Selective use of PET scan in the preoperative staging of NSCLC
Introduction
The management of primary lung cancer depends on accurate staging. If disseminated disease is found surgery is generally contraindicated. Chest X-ray and CT scan are the imaging techniques routinely used for the preoperative evaluation of the patients with lung cancer, occasionally supplemented by magnetic resonance imaging (MRI). These examinations rely on size and density rather than the metabolic properties of the lesions. The sensitivity and specificity of these techniques is not ideal [1]. Invasive diagnostic techniques such as fine needle aspiration biopsy are frequently required before surgical therapy if a concomitant lesion is detected on CT scan. Despite thorough investigations, preoperative staging fails to identify metastatic deposits in a significant proportion of the patients who undergo thoracotomy [2].
In recent years, increasing interest has focused on positron emission tomography (PET), which identifies metabolically active foci, for the assessment of patients with lung cancer [3]. PET scan has been used clinically only in the last decade, although the principal mechanism on which it is based is an observation made in 1930 [4]. Warburg observed that cancer cells are characterised by higher glycolytic rate than normal cells. Deoxyglucose is a glucose analogue which is transported into cells by the same carrier proteins for glucose [5]. Deoxyglucose, like glucose, is phosphorylated by hexokinase to deoxyglucose-6-phosphate which does not proceed further in the metabolic pathway and remains metabolically trapped in the cell. Deoxyglucose is radiolabelled with the positron emitter 18-F. 18-F-fluoro-2-deoxy-d-glucose (FDG) is taken up by normal and malignant tissue and the amount of FDG which accumulates in the cell is proportional to the rate of glucose metabolism.
The first oncologic application of PET FDG was in brain tumours [6]. The technique was used not only for diagnosis but also for metabolic characterisation and assessment of prognosis of brain tumours [7]. Since Dahlbom and Hoffman developed a new acquisition and processing method for whole body PET scan [8], investigators have started to use this technique to investigate other tumours 9, 10, 11.
In lung cancer, the value of PET scan has been tested in different clinical conditions including the assessment of solitary pulmonary nodules, staging of primary disease, the detection of persistent or recurrent disease following treatment, and detection of unsuspected distant metastases 12, 13, 14. Early reports suggest that the technique has great potential on imaging and preoperative staging of lung cancer. This study focused on value of PET FDG for the assessment of the concomitant lesions found on CT scan in patients with NSCLC who were candidates for surgical treatment.
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Material and method
Between October 1995 and December 1996, 21 of the patients who were admitted to Department of Thoracic Surgery at the Royal Brompton Hospital for treatment of primary lung cancer were referred for PET FDG scanning for the assessment of concomitant lesions which were detected on preoperative CT scan. There were ten males and 11 females ranging in age from 44 to 79 years (average, 61.4). Tumour site and cell type are illustrated in Table 1. All patients had histologically proven non-small cell
Results
All 18 primary tumours were detected on the PET scan as well as the second primaries in three cases. None of the tumours measured less than 2 cm in diameter. In one case (no. 14), PET scan was undertaken for the assessment of bilateral tiny nodules in both lungs. Abnormal hilar lymph nodes and a tumour in a collapsed lobe that was not shown on CT scan were detected by PET. Except for this finding PET scan did not detect any additional intrapulmonary lesion that had not been found on CT scan.
The
Discussion
The extent of the disease is the most important factor in determining appropriate treatment and expected survival in patients with primary lung cancer. Despite improvement in the imaging techniques and invasive staging procedures, most deaths following definitive therapy are due to local recurrence or disseminated disease [15]. Even though the pattern of metastasis may be different among the histologic types, it is estimated that 30% of the patients who had resection for cure have undetected
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