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[F-18]-fluorodeoxy-D-glucose–positron emission tomography response is associated with outcome for extremity osteosarcoma in children and young adults

dc.contributor.authorHawkins, Douglas S.en_US
dc.contributor.authorConrad, Ernest U.en_US
dc.contributor.authorButrynski, James E.en_US
dc.contributor.authorSchuetze, Scott M.en_US
dc.contributor.authorEary, Janet F.en_US
dc.date.accessioned2009-08-12T15:36:37Z
dc.date.available2010-10-05T18:27:30Zen_US
dc.date.issued2009-08-01en_US
dc.identifier.citationHawkins, Douglas S.; Conrad, Ernest U.; Butrynski, James E.; Schuetze, Scott M.; Eary, Janet F. (2009). "[F-18]-fluorodeoxy-D-glucose–positron emission tomography response is associated with outcome for extremity osteosarcoma in children and young adults." Cancer 115(15): 3519-3525. <http://hdl.handle.net/2027.42/63561>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/63561
dc.description.abstractBACKGROUND: Response to neoadjuvant chemotherapy is 1 of the most powerful prognostic factors for extremity osteosarcoma. [F-18]-fluorodeoxy-D-glucose–positron emission tomography (FDG-PET) is a noninvasive imaging modality that is used to predict histopathologic response. To determine the prognostic value of FDG-PET response for progression-free survival (PFS) in osteosarcoma, the authors of this report reviewed the University of Washington Medical Center experience. METHODS: Forty patients with extremity osteosarcoma were evaluated by FDG-PET. All patients received neoadjuvant and adjuvant chemotherapy. FDG-PET standard uptake values (SUVs) before neoadjuvant chemotherapy (SUV1) and after neoadjuvant chemotherapy (SUV2) were analyzed and correlated with histopathologic response. RESULTS: The median SUV1 was 6.8 (range, 3.0-24.1), the median SUV2 was 2.3 (range, 1.2-12.8), and the median SUV2 to SUV1 ratio (SUV2:1), was 0.36 (range, 0.12-1.10). A good FDG-PET response was defined as anSUV2 <2.5 or an SUV2:1 ≤0.5. FDG-PET responses according to SUV2 and SUV2:1 were concordant with histologic response in 58% and 68% of patients, respectively. SUV2 was associated with outcome (4-year PFS, 73% for SUV2 <2.5 vs 39% for SUV2 ≥2.5; P = .021). Both the initial disease stage and the histologic response were associated with outcome. CONCLUSIONS: FDG-PET imaging of extremity osteosarcoma was correlated only partially with a histologic response to neoadjuvant chemotherapy. An SUV2 <2.5 was associated with improved PFS. Future prospective studies are warranted to determine whether FDG-PET imaging may be used as a predictor of outcome independent of initial disease stage. Cancer 2009. © 2009 American Cancer Society.en_US
dc.format.extent166747 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.title[F-18]-fluorodeoxy-D-glucose–positron emission tomography response is associated with outcome for extremity osteosarcoma in children and young adultsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Medical Oncology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Pediatrics, Seattle Children's Hospital, Seattle, Washington ; Fax: (206) 987-3946 ; Seattle Children's Hospital, 4800 Sandpoint Way, Mailstop: B-6553, Seattle, WA 98105-0371en_US
dc.contributor.affiliationotherDepartments of Orthopedics and Radiology, University of Washington Medical Center, Seattle, Washingtonen_US
dc.contributor.affiliationotherDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusettsen_US
dc.contributor.affiliationotherDepartments of Orthopedics and Radiology, University of Washington Medical Center, Seattle, Washingtonen_US
dc.identifier.pmid19517457en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/63561/1/24421_ftp.pdf
dc.identifier.doi10.1002/cncr.24421en_US
dc.identifier.sourceCanceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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