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Positron emission tomography (PET) has been in existence and continuously developing over the past 20 years. In the last few years steady advances in the technology used for PET and complementary progress in supporting computer equipment have led to the ability to perform whole body imaging with this modality. With this evolution has come an improved capability for the diagnosis, staging, and post-treatment surveillance of malignancies in the thoracic cavity. This report will review the current status of PET imaging for the investigation of thoracic oncology.
PET scan technique
PET imaging involves the use of specialised radiation sensitive cameras which detect specific radioactive isotopes that decay by positron emission. Most of the common molecules involved in organic processes can be labelled with positron emitting isotopes. Atoms of low atomic number such as carbon, oxygen, nitrogen, and fluorine have positron emitting isotopes. Molecules of specific functional import, labelled with positron emitting isotopes, can be injected intravenously into patients and an image of their distribution can be obtained using a PET camera. Although many different tracers can be manufactured and have been utilised to evaluate malignancy, this review will focus on the use of one tracer, 18F-fluorodeoxyglucose (FDG), which is the most widely used for detection of malignancy.
Malignant tumours usually demonstrate rapid cell proliferation with a proportionally increased cellular metabolism. Physiologically, this translates into increased glucose metabolism in malignant cells, a finding first reported in the 1930s.1-3 Comparable enhancements of glucose and FDG uptake in malignant cells have permitted the identification of malignancy using PET imaging.4 A unique feature of FDG as a marker of glucose metabolism is the fact that, after FDG phosphorylation, FDG-6-PO4 does not proceed further in the metabolic pathway but remains trapped within tumour cells, thus becoming a marker of metabolism. This persistence of the tracer in the tumour is essential for successful imaging to be performed.5 The relative uptake of FDG can be used as an indicator of tumour aggressiveness and correlates with tumour growth rates.6
PET imaging provides numerical data by quantitating the number of positron emissions. These data accurately reflect the amount of FDG accumulating in a selected region. The standardised uptake ratio (SUR) is an uptake value normalised for patient body weight and imaging dose that provides a means of comparison of FDG uptake between patients. It is calculated in the following way:
SUR values of >2.5 have been considered indicative of malignancy by some authors while slightly different values are used by others. Still other investigators depend instead on visual interpretation of abnormality—that is, FDG uptake greater than mediastinal uptake—as being abnormal. FDG imaging is performed in the fasting state to minimise competitive inhibition of FDG uptake by glucose. The effect of diabetes and serum hyperglycaemia on the uptake of FDG in primary lung cancers has not been proven to affect the accuracy of the test although there is a concern because elevated serum glucose levels can result in decreased FDG accumulation in tumour.7 Other PET tracers are available that could avoid this problem if using FDG in hyperglycaemic patients is found to result in a reduction of diagnostic accuracy.8 The PET scans are performed 50–60 minutes after intravenous administration of 10.0–20.0 mCi of FDG and are usually completed after an additional hour of tomography.9 Images are generally displayed as axial, coronal, and sagittal views as well as three-dimensional surface projections. Semiquantitative assessment, as described above, of particular lesions is also often performed. Although images can be obtained of localised areas, the same injection will allow whole body images to be obtained. While images of localised areas may only require 15–30 minutes, a whole body image usually requires an hour or more. In the near future whole body images may well be performed in about 30–40 minutes, largely due to new imaging software and faster computers. Development of new kinds of light detection crystals for use in the next generation of PET scanners is also underway and this may allow improved image resolution when compared with today’s systems.
Evaluation of focal lung abnormalities
Focal lung abnormalities such as a defined nodule or a non-specific opacity often need to be evaluated for malignancy. Imaging with chest radiography, computed tomography (CT) or magnetic resonance imaging (MRI) will rarely characterise focal lung abnormalities definitively as benign or malignant since the classic radiographic finding of centralised calcification is only infrequently seen.10 11 Several invasive modalities are available to assist in the diagnosis of these radiographic lesions. Bronchoscopy, including bronchial washings and brushing, has a limited sensitivity of 65% for malignancy and the addition of transbronchial biopsy only increases the sensitivity to 79%.12 13 Bronchoscopy proves most helpful in the more central lesions that are bronchoscopically accessible. Peripheral lesions can also be biopsied percutaneously with the help of CT guidance. Published reports suggest that CT guided transthoracic needle aspiration (TTNA) has a sensitivity and specificity of 94–98% and 91–96%, respectively.14 15
Negative results from transbronchial biopsies and/or transthoracic needle aspirations (TTNA) can not be accepted as true negatives at all times. For example, in one study in which TTNA of discrete pulmonary lesions was evaluated in 181 patients, 40% of the biopsy specimens failed to produce a definitive diagnosis and 40% of this subset subsequently proved to be malignant lesions.16 A definitively negative diagnosis by percutaneous fine needle biopsy could be established in only 16% of the patients with benign conditions in this study. In another report the histological reports were reviewed following diagnostic thoracotomy performed on patients in whom TTNA was considered difficult, inappropriate, or was unsuccessfully attempted. Up to 65% of these nodules were incorrectly characterised prior to surgery, and in 50% of patients found to have cancer, malignancy was not the preoperative diagnosis.17There are also risks to these more aggressive diagnostic manoeuvres. Percutaneous biopsy has an 18–26% risk of pneumothorax and 10–15% of patients with post-procedure pneumothorax require chest tubes.15 18
While the recently popularised technique of thoracoscopic lung biopsy provides a definitive diagnosis, in a recent series over 50% of radiographically indeterminate nodules resected by thoracoscopy were benign.19 Thus, half of this patient population underwent an invasive and potentially avoidable surgical procedure.
An accurate non-invasive test for evaluating indeterminate pulmonary lesions could potentially avoid considerable patient morbidity and potentially reduce lower medical costs by obviating invasive procedures. Recently published data have demonstrated the ability of PET to characterise lung abnormalities and have been particularly encouraging.
After the identification of a pulmonary abnormality by an anatomical study such as a chest radiograph, FDG-PET imaging can be performed to evaluate the metabolic activity of the lesion in an attempt to distinguish a benign from a malignant process. Investigators have used FDG-PET in the assessment of focal pulmonary nodules and other pulmonary opacities. In an early report one centre investigated FDG-PET imaging of solitary pulmonary nodules in 30 patients and found that PET had a sensitivity and a specificity of 95% and 80%, respectively.20 In another report 51 patients with focal opacities that could not be characterised as benign or malignant by chest radiography or CT scanning underwent a PET scan. The sensitivity and specificity of FDG-PET imaging for malignancy were found to be 100% and 89%, respectively.21 When FDG uptake within the focal opacities was analysed a highly statistically significant difference was found between the PET SUR value of malignant and benign lesions (p = 0.0001). Figure 1 shows a case of an indeterminate pulmonary nodule that was correctly characterised as tumour by PET imaging.
Table 1 lists a review of data evaluating the use of PET imaging in pulmonary abnormalities. This list includes the most recent comprehensive reports from the institutions reporting PET assessments of lung abnormalities.22-28 Some investigators have included only solitary pulmonary nodules while others have widened the criteria to include any suspicious opacity. The data show that PET imaging performs equally well in either group with an average sensitivity and specificity of 95% and 88% for the detection of malignancy.
As with most medical tests, PET imaging is not 100% accurate. The data demonstrate that there will be a small proportion of pulmonary opacities that will be metabolically active yet benign, resulting in false positive PET scans (table 2). Some active infectious or inflammatory lesions may have significant uptake of FDG. Tuberculous granulomas, coccidiomycosis, aspergillosis and histoplasmosis were causes of some of the false positive results seen in the studies listed. However, these false positives are the exception. More commonly, chronic or indolent inflammatory processes which incite less intense host reactions and a lower rate of FDG accumulation are imaged. For this reason the specificity of PET in the evaluation of pulmonary opacities remains high.
False negative PET studies may also occur and are seen in three specific settings. The first pitfall occurs in tumours with relatively low metabolic activity. In a recent report four of seven bronchioalveolar tumours did not demonstrate increased FDG accumulation29 and carcinoid tumours have also had low levels of FDG accumulation in the series listed.23 24 All other types of primary lung cancer (with variable differentiation) have increased FDG accumulation. Occasionally, well differentiated adenocarcinomas will have a relatively less marked increase in FDG accumulation, but the SUR is still abnormal.29
Size is another potential limitation for accurately identifying cancer. False negative readings can occur due to the relatively limited resolution (5–8 mm) of present PET tomographs and the effect that this has in detecting small abnormalities. This could play a role when the tumours are physically small or when the histological complement of malignant cells is small relative to the rest of the nodule, as might be seen in an early scar carcinoma. The Prospective Investigation of PET in Lung Nodules study28 has shown a lower sensitivity for malignancy (80%) when the tumours were less that 1.5 cm in size. Although one study found no difference in the accuracy of PET when evaluating nodules 2 cm or less compared with those over 2 cm,27 this has not been universally true. This is an area where future technological advances in PET systems may improve overall accuracy. No studies have been performed to look specifically at the accuracy of PET in very small nodules although, in the studies mentioned, each had a few nodules in the 5–8 mm range that were characterised correctly in approximately half the cases.
The final possible, albeit uncommon, cause for false negative PET studies is hyperglycaemia. Competitive inhibition from high serum glucose levels appears to hinder FDG uptake in some cases. Research has shown that the inhibitory effect is most important with acute hyperglycaemia while a chronically raised glucose level only inhibits tumour uptake of FDG minimally (by about 10%).8 Diabetic control should therefore be optimised and serum glucose values checked prior to PET imaging. If significant hyperglycaemia (>300 mg/dl) is identified, a return appointment at a time when diabetic control is improved is the suggested course of action. In the above series false negative cases from hyperglycaemia were described in only two instances.
Algorithms for using PET imaging in focal lung abnormalities
The optimal algorithm incorporating PET imaging for the evaluation of pulmonary abnormalities has not yet been identified. FDG-PET evaluation of solitary pulmonary nodules could identify metabolically inactive lesions likely to be benign. Patients with such lesions could be followed by sequential imaging studies rather than undergo invasive sampling procedures. One study has compared the use of TTNA and PET in the investigation of indeterminate nodules. The sensitivity and specificities were 100% and 78% for PET and 81% and 100% for TTNA.30 These data suggest that more malignancies may in fact be missed using a traditional TTNA approach than with PET imaging when triaging patients for thoracotomy. Conversely, a PET approach may lead to more unnecessary thoracotomies given the data from this series. One must decide whether a missed cancer diagnosis or an unnecessary thoracotomy represents the greater risk. Also of note is that nine of 33 of the patients in this series (26%) required chest tube placement for pneumothoraces secondary to the TTNA. The costs and benefits of different diagnostic strategies are being evaluated.
Staging lung cancer
Staging of bronchogenic carcinoma is performed using the TNM system which requires accurate evaluation of the primary tumour (T), regional lymph nodes (N), and distant metastasis (M). The following discussion illustrates the role of FDG PET scanning for these three components of staging.
Although tumour size can be estimated on PET imaging, thus allowing classification into T1 (<3 cm) and T2 (>3 cm) lesions, this is accurately determined on CT scanning. Similarly, PET scanning has poor accuracy in determining invasion into adjacent structures such as chest wall, diaphragm, spine, or large vessels—characteristics that determine T3 or T4 status. The identification of pleural metastasis (which constitutes T4 disease) is perhaps the most useful, if highly infrequent, discovery that can be made accurately by PET imaging when dealing with the determination of the T status.
REGIONAL LYMPH NODE DISEASE
PET has greater utility in nodal staging of bronchogenic carcinoma. Table 3 is a list of staging studies examining the accuracy of PET in staging lung cancer.31-38 Staging of the mediastinum can be performed by mediastinoscopy which has a sensitivity of 87–91% for disease.39-41 Staging by anatomical imaging studies such as CT scanning has been attempted but is considered by some to be only complementary to mediastinoscopy due to its poor accuracy. Adenopathy, as defined by CT imaging (>1 cm short axis diameter), is both insensitive and non-specific for malignancy. CT and MRI staging of bronchogenic carcinoma has been reported to have a sensitivity of about 50–60%.42-44 Interestingly, nodes greater than 2 cm have been reported to have a 30–37% chance of being benign,42 45 leading to the non-specificity seen for CT scanning. Figure 2 shows a case of nodal disease identified by PET imaging.
Several studies in the last few years have demonstrated the superiority of PET over CT scanning in the evaluation of nodal stage (table 3). These reports have included relatively small patient groups but the differences between PET imaging and CT scanning were statistically significant. There is minimal variation in the nodal size criteria used for CT scanning. The studies also have some variation in the rigor of nodal sampling, as noted in the number of nodal stations reported. Some of the reports only list the nodal status of individual patients while others detail the number of positive nodes. The study by Steinert and coworkers probably demonstrates the most comprehensive sampling of all of the studies. In table 3 the average sensitivity and specificity of the studies for nodal disease was 88% and 91% for PET imaging and 63% and 76% for CT scanning. This average sensitivity of PET for nodal disease is near that reported for mediastinoscopy. Of note is the lower sensitivity reported by Sasaki and coworkers33 for nodal disease. They used a PET tomograph with lower spatial resolution (14 mm) and may therefore have had difficulty identifying smaller tumour volumes. In fact, all four of the nodal regions that were false negative on PET imaging in their study had positive nodes that were less than 7 mm in size. They did identify some other nodal disease that was 7 mm in size.
A whole body PET image can be obtained to assess metastatic disease status. Table 4 lists three studies that looked at the data provided by PET imaging in assessing distant metastatic disease.37 46 47 In each of the reports at least 10% of the patients were found to have distant metastasis not otherwise detected by routine chest CT scans or additional imaging studies such as bone scans. The results imply that information regarding advisability of tumour resection will be impacted by adding PET data. Not only was unsuspected disease identified on PET thus resulting in “upstaging”, but many false positive findings on CT scanning (including findings outside of the chest such as adrenal nodules) were correctly interpreted as negative by PET imaging. This was illustrated in a study of 99 patients by Valk and coworkers37 in which PET correctly characterised as benign 14 of the 19 false positive findings reported on CT scans. Thus, PET imaging could aid in identifying cancer patients as surgical candidates who might otherwise be considered unresectable. In considering both contributions, the change in management brought about by the PET information can reach very high proportions of study populations as is illustrated by Lewis and coworkers47 where management changes occurred in 41% of patients. Figure 3 is an example of PET scan findings that characterised other imaging abnormalities as benign.
The adrenal glands are commonly a dilemma in the examination of metastatic disease. Benign enlargement of the adrenal glands occurs commonly and is difficult to distinguish from metastatic enlargement of the adrenal glands in patients with lung cancer. Unenhanced CT scans can produce a sensitivity and specificity of about 96% and 73% for metastatic disease to enlarged adrenal glands.48 However, this would commonly necessitate a second adrenal imaging session if CT scanning is performed with contrast medium. MRI of the adrenals using chemical shift imaging can distinguish benign from malignant enlarged adrenal glands with nearly 100% accuracy according to some reports.49 However, this would also require a separate imaging procedure. Furthermore, evaluation by these methods is predicated on anatomical enlargement and normal adrenal glands with tumour may not be detected. It should also be considered that the accuracy of adrenal size characterisation by CT scanning is only good to about ±1 cm.50 Percutaneous biopsy specimens are usually employed to evaluate the possibility of lung cancer metastasis to an enlarged suspicious adrenal gland. However, percutaneous biopsy itself only has an accuracy of about 90% for metastatic disease.48
PET imaging has been shown to have the ability to distinguish benign adrenal enlargement from metastatic disease. In one study of 20 patients by Boland et al 51 PET imaging was able to show a statistically significant difference in lesion metabolism between benign enlarged adrenal glands and those with malignancy. Maurea and colleagues52 found similar results in their study of 15 patients with enlarged adrenal glands. Interestingly, in this study there was no statistically significant difference between the size of the adrenal glands in the benign group compared with the group with malignant enlargement. Recently a study by Erasmus53 showed that, in 27 patients (33 enlarged adrenal glands) with bronchogenic carcinoma, PET imaging correctly identified all adrenal glands with tumour. Eight of 10 benign enlarged adrenal glands had no increase in FDG accumulation and were therefore appropriately identified as being benign by PET. The advantage of using PET imaging in this setting is that, unlike the other imaging modalities, the information about the adrenal glands is obtained in the same imaging session. Also, the technique has the ability to identify tumour in adrenal glands that are normal in size (fig 4). However, the accuracy of PET imaging in assessing normal adrenal glands for metastasis has not been documented.
COST/BENEFIT OF PET STAGING OF LUNG CANCER
Gambhir and coworkers developed a cost/benefit model that demonstrated a significant cost savings by including FDG-PET imaging in the staging of lung cancer.44 They found that a conservative strategy of using chest CT scanning plus PET imaging showed a potential cost savings of $1154 per patient without a loss of life expectancy. This strategy would involve taking biopsy specimens from all positive findings with either CT or PET imaging that might indicate non-resectable malignancy so that 100% of surgical candidates are identified definitively. Chest CT scanning is performed in all patients to insure that proper anatomical information is available to the surgeon. A less conservative strategy in which patients with concordant positive results on CT and PET scanning indicating non-resectability do not undergo biopsy or proceed to thoracotomy would result in a cost saving of $2267 but would miss 1.7% of potentially operable patients. The largest component of the cost savings realised by these approaches results from the prevention of unnecessary surgery and biopsy procedures.
Assessing lung cancer therapy and recurrence
Patients with bronchogenic carcinoma commonly present in an advanced stage and, as such, have a five year survival of 13%.54 An accurate assessment of the impact of chemotherapy and radiation therapy would be of enormous benefit in directing treatment for patients with advanced stages of lung cancer. Historically clinicians have used tumour shrinkage to assess efficacy, but this may not be the best indicator of response to treatment. FDG-PET imaging can identify changes in glucose uptake and may prove to be a better indicator of a favourable response to treatment.
It may be important to differentiate between a decrease in FDG uptake compared with the complete absence of FDG uptake. Some investigators have concluded that a decrease in FDG uptake does not necessarily indicate a good prognosis.55 Rather, it has been suggested that a decrease in FDG uptake may only indicate a partial response due to destruction of cells sensitive to the therapy while other resistant cells continue to be metabolically active. Normalisation of the FDG uptake after treatment, on the other hand, appears to be a good prognostic sign. One study by Hebert and coworkers56demonstrated that negative PET findings after radiation therapy, even in the presence of non-specific radiographic changes, are an indicator of a good response. Hebert noted that all of their patients with negative PET findings were alive at two years after treatment whereas 50% of patients with residual hypermetabolism, albeit reduced, had died within that same two year period. Other investigators have used this logic to justify further treatment of asymptomatic individuals whose PET scans demonstrate residual hypermetabolism after an initial course of therapy. Frank and colleagues treated five such asymptomatic patients in their study based solely on residual hypermetabolism and all were alive at three years.57
Early diagnosis of recurrent lung cancer is another potential use of FDG-PET imaging. Radiological changes such as scarring and necrosis which occur after treatment may obscure the identification of recurrent tumour unless significant volume changes occur over time. The interpretation of recurrence is often not made until the disease progresses to the point of marked enlargement of questionable abnormalities. Unfortunately, a tissue biopsy specimen that is negative for tumour in such situations is suspect due to the inherent difficulty in identifying and accurately sampling the areas of viable tumour hidden in the midst of the scar. A PET evaluation of tumour recurrence can potentially assist in this determination. Patients who have chest radiographic findings suspicious for tumour recurrence can be accurately characterised by FDG-PET imaging as demonstrated in fig 5.
Benign, non-specific pleural thickening is another example of post-treatment changes which may be difficult to differentiate from recurrent disease. Pleural biopsy itself may be relatively unreliable when performed percutaneously. PET imaging will probably differentiate recurrent tumour from radiation inducing benign pleural thickening. Several investigators have examined the use of PET imaging for just these purposes (table 5). Patz and coworkers58demonstrated a very high accuracy of PET imaging in distinguishing recurrent disease from benign treatment effects when patients were scanned 12–24 months after therapy. The report of Inoue and coworkers59 yielded similar results.
There are potential pitfalls for FDG-PET imaging when used for this purpose. Occasionally treatment can induce hypermetabolic inflammatory changes that may make it difficult to differentiate persistent tumour from treatment effect. This is most common when radiation therapy has been used. Chemotherapy does not commonly induce the tissue damage that leads to inflammatory hypermetabolism. The likelihood of seeing moderate levels of hypermetabolism after radiation therapy diminishes as time passes. Scans are likely to be most reliable when a year or more has passed from the last radiation treatment. The most common finding indicative of post-therapy inflammatory hypermetabolism is diffuse, mildly raised FDG accumulation in the soft tissues of radiation port regions.58 A cutoff of 2.5 for the SUR still appears to be accurate in differentiating tumour from benign changes in focal abnormalities identified at the post-treatment setting.
Evolving applications of PET in thoracic oncology
PET imaging may play a role in evaluating other kinds of thoracic cancer. Data are available that have shown the usefulness of PET imaging in identifying breast cancer and staging axillary lymph nodes.60 61 Data from one investigator have shown that PET staging of the axilla detected all of the nodal disease surgically confirmed in a group of 124 patients.62 Figure 6 shows a case of nodal disease accurately characterised by PET in a patient with breast cancer.
Preliminary reports have shown that FDG-PET may help in the evaluation of mediastinal tumours. Thymomas have demonstrated variable FDG uptake which appears to correlate with their invasiveness. Benign cysts and thymic hyperplasia have low FDG accumulation.63 64Moderate levels of FDG accumulation have been seen in myeloma and schwannoma, whereas low uptake has been observed in teratoma and various benign cysts.64 Mediastinal lymphomas have high FDG accumulation and can be accurately identified using PET imaging.65 Increased FDG uptake in lymphomas correlates with high histological grade of malignancy and a high proliferation rate.66 There are also data to indicate the ability of PET imaging to stage lymphoma with improved accuracy over CT scanning.65 Others have shown that FDG-PET imaging may have greater sensitivity than gallium in evaluating lymphomas.67
There has been some work done in the evaluation of chest wall sarcomas. FDG accumulation correlates with sarcoma grade and, although high grade lesions can be distinguished from benign lesions, low grade neoplasms may appear similar to benign lesions.68-70 A known high grade lesion may therefore be amenable to PET imaging for determining stage or evaluating disease recurrence after treatment.
Although a great deal of data has been accumulated regarding PET evaluation of solitary pulmonary masses, little specific information exists on the usefulness of PET in evaluating multiple pulmonary masses. Nevertheless, reports have described the accuracy of FDG-PET as being greater than other imaging modalities in identifying pulmonary metastasis from other malignancies such as colon cancer71or melanoma.72 73
Evaluation of oesophageal malignancy
Oesophageal cancer will be diagnosed in 11300 people in the USA this year and is considered to be one of the most important cancers of developing countries.74 The incidence of the disease is much higher in Asia, Northern France, and some other scattered regions in which oesophageal cancer is endemic. The overall survival rate is 10% or less at five years because of the advanced stage of disease at the time of presentation.
Early stage oesophageal cancer is often asymptomatic and detection is uncommon prior to advanced stages of tumour spread. Unfortunately, current staging techniques are still inaccurate and understage oesophageal malignancies in a significant portion of patients. More precise staging will be critical for treatment of patients with oesophageal cancer and could allow truly “early stage” patients to undergo immediate surgery while advanced stage patients would be referred for the promising multimodality treatment protocols. Current routine staging studies are not acceptably sensitive.
Endoscopic evaluation is an accepted method of evaluating oesophageal cancer and has the advantages of allowing both direct visualisation and tissue sampling. Although the addition of endoscopic ultrasound has added an important tool for the detection of paraoesophageal lymph nodes, the accuracy of this technique is operator dependent and somewhat controversial. It certainly has no role in the detection of distant disease.
Non-invasive imaging with chest radiography and chest and abdomen CT scanning is performed to identify lesions in the liver, adrenal glands or lung but is notoriously inaccurate in identifying non-bulky lymphadenopathy and has no hope of spotting lesions that are more distant. New data are emerging regarding the use of PET in staging oesophageal cancer. Several centres have reported substantial advantages to staging oesophageal cancer with PET imaging when compared with conventional techniques. In one study PET had a sensitivity for predicting local nodal disease of 76% (22/29) compared with 45% (13/29) for CT scanning75 in patients who underwent curative surgery. In the same study, in another seven patients who did not undergo surgery PET detected distant metastases in five patients who had no metastatic disease identified on CT scanning. Inappropriate surgery in these patients was thereby prevented by the PET findings. Another patient had an unsuspected concomitant lung primary discovered with PET imaging. In another study of 35 patients with potentially resectable oesophageal cancer, as determined by CT scanning, distant metastatic disease was identified by PET imaging in 20%. The accuracy of PET for determining distant metastatic disease in this group was 91%.76 Figure 7 illustrates patients with oesophageal cancer in whom distant disease was identified only with PET scans and subsequently confirmed surgically, thus averting surgical resection. The use of PET imaging in patients with oesophageal cancer could lead to more accurate staging and allow more accurate stratification of patients into surgical and multimodality protocols. Further work will need to be done to see if the introduction of PET imaging into the staging work up of these patients will lead to any survival benefit. Ultimately any substantial improvement in the survival rates will depend upon successful treatment regimens. In the short term some operative risk may be avoided in patients with previously undocumented metastatic disease.
Continuing advances in PET imaging have resulted in an improved ability to evaluate thoracic malignancies. Published reports demonstrate that PET provides accurate, non-invasive detection and staging of thoracic malignancy. Preliminary studies suggest that PET may also be able to assess the therapeutic response accurately. The studies investigating PET have been relatively small but have shown statistically significant advantages over conventional non-invasive techniques in accuracy and possibly even cost/benefit performance in thoracic malignancies.