Clinical Prognostic Factors in 1277 Patients with Neuroblastoma: Results of The European Neuroblastoma Study Group 'Survey' 1982-1992
Overview
Affiliations
In 1982 the European Neuroblastoma Study Group (ENSG) established a prospective registry for patients with newly diagnosed neuroblastoma ('The ENSG Survey'). Clinical information was collected primarily to: (a) establish an ENSG database; and (b) investigate prognostic factors in neuroblastoma. This paper summarises the results of the survey. By 1992, 1277 patients with a median age of 26 months (range: 0-289 months), gender ratio of 1.19 M:F had been registered from 30 centres. The median follow-up of survivors is 9.7 years (range: 1-14 years). Overall 5-year survival (S) is 45% (95% CI 42-48%), and event-free survival (EFS) is 43% (95% CI 40-45%). For both survival and EFS the key established prognostic factors, stage and age, are highly significant (P<0.001). In particular, patients under 1 year of age at diagnosis, whatever the disease stage, had a more favourable prognosis than older patients; stage 2 (EFS 93% (95% (CI 85-97) versus 76% (95% CI 67-86), P=0.02), stage 3 (EFS 91% (95% CI 82-96) versus 52% (95% CI 44-60), P<0.001) and stage 4 (EFS 59% (95% CI 48-69) versus 16% (95% CI 13-19), P<0.001). Multivariate analysis established that the anatomical location of the primary tumour (i.e. abdominal versus other sites) and primary tumour volume also conferred a statistically significant difference. In stage 4 disease the 20% of patients without demonstrable bone marrow involvement had a more favourable prognosis than those with infiltrated marrow (EFS 36% (95% CI 13-19) versus 16% (95% CI 29-45), P<0.001). Urine catecholamine metabolite levels (raised versus normal), histology (ganglioneuroblastoma versus neuroblastoma) and gender had no significant effect on outcome after stage and age were accounted for. 5-year survival following first relapse is only 5.6% (95% CI 2.8-8.4). This ENSG Survey provides secure data for future comparisons with new prognostic factors and treatment programmes.
Mora J, Chan G, Morgenstern D, Amoroso L, Nysom K, Faber J Nat Commun. 2025; 16(1):1636.
PMID: 39952926 PMC: 11828896. DOI: 10.1038/s41467-025-56619-x.
Jahan F, Penna L, Luostarinen A, Veltman L, Hongisto H, Lahteenmaki K Sci Rep. 2024; 14(1):26678.
PMID: 39496674 PMC: 11535237. DOI: 10.1038/s41598-024-76791-2.
Gorostegui M, Munoz J, Perez-Jaume S, Simao-Rafael M, Larrosa C, Garraus M Cancers (Basel). 2024; 16(9).
PMID: 38730688 PMC: 11083939. DOI: 10.3390/cancers16091735.
Mango K, Fekete F, Kiss A, Erdos R, Fekete J, Budi T Sci Rep. 2023; 13(1):11770.
PMID: 37479763 PMC: 10361978. DOI: 10.1038/s41598-023-38983-0.
Puglisi F, Soma R, Podda M, Vetrella S, Rabusin M, Tropia S Front Pediatr. 2022; 10:950911.
PMID: 36405824 PMC: 9673013. DOI: 10.3389/fped.2022.950911.