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Ann Thorac Surg 2004;78:1903-1909
© 2004 The Society of Thoracic Surgeons


Original Article: General Thoracic

Repeat FDG-PET After Neoadjuvant Therapy is a Predictor of Pathologic Response in Patients With Non-Small Cell Lung Cancer

Robert J. Cerfolio, MDa,*, Ayesha S. Bryant, MSPHb, Thomas S. Winokur, MDc, Buddhiwardhan Ohja, MD, MPHd, Alfred A. Bartolucci, PhDe

a Department of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA and Division of Cardiothoracic Surgery, Department of Surgery, Birmingham Veterans Administration Hospital, Birmingham, Alabama; USA
b Department of Epidemiology, UAB School of Public Health, Birmingham, Alabama, USA
c Department of Clinical Pathology, UAB School of Public Health, Birmingham, Alabama, USA
d Department of Nuclear Medicine, UAB School of Public Health, Birmingham, Alabama, USA
e Department of Biostatistics, UAB School of Public Health, Birmingham, Alabama, USA

Accepted for publication June 2, 2004.

* Address reprint requests to Dr Cerfolio, Division of Cardiothoracic Surgery, University of Alabama at Birmingham, 1900 University Blvd, THT 712, Birmingham, AL35294 (E-mail: robert.cerfolio{at}ccc.uab.edu).

BACKGROUND: Repeat positron emission tomography (PET) with 18F-fluorodeoxyglucose (FDG) and chest computed tomography (CT) are used to assess the effectiveness of chemoradiotherapy in patients with non-small cell lung cancer (NSCLC); however, the change in the standardized uptake values (SUV) has not been correlated with the pathologic change of the primary tumor.

METHODS: This is a retrospective cohort study of a prospective database of 56 patients who had NSCLC, FDG-PET, and chest CT scans both before and after neoadjuvant therapy, followed by complete resection of their cancer. Maximum SUVs (maxSUV) and tumor size were measured, and the percentage of change was compared with the percentage of nonviable tumor cells. The primary objective was to measure the degree of correlation between these values.

RESULTS: The change in the maxSUV has a near linear relationship to the percent of nonviable tumor cells in the resected tumors. FDG-PET's maxSUV is better correlated to pathology than the change in size on CT scan (r2 = 0.75, r2 = 0.03, p < 0.001). When the maxSUV decreased by 80% or more, a complete pathologic response could be predicted with a sensitivity of 90%, specificity of 100%, and accuracy of 96%.

CONCLUSIONS: The change in maxSUV on FDG-PET scan after neoadjuvant therapy holds a near linear relationship with pathologic response. It is a more accurate predictor than the change of size on CT scan. When the maxSUV decreases by 80% or more it is likely that the patient is a complete responder irrespective of cell type, neoadjuvant treatment, or the final absolute maxSUV. These findings may help guide treatment strategies.


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