Joint Program in Nuclear Medicine
Esophageal Carcinoma and F-18 FDG PET Imaging
Pritinder K. Thind, MD
Alan J. Fischman, MD PhD
May 16, 2000
Presentation
A 60 year old male experienced swallowing difficulty 2 years prior to the index presentation.
Endoscopy demonstrated carcinoma in situ with extensive ulceration. At surgery, adenocarcinoma with retroperitoneal nodal metastases was found. The patient was treated with multiple cycles of chemotherapy. His prior risk factors included smoking (45 pack years), alcohol (several vodkas per day). He presented at the current time for evaluation of disease status.
Imaging Findings
Coronal images and sagital images of an F-18 fluorodeoxyglucose, FDG, PET are shown. There are multiple hypermetabolic foci in the mediastinum (superior mediastinum, right paratrcheal region, left hilum and AP window), distal 1/2 of the esophagus, periportal region, right adrenal gland and the splenic hilum (arrows on coronal images,
arrows on sagital images). These foci correlated with the CT scan abnormalities (superior mediastinal node in the prevascular region - with arrow, AP window node - with arrow, thickened esophagus - with arrow, and splenic hilum - with arrow).
Discussion
Treatment and Outcome:
- Fewer than 5% of patients are alive 5 years from the initial diagnosis
- Surgical resection is possible in about 40% of cases; residual tumor is frequent at the resection margins
- Post operative mortality of 20% due to fistulas, abscesses, and respiratory complications
- < 20% of patients who survive total esophagectomy are alive at 5 years
- Radiation and chemotherapy
- Single agent chemotherapy: decrease in tumor size in 15-25%
- Combinations with cisplatin: reduction in 30-60%
- Preoperative chemotherapy and radiation followed by surgery appears to prolong survival
- For incurable, surgically unresectable patients:
- Endoscopic dilatation
- Gastrostomy, jejunostomy
- Stent - to bypass the tumor
- Endoscopic fulguration of the tumor using lasers
- Most patients present with advanced disease
PET
- Typically FDG is used
- Assesses metabolic activity
- As opposed to size as used in CT
- Principle: biochemical changes often precede or are more specific than structural changes in the disease process
- Functional imaging modality: delineation of normal anatomic structures can be difficult
- Cannot define depth of invasion
CT versus PET: Rankin, Taylor et al.
- 25 patients with biopsy proven cancer underwent pre-operative staging
- PET was more sensitive in detecting small nodal metastases
- PET was not as sensitive in detecting peri-esophageal and left gastric lymph nodes because of poor spatial resolution and proximity to the tumor
- PET was more sensitive in detecting distant metastases
- Both are effective in detecting the primary tumor
CT and PET for Staging: Kole, Plukker et al
- 26 patients
- Visualization of primary tumor:
- CT: 81% of patients
- PET: 96% of patients
- Neither could reliably assess wall invasion
- Correlation with surgically assessed nodal status:
- Accuracy for determining surgical resection:
- CT: 65%
- PET: 88%
- Together: 92%
- Overall, PET had a higher sensitivity for nodal and distant metastases as well as a higher accuracy for determining resectability
Improvement in Staging with the addition of PET: Block, Patterson et al
- 58 patients
- PET improved the ability to classify patients as resection candidates
- PET identified sites that were accessible for biopsy and unsuspected metastases in 17 patients with unresectable disease
- Altered the course of treatment
- Advantages of PET: images based on tissue metabolism, 3D whole body images, can detect other primary cancers
- Disadvantages: uptake can occur at inflammatory sites, availability and cost
PET and SUVs: Fukunaga, Okazumi et al.
- 48 patients
- 23 patients with SUV >7 had a poor prognosis
- SUV theories
- May represent a growth rate measurement of residual cancer cells
- Recurrent cases with higher preoperative SUVs had shorter latency periods
- May be assessing tumor viability
- SUV can be a useful tool in assessing treatment effects and postoperative follow-up
- SUV
- Correlates with hexokinase activity of the resected specimen
- Can differentiate benign from malignant (cut-off of 2)
- Index for predicting prognosis prior to surgery
PET and Chemotherapeutic Response: Couper, McAteer et al
- 14 patients: imaging performed prior to and following chemotherapy (after 2 or 3 cycles)
- PET was able to detect responses post chemotherapy (range: complete response to 15% increase)
- PET can play a role in patient selection for continued treatment
- Can play a role in monitoring treatment in patients receiving palliative chemotherapy
11 C-Choline PET Imaging
- Methyl 11 C choline
- Choline is a blood constituent that penetrates cell membranes
- In tumors, choline integrates into phospholipids
- 11 C-choline is phosphorylated in tumor cells where it remains: "chemical trap"
- As tumor cells replicate, the biosynthesis of cell membranes is fast
- Therefore, the uptake rate of 11 C-choline in tumors is proportional to the rate of tumor duplication
11 C-choline and FDG: Kobori et al
- 33 patients
- 11 C-choline was more effective in detecting very small mediastinal metastases than FDG and CT
- Minimal size detected: 4mm
- 11 C-choline was more sensitive in detecting small tumors than FDG
- 11 C-choline was less useful in imaging the upper abdomen because it is normally taken up by the liver
- With 11 C-choline and FDG, 85% of metastatic lymph nodes were detected in the upper abdomen and mediastinum
Role of PET
- Determining benign from malignant lesions
- Demonstrating primary tumor
- Limited use in loco-regional lymph node evaluation
- Detecting distant metastases and other primaries
- Determine surgical resection candidates
- Determine treatment response, i.e., to chemotherapy
References
Block M, Patterson A, et al. Improvement in staging of esophageal cancer with the addition of positron emission tomography. Ann Thorac Surg 1997; 64:770-777.
Fukunaga T, Okazumi S, et al. Evaluation of esophageal cancers using fluorine-18-fluorodeoxyglucose PET. J Nucl Med 1998; 39:1002-1007.
Kole AC, Plukker JT, et al. Positron emission tomography for staging of oesophageal and gastroesophageal malignancy. British Journal of Cancer 1998; 78(4):521-527.
Kobori O, Kirihara Y, et al. Positron emission tomography of esophageal carinoma using 11C-choline and 18F-fluorodeoxyglucose. Caner 1999; 86:1638-1648.
Luketich J, Schauer P, et al. Role of positron emission tomography in staging of esophageal cancer. Ann Thorac Surg 1997; 64:765-769.
McAteer D, Wallis F, et al. Evaluation of 18F-FDG positron emission tomography in gastric and oesophageal carcinoma. The British Journal of Radiology, 72 (1999), 525-529.
Rankin SC, Taylor H, et al. Computed tomography and positron emission tomography in the preoperative staging of oesophageal carcinoma. Clinical Radiology (1998) 53, 659-665.
Click here to go
to Joint Program in Nuclear Medicine home page and Copyright
notice.
J. Anthony Parker, MD PhD, Tony_Parker@CareGroup.Harvard.edu