Show simple item record

Comparison of 123 I-metaiodobenzylguanidine (MIBG) and 131 I-MIBG semi-quantitative scores in predicting survival in patients with stage 4 neuroblastoma: A report from the Children's Oncology Group

dc.contributor.authorNaranjo, Arleneen_US
dc.contributor.authorParisi, Marguerite T.en_US
dc.contributor.authorShulkin, Barry L.en_US
dc.contributor.authorLondon, Wendy B.en_US
dc.contributor.authorMatthay, Katherine K.en_US
dc.contributor.authorKreissman, Susan G.en_US
dc.contributor.authorYanik, Gregory A.en_US
dc.date.accessioned2011-05-06T15:38:36Z
dc.date.available2012-09-04T15:27:07Zen_US
dc.date.issued2011-07-01en_US
dc.identifier.citationNaranjo, Arlene; Parisi, Marguerite T.; Shulkin, Barry L.; London, Wendy B.; Matthay, Katherine K.; Kreissman, Susan G.; Yanik, Gregory A. (2011). "Comparison of 123 I-metaiodobenzylguanidine (MIBG) and 131 I-MIBG semi-quantitative scores in predicting survival in patients with stage 4 neuroblastoma: A report from the Children's Oncology Group." Pediatric Blood & Cancer 56(7): 1041-1045. <http://hdl.handle.net/2027.42/83739>en_US
dc.identifier.issn1545-5009en_US
dc.identifier.issn1545-5017en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/83739
dc.description.abstractBackground 123 I-metaiodobenzylguanidine (MIBG) scans are preferable to 131 I-MIBG for neuroblastoma imaging as they deliver less patient radiation yet have greater sensitivity in disease detection. Both 123 I-MIBG and 131 I-MIBG scans were used for disease assessments of neuroblastoma patients enrolled on Children's Oncology Group (COG) high-risk study A3973. The hypothesis was that 123 I-MIBG and 131 I-MIBG scans were sufficiently similar for clinical purposes in terms of ability to predict survival. Procedure Patients enrolled on COG A3973 with stage 4 disease who completed 123 I-MIBG or 131 I-MIBG scans at diagnosis, post-induction, post-transplant, or post-biotherapy were analyzed. The performance of the Curie score for each MIBG scan type in predicting survival was evaluated. At each time point, survival curves for 123 I-MIBG versus 131 I-MIBG were compared using the log-rank test. Results Of the 413 patients on A3973 with at least one MIBG scan, 350 were stage 4. The 5-year event-free survival (EFS) and overall survival (OS) rates were 33.4 ± 3.6% and 45.6 ± 4.0% (N = 350). At post-induction, EFS ( P  = 0.3501) and OS ( P  = 0.5337) for 123 I-MIBG versus 131 I-MIBG were not significantly different. Similarly, comparisons at the three other time points were non-significant. Conclusions We found no evidence of a statistically significant difference in outcome by type of scan. For future survival analyses of MIBG Curie scores, 123 I-MIBG and 131 I-MIBG results may be combined and analyzed overall, without adjustment for scan type. Pediatr Blood Cancer 2011;56:1041–1045. © 2011 Wiley-Liss, Inc.en_US
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.titleComparison of 123 I-metaiodobenzylguanidine (MIBG) and 131 I-MIBG semi-quantitative scores in predicting survival in patients with stage 4 neuroblastoma: A report from the Children's Oncology Groupen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumC.S. Mott Children's Hospital, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherChildren's Oncology Group, University of Florida, Gainesville, Florida ; Children's Oncology Group (COG), University of Florida, 104 N. Main St. Suite 600, Gainesville, FL 32601.en_US
dc.contributor.affiliationotherDepartment of Radiology and Pediatrics, University of Washington School of Medicine and Seattle Children's Hospital, Seattle, Washingtonen_US
dc.contributor.affiliationotherSt. Jude Children's Research Hospital Memphis, Memphis, Tennesseeen_US
dc.contributor.affiliationotherChildren's Oncology Group, Children's Hospital Boston/Dana-Farber Cancer Institute, Boston, Massachusettsen_US
dc.contributor.affiliationotherDepartment of Pediatrics, University of California San Francisco School of Medicine and UCSF Children's Hospital, San Francisco, Californiaen_US
dc.contributor.affiliationotherDuke University Medical Center, Durham, North Carolinaen_US
dc.identifier.pmid21328522en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/83739/1/22991_ftp.pdf
dc.identifier.doi10.1002/pbc.22991en_US
dc.identifier.sourcePediatric Blood & Canceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.