4.6 Article

Conventional Cancer Screening versus PET/CT in Dermatomyositis/Polymyositis

Journal

AMERICAN JOURNAL OF MEDICINE
Volume 123, Issue 6, Pages 558-562

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjmed.2009.11.012

Keywords

Cancer; Dermatomyositis; Paraneoplastic; Polymyositis; Positron emission tomography/computed tomography; Screening

Funding

  1. Spanish Ministry of Health and Consumer Affairs [FIS/2008 PI 08-0450]

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OBJECTIVE: To determine the value of whole-body [F-18] fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) for diagnosing occult malignant disease in patients with myositis compared with broad conventional cancer screening. METHODS: We prospectively studied 55 consecutive patients with a recent diagnosis of myositis in 3 teaching hospitals over a 3-year period by whole-body FDG-PET/CT and compared the results with those of conventional cancer screening, which included thoracoabdominal CT, mammography, gynecologic examination, ultrasonography, and tumor marker analysis. Comparisons were made using predictive values and their 95% confidence intervals. RESULTS: A total of 9 of 55 patients were diagnosed with paraneoplastic myositis. FDG uptake was positive in 7 patients (1 false-positive), negative in 44 patients (3 false-negative), and inconclusive in 4 patients. Positive and negative predictive values of FDG-PET/CT for the diagnosis of cancer were 85.7% and 93.8%, respectively. Conventional screening was cancer-positive in 9 patients (2 false-positive) and negative in the remaining 46 patients (2 false-negative). Positive and negative predictive values were 77.8% and 95.7%, respectively. The overall predictive value of broad conventional screening was the same as that of FDG-PET/CT (92.7 vs 92.7). CONCLUSION: The performance of FDG-PET/CT, a single imaging study, for diagnosing occult malignant disease in patients with myositis was comparable to that of broad conventional screening, which includes multiple tests. (C) 2010 Elsevier Inc. All rights reserved. The American Journal of Medicine (2010) 123, 558-562

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