Vo, Kieuhoa T., Matthay, Katherine K., Neuhaus, John, London, Wendy B., Hero, Barbara, Ambros, Peter F., Nakagawara, Akira, Miniati, Doug, Wheeler, Kate, Pearson, Andrew D. J., Cohn, Susan L. and DuBois, Steven G. (2014). Clinical, Biologic, and Prognostic Differences on the Basis of Primary Tumor Site in Neuroblastoma: A Report From the International Neuroblastoma Risk Group Project. J. Clin. Oncol., 32 (28). S. 3169 - 3178. ALEXANDRIA: AMER SOC CLINICAL ONCOLOGY. ISSN 1527-7755

Full text not available from this repository.

Abstract

Purpose Neuroblastoma (NB) is a heterogeneous tumor arising from sympathetic tissues. The impact of primary tumor site in influencing the heterogeneity of NB remains unclear. Patients and Methods Children younger than age 21 years diagnosed with NB or ganglioneuroblastoma between 1990 and 2002 and with known primary site were identified from the International Neuroblastoma Risk Group database. Data were compared between sites with respect to clinical and biologic features, as well as event-free survival (EFS) and overall survival (OS). Results Among 8,369 children, 47% had adrenal tumors. All evaluated clinical and biologic variables differed statistically between primary sites. The features that were > 10% discrepant between sites were stage 4 disease, MYCN amplification, elevated ferritin, elevated lactate dehydrogenase, and segmental chromosomal aberrations, all of which were more frequent in adrenal versus nonadrenal tumors (P < .001). Adrenal tumors were more likely than nonadrenal tumors (adjusted odds ratio, 2.09; 95% CI, 1.67 to 2.63; P < .001) and thoracic tumors were less likely than nonthoracic tumors (adjusted odds ratio, 0.20; 95% CI, 0.11 to 0.39; P < .001) to have MYCN amplification after controlling for age, stage, and histologic grade. EFS and OS differed significantly according to the primary site (P < .001 for both comparisons). After controlling for age, MYCN status, and stage, patients with adrenal tumors had higher risk for events (hazard ratio, 1.13 compared with nonadrenal tumors; 95% CI, 1.03 to 1.23; P = .008), and patients with thoracic tumors had lower risk for events (HR, 0.79 compared with nonthoracic; 95% CI, 0.67 to 0.92; P = .003). Conclusion Clinical and biologic features show important differences by NB primary site, with adrenal and thoracic sites associated with inferior and superior survival, respectively. Future studies will need to investigate the biologic origin of these differences. (C) 2014 by American Society of Clinical Oncology

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Vo, Kieuhoa T.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Matthay, Katherine K.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Neuhaus, JohnUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
London, Wendy B.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hero, BarbaraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Ambros, Peter F.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nakagawara, AkiraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Miniati, DougUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wheeler, KateUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Pearson, Andrew D. J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Cohn, Susan L.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
DuBois, Steven G.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-428122
DOI: 10.1200/JCO.2014.56.1621
Journal or Publication Title: J. Clin. Oncol.
Volume: 32
Number: 28
Page Range: S. 3169 - 3178
Date: 2014
Publisher: AMER SOC CLINICAL ONCOLOGY
Place of Publication: ALEXANDRIA
ISSN: 1527-7755
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
PEDIATRIC-ONCOLOGY-GROUP; THORACIC NEUROBLASTOMA; CERVICAL NEUROBLASTOMA; PELVIC NEUROBLASTOMA; NEURO-BLASTOMA; EXPERIENCE; RECOMMENDATIONS; CLASSIFICATION; TERMINOLOGY; MORBIDITYMultiple languages
OncologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/42812

Downloads

Downloads per month over past year

Altmetric

Export

Actions (login required)

View Item View Item