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dc.contributor.authorEward, William C.
dc.contributor.authorMito, Jeffrey K.
dc.contributor.authorEward, Cindy A.
dc.contributor.authorCarter, Jessica E.
dc.contributor.authorKirsch, David G.
dc.contributor.authorBrigman, Brian E.
dc.contributor.authorFerrer, Jorge M
dc.date.accessioned2017-01-26T23:55:47Z
dc.date.available2017-01-26T23:55:47Z
dc.date.issued2012-09
dc.identifier.issn0009-921X
dc.identifier.issn1528-1132
dc.identifier.urihttp://hdl.handle.net/1721.1/106648
dc.description.abstractBackground Treatment of soft tissue sarcoma (STS) includes complete tumor excision. However, in some patients, residual sarcoma cells remain in the tumor bed. We previously described a novel hand-held imaging device prototype that uses molecular imaging to detect microscopic residual cancer in mice during surgery. Questions/purposes To test this device in a clinical trial of dogs with naturally occurring sarcomas, we asked: (1) Are any adverse clinical or laboratory effects observed after intravenous administration of the fluorescent probes? (2) Do canine sarcomas exhibit fluorescence after administration of the cathepsin-activated probe? (3) Is the tumor-to-background ratio sufficient to distinguish tumor from tumor bed? And (4) can residual fluorescence be detected in the tumor bed during surgery and does this correlate with a positive margin? Methods We studied nine dogs undergoing treatment for 10 STS or mast cell tumors. Dogs received an intravenous injection of VM249, a fluorescent probe that becomes optically active in the presence of cathepsin proteases. After injection, tumors were removed by wide resection. The tumor bed was imaged using the novel imaging device to search for residual fluorescence. We determined correlations between tissue fluorescence and histopathology, cathepsin protease expression, and development of recurrent disease. Minimum followup was 9 months (mean, 12 months; range, 9–15 months). Results Fluorescence was apparent from all 10 tumors and ranged from 3 × 107 to 1 × 109 counts/millisecond/cm2. During intraoperative imaging, normal skeletal muscle showed no residual fluorescence. Histopathologic assessment of surgical margins correlated with intraoperative imaging in nine of 10 cases; in the other case, there was no residual fluorescence, but tumor was found at the margin on histologic examination. No animals had recurrent disease at 9 to 15 months. Conclusions These initial findings suggest this imaging system might be useful to intraoperatively detect residual tumor after wide resections. Clinical Relevance The ability to assess the tumor bed intraoperatively for residual disease has the potential to improve local control.en_US
dc.publisherSpringer-Verlagen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s11999-012-2560-8en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSpringer-Verlagen_US
dc.titleA Novel Imaging System Permits Real-time in Vivo Tumor Bed Assessment After Resection of Naturally Occurring Sarcomas in Dogsen_US
dc.typeArticleen_US
dc.identifier.citationEward, William C., Jeffrey K. Mito, Cindy A. Eward, Jessica E. Carter, Jorge M. Ferrer, David G. Kirsch, and Brian E. Brigman. “A Novel Imaging System Permits Real-Time in Vivo Tumor Bed Assessment After Resection of Naturally Occurring Sarcomas in Dogs.” Clinical Orthopaedics and Related Research® 471, no. 3 (September 13, 2012): 834–842.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorFerrer, Jorge M
dc.relation.journalClinical Orthopaedics and Related Research®en_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2016-08-18T15:46:18Z
dc.language.rfc3066en
dc.rights.holderThe Association of Bone and Joint Surgeons®
dspace.orderedauthorsEward, William C.; Mito, Jeffrey K.; Eward, Cindy A.; Carter, Jessica E.; Ferrer, Jorge M.; Kirsch, David G.; Brigman, Brian E.en_US
dspace.embargo.termsNen
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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