Ontology type: schema:ScholarlyArticle Open Access: True
2000-10
AUTHORSV Minard, O Hartmann, M C Peyroulet, J Michon, C Coze, A S Defachelle, O Lejars, Y Perel, C Bergeron, P Boutard, G Leverger, J L Stephan, A Thyss, P Chastagner, G Couillault, C Devalck, P Lutz, F Mechinaud, F Millot, D Plantaz, X Rialland, H Rubie
ABSTRACTTo assess the relevance of MYCN amplification and bone lesions in stage 4 neuroblastoma (NB) in infants aged <1 year, 51 infants with stage 4 NB were enrolled. Three groups of patients were defined according to the type of metastases and the resectability of the primary tumour. Group I comprised 21 infants with radiologically detectable bone lesions, Group II 22 patients with an unresectable primary tumour and Group III eight patients with only metaiodobenzylguanidine (MIBG) skeletal uptake. MYCN oncogene content was assayed in 47/51 tumours and found to be amplified in 17 (37%). The 5-year event-free survival (EFS) rate of these 51 infants was 64.1% (+/- 7.1%). In a univariate analysis, bone lesions, MYCN amplification, urinary vanillylmandelic/homovanillic acid ratio and serum ferritin levels adversely influenced outcome. In the multivariate analysis, radiologically detectable bone lesions were the most powerful unfavourable prognostic indicator: the EFS rate was 27.2% for these infants compared to 90% for infants without bone lesions (P<0.0001). Our data emphasize the poor prognosis of infants affected by stage 4 NB with bone lesions, especially when associated with MYCN amplification. Given the poor results in this group whatever the treatment, new therapeutic approaches need to be investigated in the future. More... »
PAGES973-979
http://scigraph.springernature.com/pub.10.1054/bjoc.2000.1412
DOIhttp://dx.doi.org/10.1054/bjoc.2000.1412
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PUBMEDhttps://www.ncbi.nlm.nih.gov/pubmed/10993641
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