Screening for distant metastases in patients with head and neck cancer: Is there a role for 18FDG-PET?
Introduction
The detection of distant metastases at the time of initial evaluation changes the prognosis and influences the selection of treatment modality in patients with head and neck squamous cell carcinoma (HNSCC). Distant metastases usually occur late in the course of the disease. The lungs, bone and liver are the most frequent sites of distant metastases. The prevalence of distant metastases in HNSCC at autopsy (37–57%) is much higher than in clinical studies (4–26%).1, 2, 3, 4 Distant metastases that appear during follow-up in patients who achieved locoregional control must have arisen from subclinical distant spread already present at the time of treatment. Patients with distant metastases are generally not considered curable and almost always receive only palliative treatment.5
Because of the relatively low incidence of distant metastases at presentation, only patients with risk factors should undergo evaluation for distant metastases. In a previous study6 in the 1990s, we evaluated the value of screening for distant metastases retrospectively in 101 patients with advanced stage HNSCC, scheduled for major surgery, who underwent chest radiographs, chest computer tomography (CT), ultrasound or CT scan of the liver and bone scintigraphy. We identified several risk factors for development of distant metastases and found that chest CT was the single most important technique that was available for screening for distant metastases in HNSCC patients at that time. Besides lung metastases, chest CT can also detect primary lung cancer, mediastinal lymph node metastases, bone metastases in spine and ribs, and can be extended to the liver. Therefore, we continued performing chest CT only in screening for distant metastases in HNSCC patients with risk factors: three or more cervical metastases, bilateral or low-jugular (level IV) cervical metastases, cervical metastases larger than 6 cm, recurrence or second primary tumours.
Despite negative screening and locoregional tumour control some patients develop distant metastases. These distant metastases must have been present at diagnostic work-up, but were apparently below the detection limit of screening tests. If distant spread occurs early after major surgery with curative intent these patients probably underwent inappropriate extensive treatment.
Thus a more sensitive diagnostic technique which preferably examines the whole body is needed. Positron emission tomography (PET) using the radiolabeled glucose analog 18-fluoro-2-deoxy-glucose (18FDG) offers a functional imaging approach for the entire body. 18FDG-PET is shown to be able to detect various types of tumours, among which HNSCC.7 However, false positive results can occur and confirmation of PET findings can be problematic. The current study evaluates the value of 18FDG-PET in screening for distant metastases in HNSCC patients. The 18FDG-PET results are compared with the results of chest CT in HNSCC patients with risk factors for distant metastases.
Section snippets
Materials and methods
Between May 1998 and August 1999, 34 consecutive HNSCC patients (12 females and 22 males, mean age 59 years, range 25–85), who had risk factors for developing distant metastases underwent screening for distant metastases and synchronous second primary tumours. Primary tumour sites included oral cavity, oropharynx, hypopharynx, larynx, nasopharynx and lymph node metastases of unknown primary tumour. Some patients were already known with secondary primary HNSCC at the time of screening. These
Results
Preoperatively, four patients (12%) were identified with distant metastases (n = 1) or second primary tumours (n = 3). CT and 18FDG-PET detected lung metastases in one patient and primary lung cancer in another (Fig. 1). 18FDG-PET also detected a hepatocellular carcinoma, which was confirmed by ultrasound guided fine needle aspiration cytology and a coloncarcinoma, which was confirmed histopathologically. These four patients were treated palliatively. Increased uptake sites in lung (n = 2), liver (n =
Discussion
In patients at risk for disseminated head and neck cancer, the added value of PET to chest CT in detecting distant metastases and second primary tumours was 6% (95%CI 2–19%). In this relatively small study, this added value consisted of the identification of second primary tumours outside of the thorax. The observer agreement of PET readings was substantial.
Our data stipulate that abnormal 18FDG-PET findings should be confirmed otherwise, and that patients with unconfirmed foci should be given
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