4.1 Article

Fluorodeoxyglucose positron emission tomography in leiomyosarcoma: imaging characteristics

期刊

NUCLEAR MEDICINE COMMUNICATIONS
卷 30, 期 7, 页码 546-549

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MNM.0b013e32832bcaec

关键词

fluorodeoxyglucose positron emission tomography; leiomyosarcoma; maximum tumor standard uptake value; sarcoma

资金

  1. NIH/NCI [RO1 CA 65537]

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Objective Leiomyosarcoma, a malignant neoplasm of smooth muscle, accounts for 7% of the sarcomas. Patients with leiomyosarcoma tumors have an average survival of 5 years. These tumors, which are derived from mesenchymal tissues, are difficult to diagnose, and treatment options remain controversial. The relatively rare incidence of this soft tissue sarcoma subtype has limited the number of patients available for studies and research. This study examines whether the imaging characteristics of positron emission tomography (PET) with radiolabeled fluorodeoxyglucose (FDG) provide a reliable, noninvasive means to predict tumor behavior in patients with leiomyosarcomas. Methods [F-18]-FDG-PET was performed on the tumors of participating patients before the neoadjuvant chemotherapy or resection, and a maximum tumor standard uptake value (SUVmax) was calculated. Results The SUVmax was correlated with tumor grade (P = 0.001) and tumor size as greatest dimension (P = 0.004). Analysis of these data indicated the potential effectiveness of FDG-PET imaging in predicting tumor grade. Conclusion In leiomyosarcoma, the SUVmax from FDG-PET is a likely predictor of tumor behavior. The results of this study suggest that a large (by greatest dimension) intermediate grade tumor is expected to have the same predicted outcome as a high-grade tumor and should be treated in the same manner, as they share the same prognosis by definition of tumor grade. Improvements made in the clinical treatment of leiomyosarcomas by use of FDG-PET imaging data may lead to an increase in patient survival. Nucl Med Commun 30:546-549 (C) 2009 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.

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