FDG-PET in the prediction of pathologic response after neoadjuvant chemoradiotherapy in locally advanced, resectable esophageal cancer
Purpose: To assess the efficacy of 18Fluorodeoxyglucose-positron emission tomography (FDG-PET) for predicting a pathologic response in locally advanced esophageal cancer after neoadjuvant chemoradiotherapy. Methods and Materials: All enrolled patients were treated with neoadjuvant chemoradiotherapy...
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Veröffentlicht in: | International journal of radiation oncology, biology, physics biology, physics, 2005-11, Vol.63 (4), p.1053-1059 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose: To assess the efficacy of
18Fluorodeoxyglucose-positron emission tomography (FDG-PET) for predicting a pathologic response in locally advanced esophageal cancer after neoadjuvant chemoradiotherapy.
Methods and Materials: All enrolled patients were treated with neoadjuvant chemoradiotherapy followed by esophagectomy and underwent two FDG-PET scans, before and after neoadjuvant chemoradiotherapy. We compared the results of the preoperative FDG-PET scans with the pathologic results.
Results: From July 2001 to July 2004, 32 patients (29 men and 3 women) were enrolled in this study. Pathologic complete response (pCR) in the esophagus was achieved in 21 of 32 patients (66%). The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) in the primary tumors of the preoperative FDG-PET were 27%, 95%, 75%, and 71%, respectively. In regional lymph nodes, these values were 16%, 98%, 36%, and 93%, respectively. The mean standardized uptake value (SUV) of primary tumors was initially 5.6 ± 3.6 and changed to 1.5 ± 1.3 after neoadjuvant chemoradiotherapy (
p < 0.05). If analysis of metabolic response (SUV decrease, ΔSUV) was limited to initially highly metabolic primary tumors (SUV ≥4.0), pathologic response was correlated with metabolic response (
p = 0.006).
Conclusions: This study suggested that the pathologic response of an initially highly metabolic tumor after neoadjuvant chemoradiotherapy could be correlated with the metabolic response, and FDG-PET can provide additional information on tumor response to chemoradiotherapy. |
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ISSN: | 0360-3016 1879-355X |
DOI: | 10.1016/j.ijrobp.2005.03.033 |