suspicious when abnormal non-physiologic metabolic activity was identified. Focal hypermetabolic activity within the liver greater than adjacent normal liver was considered abnormal. Isometabolic liver lesions (metabolic activity equal to liver) were only identified with the help of CT in patients with PET/CT scan. Diffuse mild activity in the bowel was considered normal physiologic uptake. Quantification of the tumor metabolic activity was obtained using the Standardized Uptake Value (SUV) normalized to body weight. Mean ± SD of maximum-pixel SUV (SUVmax) of the lesions were calculated. The significance of SUVmax between false positive and true positive lesions were compared by t-test. A P-value of less than or equal to 0.05 was considered statistically significant.
Mean age [range (year)]
Mean time interval from initial treatment to PET scan [range (months)]
Mean time interval from last treatment to PET scan [range (months)]
PET and histopathological findings in 26 patients with positive PET scan
Location of RCRC
MD invasive adeno ca
Colon SD adeno ca met
Colon adeno ca met
MD mucinous adeno ca
Colon adeno ca met
MPD invasive adeno ca
MD invasive adeno ca
MPD invasive adeno ca
Colon IT adeno ca met
MD invasive adeno ca
Colon adeno ca met
Colon adeno ca met
Colon adeno ca met
MD adeno ca met
MD adeno ca
Colon adeno ca met
Colon adeno ca met
MD adeno ca
MD adeno ca
Right Colon/A LN/Liver
Colon adeno ca met
MD adeno ca
MD mucinous adeno ca
MD mucinous adeno ca
Focal foreign body reaction
In all patients with negative PET and negative pathology results, follow-up CEA values were available. In six of these patients, follow-up CEA values were normal (mean follow-up time 18.8 months, range: 4–41 months). In two patients, follow-up CEA level increased (mean follow-up time 3 months, range: 2–6 months).
PET and PET/CT results were evaluated separately. PET was true positive in 16 patients, false negative in three patients, and true negative in eight patients. PET/CT was true positive in six patients, false positive in four patients, and false negative in two patients. There was no false positive result with PET and no true negative result with PET/CT. The accuracy of PET and PET/CT was 88.8% and 50%, respectively.
Mean SUVmax ± standard deviation (SD) in true positive and false positive PET lesions based upon location of PET positive lesions.
True Positive PET
False Positive PET
5.4 ± 1.8 (3.1–8.2)
6.06 ± 3.5 (1.8–12)
8.5 ± 5.5 (4.5–16.7)
4.2 ± 1.7 (2–9–6.3)
5.25 ± 4.87 (1.8–8.7)
5.05 ± 1.48 (4–6.1)
5.51 ± 2.73 (1.8–12)
6.75 ± 5.1 (3.1–16.7)
Approximately 70% of patients with newly diagnosed CRC are suitable for a curative resection, but up to 50% of patients recurrence develops usually within two years of surgery [12–14]. Ten to 50% of local recurrences may be suitable for surgical resection [12–20]. In patients with liver metastasis hepatic resection in properly selected patients offers up to a 30% chance of cure . Early detection and prompt treatment of recurrence improves survival. Although CEA is used frequently in the post-operative follow-up period, its sensitivity for early detection of CRC recurrence is less than desirable . Moertel et al. reported that CEA has a sensitivity of 59% in the detection of CRC recurrence . CEA is also not specific for colorectal cancer. A wide variety of non-neoplastic conditions, such as smoking and liver and gastrointestinal diseases, may cause elevation in CEA. The use of PET as part of the diagnostic work-up of patients with rising CEA is well defined. However, there is a paucity of data concerning its role in patients with suspected CRC recurrence and normal CEA. We have shown that PET can be reliably applied in such patients to allow for earlier detection and management of recurrent CRC.
PET is a functional/metabolic imaging technique which has been widely used in the diagnosis, staging, and management of a wide variety of tumors. The most commonly used PET agent in oncology is 18F FDG, a positron-labeled non-physiologic analog of glucose. Malignant tumors avidly accumulate FDG because of accelerated glucose metabolism and increased rate of glucose transport and utilization in malignant cells. FDG in the blood is transported into the cells via glucose transporters and phosphorylated to FDG-6-phosphate by hexokinase. This is thought to occur more readily in tumors due to overexpression of the glucose transporters GLUT1 and GLUT3 and higher levels of hexokinase in malignant cells . Because Glucose-6-phosphatase enzyme is low in most of the tissues and tumors, FDG-6-phosphate cannot be dephosphorylated to FDG. Therefore, FDG-6-phosphate cannot cross the cell membrane and is trapped in the cell. As well, FDG-6-phosphate cannot be utilized in the metabolic steps of glycolysis resulting in accumulation of the radioactive tracer.
Many studies have demonstrated that FDG-PET has high sensitivity and specificity in the detection of tumor recurrence in patients with rising tumor markers in the absence of a known source by anatomical imaging methods [2–5]. A meta-analysis determined the overall sensitivity of 97% and specificity of 76% for FDG PET for detecting recurrent CRC . Studies have also demonstrated that FDG PET is more sensitive than CT for the detection of recurrent CRC [6–11]. PET was found to be superior to CT in the differentiation of fibrotic scar tissues from locally recurrent tumor . The accuracy of PET for locally recurrent disease was reported as 95% which was superior to pelvic-CT (65%) . PET is more sensitive than CT in detecting liver metastases and defining the number of the lobes involved. Arulapalam et al. reported the sensitivity of PET and CT as 100% and 45%, respectively, in the detection of liver metastasis . Similar to CT, MRI also has limitations in the differentiation of fibrotic scar from local recurrence. Although there is increasing use of dynamic contrast-enhanced MR, it is not clear yet whether it is superior to PET in the detection of recurrence. Contrast-enhanced liver MRI and whole-body FDG-PET were comparable in the detection of patients with liver metastases . PET provided additional information about extrahepatic disease. PET is a valuable imaging method to differentiate isolated resectable recurrence from disseminated metastatic disease to select patients who would benefit from surgery . Studies have also compared PET and PET/CT in the detection of CRC recurrence. The sensitivity, specificity and overall accuracy of PET were 80%, 69%, and 75%, respectively, compared with 89%, 92%, and 90%, respectively, for PET/CT . Another study demonstrated superiority of PET/CT over PET in differentiating malignant from benign lesions and physiologic activities . The most common cause for false-positive interpretation of PET findings was physiologic FDG uptake in pelvic organs.
In our study, histopathological analysis following PET scan demonstrated tumor recurrence or metastasis in 27 of 39 patients who have normal CEA but clinically and/or radiologically suspicious tumor recurrence. Twelve patients were tumor free. PET was true positive in 22 patients and true negative in eight patients. The accuracy of PET was 76.9%. Our results demonstrated that PET was most accurate for liver metastases with a positive predictive value 88.8%. For local recurrence, PET had PPV of 73.3%. PET was false negative in five patients. In three of these patients pathology was consistent with mucinous carcinoma with signet cells. Consistent with our findings, it has been reported that the sensitivity of FDG-PET imaging for detection of mucinous carcinoma is significantly lower than in nonmucinous carcinoma (58% and 92%, respectively) . PET was false positive in four patients. False positive PET lesions were mainly in the bowel and were secondary to infectious or inflammatory/granulomatous processes. False-positive findings with FDG-PET in colorectal region are not uncommon . Increased FDG uptake is observed at recent incision and biopsy sites, around drainage tubes and catheters, and at colostomy sites, as well as in association with colitis, abscesses, fistulas, diverticulitis, and in some benign adenomas. This is because of increased glucose use in activated macrophages, neutrophils, and fibroblasts within infectious, inflammatory, and granulomatous tissues. Normal FDG uptake in the gastrointestinal tract may also cause difficulty to differentiate normal physiologic uptake from recurrent tumor.
There are many factors affecting the serum concentration of CEA, including tumor location, proximity to large vessels, degree of de-differentiation, access to portal circulation, tumor distribution, and tumor burden. Previously Moertel et al reported the inadequacy of CEA for early detection of tumor recurrence . Only 25% of the patients had abnormal CEA levels although most patients had symptoms of recurrence for several months in their study. In two of our patients, CEA became positive 2 months after PET scan, suggesting that PET can show tumor recurrence earlier than CEA elevation. In our study, the lesion size was measured in focal solitary liver metastases in six patients. The tumor size ranged from 10 mm to 30 mm. However, our data is not sufficient to find the smallest tumor volume where PET can be positive while CEA negative. There are also many other factors in addition to tumor size affecting CEA level. However, we assume that given directly imaging the tumor and high glucose metabolism in tumor tissue, as well as current high-resolution PET/CT cameras, it is expected that FDG-PET may detect tumor recurrence before significant increase in CEA level.
Although PET facilitates the evaluation of metabolic characteristics of tumors, it is limited in its ability to visualize anatomical structures. A PET/CT camera is the combination of PET and CT cameras which allows more accurate registration of metabolic findings in tumor with anatomical findings, adding further information to the diagnosis and staging of tumors. In PET/CT cameras, CT is also used for attenuation correction of PET images which significantly reduces imaging time. In our study, the accuracy of PET/CT was found to be lower than PET alone. However, given the smaller number of exams performed by PET/CT than by PET alone, this determination of accuracy may not reliably reflect the actual accuracy of PET/CT versus PET alone.
Our study had several potential limitations. The first potential limitation was our small sample size which may have limited the robustness of our study in terms of statistics. The second potential limitation was the retrospective nature of our study. Because of its retrospective nature, we were unable to obtain baseline clinical and laboratory data in some of the patients. The third potential limitation was the pooled nature of the PET and PET/CT data, given that different attenuation correction algorithms were used in these two imaging methods. However, this issue would be of more concern had we compared PET SUVmax to PET/CT SUVmax in the same given patient. In defense of this third potential limitation, there is recently published study pooling PET and PET/CT SUV results . The fourth potential limitation was our inability to use oral contrast for the combined PET/CT studies, since some data is available which demonstrates that low density oral contrast administration during combined PET/CT studies further increases accuracy.
Although PET is commonly used to localize tumor recurrence in cases with elevated CEA, our results indicate that PET is also valuable to detect tumor recurrence in selected cases who have normal CEA but clinically and/or radiologically suspicious tumor recurrence. The PPV of PET is high, particularly in detecting liver metastases. While PET may not be practical for routine surveillance for all patients with CRC, it should be utilized in select cases where CEA is not reliable, such as tumors known to not secrete CEA. PET should also be utilized at the first sign of suspected recurrence to determine the extent of disease.
Preliminary data from this paper were previously presented as a poster (poster number 1648) in the Scientific Poster Session at the 54th Annual Meeting of the Society of Nuclear Medicine (SNM) on June 5, 2007 in Washington, DC.
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