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Courses of Malignant Pheochromocytoma

dc.contributor.authorSisson, James C.en_US
dc.contributor.authorShulkin, Barry L.en_US
dc.contributor.authorEsfandiari, Nazanene H.en_US
dc.date.accessioned2010-06-01T20:27:14Z
dc.date.available2010-06-01T20:27:14Z
dc.date.issued2006-08en_US
dc.identifier.citationSISSON, JAMES C . ; SHULKIN, BARRY L . ; ESFANDIARI, NAZANENE H . (2006). "Courses of Malignant Pheochromocytoma." Annals of the New York Academy of Sciences 1073(1 Pheochromocytoma: First International Symposium ): 505-511. <http://hdl.handle.net/2027.42/73567>en_US
dc.identifier.issn0077-8923en_US
dc.identifier.issn1749-6632en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/73567
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=17102118&dopt=citationen_US
dc.description.abstractSurvival of patients with metastatic pheochromocytoma that have exceeded 30 years without therapy to reduce tumors have been reported. We reviewed the records of 38 patients with malignant pheochromocytoma who had received 131 I-metaiodiobenzylguanidine ( 131 I-MIBG) treatments between 1981 and 1996 to evaluate longevity. Survival from diagnosis to last follow-up exceeded 5 years in 21 of 38 (55%) and ≥10 years in 50%. In 17 of 21, the interval from diagnosis to 131 I-MIBG therapy was greater than 5 years. Survival following 131 I-MIBG was ≥5 years in 12 of 17 and ≥10 years in 7 of 17 patients despite continued evidence of excessive circulating catecholamines. Objective responses to 131 I-MIBG therapy were seen in about 30% and were usually of a few years, duration, but one individual exhibited marked reductions in volume and function of tumors that have persisted for 21 years. No feature, including a remission of >5 years following surgical excision, was found to predict prolonged survival. In summary, many patients with malignant pheochromocytoma will follow a course extending over many years. The role of 131 I-MIBG therapy in longevity is uncertain, but this radiopharmaceutical reduces evidence of tumors in some patients. Criteria for selecting patients who will benefit from treatment remain to be determined.en_US
dc.format.extent148973 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Incen_US
dc.rights2006 New York Academy of Sciencesen_US
dc.subject.otherMalignant Pheochromocytomaen_US
dc.subject.otherMetaiodobenzylguanidineen_US
dc.subject.otherPatient Longevityen_US
dc.subject.otherLong-term Survivalen_US
dc.titleCourses of Malignant Pheochromocytomaen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelScience (General)en_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDivision of Endocrinology and Metabolism, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationotherDivision of Nuclear Medicine, Department of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USAen_US
dc.identifier.pmid17102118en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/73567/1/annals.1353.053.pdf
dc.identifier.doi10.1196/annals.1353.053en_US
dc.identifier.sourceAnnals of the New York Academy of Sciencesen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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