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Preliminary results from intensity-based CT-SPECT fusion in I-131 anti-B1 monoclonal-antibody therapy of lymphoma Presented in part at the Sixth Conference on Radioimmunodetection and Radioimmunotherapy of Cancer, Princeton, New Jersey, October 10-12, 1996.

dc.contributor.authorKoral, Kenneth F.en_US
dc.contributor.authorLin, Shuhongen_US
dc.contributor.authorFessler, Jeffrey A.en_US
dc.contributor.authorKaminski, Mark S.en_US
dc.contributor.authorWahl, Richard L.en_US
dc.date.accessioned2006-04-19T13:30:07Z
dc.date.available2006-04-19T13:30:07Z
dc.date.issued1997-12-15en_US
dc.identifier.citationKoral, Kenneth F.; Lin, Shuhong; Fessler, Jeffrey A.; Kaminski, Mark S.; Wahl, Richard L. (1997)."Preliminary results from intensity-based CT-SPECT fusion in I-131 anti-B1 monoclonal-antibody therapy of lymphoma Presented in part at the Sixth Conference on Radioimmunodetection and Radioimmunotherapy of Cancer, Princeton, New Jersey, October 10-12, 1996. ." Cancer 80(S12): 2538-2544. <http://hdl.handle.net/2027.42/34346>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34346
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9406707&dopt=citationen_US
dc.description.abstractBACKGROUND In treatment of non-Hodgkin's lymphoma patients with predose-plus-I-131-labeled anti-B1 (anti-CD20) monoclonal antibody, an intratherapy single photon emission computed tomography (SPECT) image is an important part of research estimates of tumor dosimetry. For that imaging, a computed tomography (CT)-SPECT fusion is used both to obtain an attenuation map for the space-alternating generalized expectation maximization reconstruction and to provide CT-based volumes of interest (VoI) to determine activity in tumors and organs. Fusion based on external, skin-surface markers has been used but may not correctly superimpose internal structures. METHODS A new algorithm, developed and implemented in the Department of Radiology, University of Michigan, and based on the mutual information of gray-scale values, was investigated. Results from four anti-B1 therapy patients are presented. RESULTS In one patient, the new intensity-based fusion provided total reconstructed counts for kidneys that were higher than those produced by marker-based fusion; therefore, the VoI was probably located more accurately. In a second patient, after an acquisition that did not include any skin markers, the new algorithm produced counts/pixel that were similar for four of five tumors consistent with what is expected from an ideal therapy combined with accurate count density estimates. The fifth tumor was quite small and will have its final activity estimate moved toward consistency with the others after a recovery coefficient multiplication. For four tumors in two patients, direct comparison of the two algorithms yielded count totals that were different by no more than 7.2%. CONCLUSIONS The use of CT-SPECT fusion and subsequent transfer of tumor VoI originally drawn in high-resolution CT space offers potential advantages for quantifying tumor uptake of radioactivity. A new, mutual-information-based fusion algorithm is usable without skin markers. Results indicate that the new fusion algorithm gives equal tumor count values within 7.2% compared with fusion based on external markers. It increases estimates of kidney activity by an average of 6.4%. Cancer 1997; 80:2538-44. © 1997 American Cancer Society.en_US
dc.format.extent557373 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titlePreliminary results from intensity-based CT-SPECT fusion in I-131 anti-B1 monoclonal-antibody therapy of lymphoma Presented in part at the Sixth Conference on Radioimmunodetection and Radioimmunotherapy of Cancer, Princeton, New Jersey, October 10-12, 1996.en_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 Internal Medicine, University of Michigan, Ann Arbor, Michigan ; Nuclear-Medicine Research Center, 3480 Kresge III, 204 Zina Pitcher Place, University of Michigan Medical Center, Ann Arbor MI 48105-0552en_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michiganen_US
dc.identifier.pmid9406707en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34346/1/28_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1097-0142(19971215)80:12+<2538::AID-CNCR28>3.0.CO;2-Cen_US
dc.identifier.sourceCanceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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